[tryton-debian-vcs] tryton-modules-health-genetics branch debian created. 4a1f9cbf9ce67a2d6bf3ac710d836e3cabfc380e
Mathias Behrle
tryton-debian-vcs at alioth.debian.org
Fri Feb 27 01:18:25 UTC 2015
The following commit has been merged in the debian branch:
https://alioth.debian.org/plugins/scmgit/cgi-bin/gitweb.cgi/?p=tryton/tryton-modules-health-genetics.git;a=commitdiff;h=4a1f9cbf9ce67a2d6bf3ac710d836e3cabfc380e
commit 4a1f9cbf9ce67a2d6bf3ac710d836e3cabfc380e
Author: Mathias Behrle <mathiasb at m9s.biz>
Date: Sat Feb 21 00:09:04 2015 +0100
Adding upstream version 2.8.1.
Signed-off-by: Mathias Behrle <mathiasb at m9s.biz>
diff --git a/COPYING b/COPYING
new file mode 100644
index 0000000..94a9ed0
--- /dev/null
+++ b/COPYING
@@ -0,0 +1,674 @@
+ GNU GENERAL PUBLIC LICENSE
+ Version 3, 29 June 2007
+
+ Copyright (C) 2007 Free Software Foundation, Inc. <http://fsf.org/>
+ Everyone is permitted to copy and distribute verbatim copies
+ of this license document, but changing it is not allowed.
+
+ Preamble
+
+ The GNU General Public License is a free, copyleft license for
+software and other kinds of works.
+
+ The licenses for most software and other practical works are designed
+to take away your freedom to share and change the works. By contrast,
+the GNU General Public License is intended to guarantee your freedom to
+share and change all versions of a program--to make sure it remains free
+software for all its users. We, the Free Software Foundation, use the
+GNU General Public License for most of our software; it applies also to
+any other work released this way by its authors. You can apply it to
+your programs, too.
+
+ When we speak of free software, we are referring to freedom, not
+price. Our General Public Licenses are designed to make sure that you
+have the freedom to distribute copies of free software (and charge for
+them if you wish), that you receive source code or can get it if you
+want it, that you can change the software or use pieces of it in new
+free programs, and that you know you can do these things.
+
+ To protect your rights, we need to prevent others from denying you
+these rights or asking you to surrender the rights. Therefore, you have
+certain responsibilities if you distribute copies of the software, or if
+you modify it: responsibilities to respect the freedom of others.
+
+ For example, if you distribute copies of such a program, whether
+gratis or for a fee, you must pass on to the recipients the same
+freedoms that you received. You must make sure that they, too, receive
+or can get the source code. And you must show them these terms so they
+know their rights.
+
+ Developers that use the GNU GPL protect your rights with two steps:
+(1) assert copyright on the software, and (2) offer you this License
+giving you legal permission to copy, distribute and/or modify it.
+
+ For the developers' and authors' protection, the GPL clearly explains
+that there is no warranty for this free software. For both users' and
+authors' sake, the GPL requires that modified versions be marked as
+changed, so that their problems will not be attributed erroneously to
+authors of previous versions.
+
+ Some devices are designed to deny users access to install or run
+modified versions of the software inside them, although the manufacturer
+can do so. This is fundamentally incompatible with the aim of
+protecting users' freedom to change the software. The systematic
+pattern of such abuse occurs in the area of products for individuals to
+use, which is precisely where it is most unacceptable. Therefore, we
+have designed this version of the GPL to prohibit the practice for those
+products. If such problems arise substantially in other domains, we
+stand ready to extend this provision to those domains in future versions
+of the GPL, as needed to protect the freedom of users.
+
+ Finally, every program is threatened constantly by software patents.
+States should not allow patents to restrict development and use of
+software on general-purpose computers, but in those that do, we wish to
+avoid the special danger that patents applied to a free program could
+make it effectively proprietary. To prevent this, the GPL assures that
+patents cannot be used to render the program non-free.
+
+ The precise terms and conditions for copying, distribution and
+modification follow.
+
+ TERMS AND CONDITIONS
+
+ 0. Definitions.
+
+ "This License" refers to version 3 of the GNU General Public License.
+
+ "Copyright" also means copyright-like laws that apply to other kinds of
+works, such as semiconductor masks.
+
+ "The Program" refers to any copyrightable work licensed under this
+License. Each licensee is addressed as "you". "Licensees" and
+"recipients" may be individuals or organizations.
+
+ To "modify" a work means to copy from or adapt all or part of the work
+in a fashion requiring copyright permission, other than the making of an
+exact copy. The resulting work is called a "modified version" of the
+earlier work or a work "based on" the earlier work.
+
+ A "covered work" means either the unmodified Program or a work based
+on the Program.
+
+ To "propagate" a work means to do anything with it that, without
+permission, would make you directly or secondarily liable for
+infringement under applicable copyright law, except executing it on a
+computer or modifying a private copy. Propagation includes copying,
+distribution (with or without modification), making available to the
+public, and in some countries other activities as well.
+
+ To "convey" a work means any kind of propagation that enables other
+parties to make or receive copies. Mere interaction with a user through
+a computer network, with no transfer of a copy, is not conveying.
+
+ An interactive user interface displays "Appropriate Legal Notices"
+to the extent that it includes a convenient and prominently visible
+feature that (1) displays an appropriate copyright notice, and (2)
+tells the user that there is no warranty for the work (except to the
+extent that warranties are provided), that licensees may convey the
+work under this License, and how to view a copy of this License. If
+the interface presents a list of user commands or options, such as a
+menu, a prominent item in the list meets this criterion.
+
+ 1. Source Code.
+
+ The "source code" for a work means the preferred form of the work
+for making modifications to it. "Object code" means any non-source
+form of a work.
+
+ A "Standard Interface" means an interface that either is an official
+standard defined by a recognized standards body, or, in the case of
+interfaces specified for a particular programming language, one that
+is widely used among developers working in that language.
+
+ The "System Libraries" of an executable work include anything, other
+than the work as a whole, that (a) is included in the normal form of
+packaging a Major Component, but which is not part of that Major
+Component, and (b) serves only to enable use of the work with that
+Major Component, or to implement a Standard Interface for which an
+implementation is available to the public in source code form. A
+"Major Component", in this context, means a major essential component
+(kernel, window system, and so on) of the specific operating system
+(if any) on which the executable work runs, or a compiler used to
+produce the work, or an object code interpreter used to run it.
+
+ The "Corresponding Source" for a work in object code form means all
+the source code needed to generate, install, and (for an executable
+work) run the object code and to modify the work, including scripts to
+control those activities. However, it does not include the work's
+System Libraries, or general-purpose tools or generally available free
+programs which are used unmodified in performing those activities but
+which are not part of the work. For example, Corresponding Source
+includes interface definition files associated with source files for
+the work, and the source code for shared libraries and dynamically
+linked subprograms that the work is specifically designed to require,
+such as by intimate data communication or control flow between those
+subprograms and other parts of the work.
+
+ The Corresponding Source need not include anything that users
+can regenerate automatically from other parts of the Corresponding
+Source.
+
+ The Corresponding Source for a work in source code form is that
+same work.
+
+ 2. Basic Permissions.
+
+ All rights granted under this License are granted for the term of
+copyright on the Program, and are irrevocable provided the stated
+conditions are met. This License explicitly affirms your unlimited
+permission to run the unmodified Program. The output from running a
+covered work is covered by this License only if the output, given its
+content, constitutes a covered work. This License acknowledges your
+rights of fair use or other equivalent, as provided by copyright law.
+
+ You may make, run and propagate covered works that you do not
+convey, without conditions so long as your license otherwise remains
+in force. You may convey covered works to others for the sole purpose
+of having them make modifications exclusively for you, or provide you
+with facilities for running those works, provided that you comply with
+the terms of this License in conveying all material for which you do
+not control copyright. Those thus making or running the covered works
+for you must do so exclusively on your behalf, under your direction
+and control, on terms that prohibit them from making any copies of
+your copyrighted material outside their relationship with you.
+
+ Conveying under any other circumstances is permitted solely under
+the conditions stated below. Sublicensing is not allowed; section 10
+makes it unnecessary.
+
+ 3. Protecting Users' Legal Rights From Anti-Circumvention Law.
+
+ No covered work shall be deemed part of an effective technological
+measure under any applicable law fulfilling obligations under article
+11 of the WIPO copyright treaty adopted on 20 December 1996, or
+similar laws prohibiting or restricting circumvention of such
+measures.
+
+ When you convey a covered work, you waive any legal power to forbid
+circumvention of technological measures to the extent such circumvention
+is effected by exercising rights under this License with respect to
+the covered work, and you disclaim any intention to limit operation or
+modification of the work as a means of enforcing, against the work's
+users, your or third parties' legal rights to forbid circumvention of
+technological measures.
+
+ 4. Conveying Verbatim Copies.
+
+ You may convey verbatim copies of the Program's source code as you
+receive it, in any medium, provided that you conspicuously and
+appropriately publish on each copy an appropriate copyright notice;
+keep intact all notices stating that this License and any
+non-permissive terms added in accord with section 7 apply to the code;
+keep intact all notices of the absence of any warranty; and give all
+recipients a copy of this License along with the Program.
+
+ You may charge any price or no price for each copy that you convey,
+and you may offer support or warranty protection for a fee.
+
+ 5. Conveying Modified Source Versions.
+
+ You may convey a work based on the Program, or the modifications to
+produce it from the Program, in the form of source code under the
+terms of section 4, provided that you also meet all of these conditions:
+
+ a) The work must carry prominent notices stating that you modified
+ it, and giving a relevant date.
+
+ b) The work must carry prominent notices stating that it is
+ released under this License and any conditions added under section
+ 7. This requirement modifies the requirement in section 4 to
+ "keep intact all notices".
+
+ c) You must license the entire work, as a whole, under this
+ License to anyone who comes into possession of a copy. This
+ License will therefore apply, along with any applicable section 7
+ additional terms, to the whole of the work, and all its parts,
+ regardless of how they are packaged. This License gives no
+ permission to license the work in any other way, but it does not
+ invalidate such permission if you have separately received it.
+
+ d) If the work has interactive user interfaces, each must display
+ Appropriate Legal Notices; however, if the Program has interactive
+ interfaces that do not display Appropriate Legal Notices, your
+ work need not make them do so.
+
+ A compilation of a covered work with other separate and independent
+works, which are not by their nature extensions of the covered work,
+and which are not combined with it such as to form a larger program,
+in or on a volume of a storage or distribution medium, is called an
+"aggregate" if the compilation and its resulting copyright are not
+used to limit the access or legal rights of the compilation's users
+beyond what the individual works permit. Inclusion of a covered work
+in an aggregate does not cause this License to apply to the other
+parts of the aggregate.
+
+ 6. Conveying Non-Source Forms.
+
+ You may convey a covered work in object code form under the terms
+of sections 4 and 5, provided that you also convey the
+machine-readable Corresponding Source under the terms of this License,
+in one of these ways:
+
+ a) Convey the object code in, or embodied in, a physical product
+ (including a physical distribution medium), accompanied by the
+ Corresponding Source fixed on a durable physical medium
+ customarily used for software interchange.
+
+ b) Convey the object code in, or embodied in, a physical product
+ (including a physical distribution medium), accompanied by a
+ written offer, valid for at least three years and valid for as
+ long as you offer spare parts or customer support for that product
+ model, to give anyone who possesses the object code either (1) a
+ copy of the Corresponding Source for all the software in the
+ product that is covered by this License, on a durable physical
+ medium customarily used for software interchange, for a price no
+ more than your reasonable cost of physically performing this
+ conveying of source, or (2) access to copy the
+ Corresponding Source from a network server at no charge.
+
+ c) Convey individual copies of the object code with a copy of the
+ written offer to provide the Corresponding Source. This
+ alternative is allowed only occasionally and noncommercially, and
+ only if you received the object code with such an offer, in accord
+ with subsection 6b.
+
+ d) Convey the object code by offering access from a designated
+ place (gratis or for a charge), and offer equivalent access to the
+ Corresponding Source in the same way through the same place at no
+ further charge. You need not require recipients to copy the
+ Corresponding Source along with the object code. If the place to
+ copy the object code is a network server, the Corresponding Source
+ may be on a different server (operated by you or a third party)
+ that supports equivalent copying facilities, provided you maintain
+ clear directions next to the object code saying where to find the
+ Corresponding Source. Regardless of what server hosts the
+ Corresponding Source, you remain obligated to ensure that it is
+ available for as long as needed to satisfy these requirements.
+
+ e) Convey the object code using peer-to-peer transmission, provided
+ you inform other peers where the object code and Corresponding
+ Source of the work are being offered to the general public at no
+ charge under subsection 6d.
+
+ A separable portion of the object code, whose source code is excluded
+from the Corresponding Source as a System Library, need not be
+included in conveying the object code work.
+
+ A "User Product" is either (1) a "consumer product", which means any
+tangible personal property which is normally used for personal, family,
+or household purposes, or (2) anything designed or sold for incorporation
+into a dwelling. In determining whether a product is a consumer product,
+doubtful cases shall be resolved in favor of coverage. For a particular
+product received by a particular user, "normally used" refers to a
+typical or common use of that class of product, regardless of the status
+of the particular user or of the way in which the particular user
+actually uses, or expects or is expected to use, the product. A product
+is a consumer product regardless of whether the product has substantial
+commercial, industrial or non-consumer uses, unless such uses represent
+the only significant mode of use of the product.
+
+ "Installation Information" for a User Product means any methods,
+procedures, authorization keys, or other information required to install
+and execute modified versions of a covered work in that User Product from
+a modified version of its Corresponding Source. The information must
+suffice to ensure that the continued functioning of the modified object
+code is in no case prevented or interfered with solely because
+modification has been made.
+
+ If you convey an object code work under this section in, or with, or
+specifically for use in, a User Product, and the conveying occurs as
+part of a transaction in which the right of possession and use of the
+User Product is transferred to the recipient in perpetuity or for a
+fixed term (regardless of how the transaction is characterized), the
+Corresponding Source conveyed under this section must be accompanied
+by the Installation Information. But this requirement does not apply
+if neither you nor any third party retains the ability to install
+modified object code on the User Product (for example, the work has
+been installed in ROM).
+
+ The requirement to provide Installation Information does not include a
+requirement to continue to provide support service, warranty, or updates
+for a work that has been modified or installed by the recipient, or for
+the User Product in which it has been modified or installed. Access to a
+network may be denied when the modification itself materially and
+adversely affects the operation of the network or violates the rules and
+protocols for communication across the network.
+
+ Corresponding Source conveyed, and Installation Information provided,
+in accord with this section must be in a format that is publicly
+documented (and with an implementation available to the public in
+source code form), and must require no special password or key for
+unpacking, reading or copying.
+
+ 7. Additional Terms.
+
+ "Additional permissions" are terms that supplement the terms of this
+License by making exceptions from one or more of its conditions.
+Additional permissions that are applicable to the entire Program shall
+be treated as though they were included in this License, to the extent
+that they are valid under applicable law. If additional permissions
+apply only to part of the Program, that part may be used separately
+under those permissions, but the entire Program remains governed by
+this License without regard to the additional permissions.
+
+ When you convey a copy of a covered work, you may at your option
+remove any additional permissions from that copy, or from any part of
+it. (Additional permissions may be written to require their own
+removal in certain cases when you modify the work.) You may place
+additional permissions on material, added by you to a covered work,
+for which you have or can give appropriate copyright permission.
+
+ Notwithstanding any other provision of this License, for material you
+add to a covered work, you may (if authorized by the copyright holders of
+that material) supplement the terms of this License with terms:
+
+ a) Disclaiming warranty or limiting liability differently from the
+ terms of sections 15 and 16 of this License; or
+
+ b) Requiring preservation of specified reasonable legal notices or
+ author attributions in that material or in the Appropriate Legal
+ Notices displayed by works containing it; or
+
+ c) Prohibiting misrepresentation of the origin of that material, or
+ requiring that modified versions of such material be marked in
+ reasonable ways as different from the original version; or
+
+ d) Limiting the use for publicity purposes of names of licensors or
+ authors of the material; or
+
+ e) Declining to grant rights under trademark law for use of some
+ trade names, trademarks, or service marks; or
+
+ f) Requiring indemnification of licensors and authors of that
+ material by anyone who conveys the material (or modified versions of
+ it) with contractual assumptions of liability to the recipient, for
+ any liability that these contractual assumptions directly impose on
+ those licensors and authors.
+
+ All other non-permissive additional terms are considered "further
+restrictions" within the meaning of section 10. If the Program as you
+received it, or any part of it, contains a notice stating that it is
+governed by this License along with a term that is a further
+restriction, you may remove that term. If a license document contains
+a further restriction but permits relicensing or conveying under this
+License, you may add to a covered work material governed by the terms
+of that license document, provided that the further restriction does
+not survive such relicensing or conveying.
+
+ If you add terms to a covered work in accord with this section, you
+must place, in the relevant source files, a statement of the
+additional terms that apply to those files, or a notice indicating
+where to find the applicable terms.
+
+ Additional terms, permissive or non-permissive, may be stated in the
+form of a separately written license, or stated as exceptions;
+the above requirements apply either way.
+
+ 8. Termination.
+
+ You may not propagate or modify a covered work except as expressly
+provided under this License. Any attempt otherwise to propagate or
+modify it is void, and will automatically terminate your rights under
+this License (including any patent licenses granted under the third
+paragraph of section 11).
+
+ However, if you cease all violation of this License, then your
+license from a particular copyright holder is reinstated (a)
+provisionally, unless and until the copyright holder explicitly and
+finally terminates your license, and (b) permanently, if the copyright
+holder fails to notify you of the violation by some reasonable means
+prior to 60 days after the cessation.
+
+ Moreover, your license from a particular copyright holder is
+reinstated permanently if the copyright holder notifies you of the
+violation by some reasonable means, this is the first time you have
+received notice of violation of this License (for any work) from that
+copyright holder, and you cure the violation prior to 30 days after
+your receipt of the notice.
+
+ Termination of your rights under this section does not terminate the
+licenses of parties who have received copies or rights from you under
+this License. If your rights have been terminated and not permanently
+reinstated, you do not qualify to receive new licenses for the same
+material under section 10.
+
+ 9. Acceptance Not Required for Having Copies.
+
+ You are not required to accept this License in order to receive or
+run a copy of the Program. Ancillary propagation of a covered work
+occurring solely as a consequence of using peer-to-peer transmission
+to receive a copy likewise does not require acceptance. However,
+nothing other than this License grants you permission to propagate or
+modify any covered work. These actions infringe copyright if you do
+not accept this License. Therefore, by modifying or propagating a
+covered work, you indicate your acceptance of this License to do so.
+
+ 10. Automatic Licensing of Downstream Recipients.
+
+ Each time you convey a covered work, the recipient automatically
+receives a license from the original licensors, to run, modify and
+propagate that work, subject to this License. You are not responsible
+for enforcing compliance by third parties with this License.
+
+ An "entity transaction" is a transaction transferring control of an
+organization, or substantially all assets of one, or subdividing an
+organization, or merging organizations. If propagation of a covered
+work results from an entity transaction, each party to that
+transaction who receives a copy of the work also receives whatever
+licenses to the work the party's predecessor in interest had or could
+give under the previous paragraph, plus a right to possession of the
+Corresponding Source of the work from the predecessor in interest, if
+the predecessor has it or can get it with reasonable efforts.
+
+ You may not impose any further restrictions on the exercise of the
+rights granted or affirmed under this License. For example, you may
+not impose a license fee, royalty, or other charge for exercise of
+rights granted under this License, and you may not initiate litigation
+(including a cross-claim or counterclaim in a lawsuit) alleging that
+any patent claim is infringed by making, using, selling, offering for
+sale, or importing the Program or any portion of it.
+
+ 11. Patents.
+
+ A "contributor" is a copyright holder who authorizes use under this
+License of the Program or a work on which the Program is based. The
+work thus licensed is called the contributor's "contributor version".
+
+ A contributor's "essential patent claims" are all patent claims
+owned or controlled by the contributor, whether already acquired or
+hereafter acquired, that would be infringed by some manner, permitted
+by this License, of making, using, or selling its contributor version,
+but do not include claims that would be infringed only as a
+consequence of further modification of the contributor version. For
+purposes of this definition, "control" includes the right to grant
+patent sublicenses in a manner consistent with the requirements of
+this License.
+
+ Each contributor grants you a non-exclusive, worldwide, royalty-free
+patent license under the contributor's essential patent claims, to
+make, use, sell, offer for sale, import and otherwise run, modify and
+propagate the contents of its contributor version.
+
+ In the following three paragraphs, a "patent license" is any express
+agreement or commitment, however denominated, not to enforce a patent
+(such as an express permission to practice a patent or covenant not to
+sue for patent infringement). To "grant" such a patent license to a
+party means to make such an agreement or commitment not to enforce a
+patent against the party.
+
+ If you convey a covered work, knowingly relying on a patent license,
+and the Corresponding Source of the work is not available for anyone
+to copy, free of charge and under the terms of this License, through a
+publicly available network server or other readily accessible means,
+then you must either (1) cause the Corresponding Source to be so
+available, or (2) arrange to deprive yourself of the benefit of the
+patent license for this particular work, or (3) arrange, in a manner
+consistent with the requirements of this License, to extend the patent
+license to downstream recipients. "Knowingly relying" means you have
+actual knowledge that, but for the patent license, your conveying the
+covered work in a country, or your recipient's use of the covered work
+in a country, would infringe one or more identifiable patents in that
+country that you have reason to believe are valid.
+
+ If, pursuant to or in connection with a single transaction or
+arrangement, you convey, or propagate by procuring conveyance of, a
+covered work, and grant a patent license to some of the parties
+receiving the covered work authorizing them to use, propagate, modify
+or convey a specific copy of the covered work, then the patent license
+you grant is automatically extended to all recipients of the covered
+work and works based on it.
+
+ A patent license is "discriminatory" if it does not include within
+the scope of its coverage, prohibits the exercise of, or is
+conditioned on the non-exercise of one or more of the rights that are
+specifically granted under this License. You may not convey a covered
+work if you are a party to an arrangement with a third party that is
+in the business of distributing software, under which you make payment
+to the third party based on the extent of your activity of conveying
+the work, and under which the third party grants, to any of the
+parties who would receive the covered work from you, a discriminatory
+patent license (a) in connection with copies of the covered work
+conveyed by you (or copies made from those copies), or (b) primarily
+for and in connection with specific products or compilations that
+contain the covered work, unless you entered into that arrangement,
+or that patent license was granted, prior to 28 March 2007.
+
+ Nothing in this License shall be construed as excluding or limiting
+any implied license or other defenses to infringement that may
+otherwise be available to you under applicable patent law.
+
+ 12. No Surrender of Others' Freedom.
+
+ If conditions are imposed on you (whether by court order, agreement or
+otherwise) that contradict the conditions of this License, they do not
+excuse you from the conditions of this License. If you cannot convey a
+covered work so as to satisfy simultaneously your obligations under this
+License and any other pertinent obligations, then as a consequence you may
+not convey it at all. For example, if you agree to terms that obligate you
+to collect a royalty for further conveying from those to whom you convey
+the Program, the only way you could satisfy both those terms and this
+License would be to refrain entirely from conveying the Program.
+
+ 13. Use with the GNU Affero General Public License.
+
+ Notwithstanding any other provision of this License, you have
+permission to link or combine any covered work with a work licensed
+under version 3 of the GNU Affero General Public License into a single
+combined work, and to convey the resulting work. The terms of this
+License will continue to apply to the part which is the covered work,
+but the special requirements of the GNU Affero General Public License,
+section 13, concerning interaction through a network will apply to the
+combination as such.
+
+ 14. Revised Versions of this License.
+
+ The Free Software Foundation may publish revised and/or new versions of
+the GNU General Public License from time to time. Such new versions will
+be similar in spirit to the present version, but may differ in detail to
+address new problems or concerns.
+
+ Each version is given a distinguishing version number. If the
+Program specifies that a certain numbered version of the GNU General
+Public License "or any later version" applies to it, you have the
+option of following the terms and conditions either of that numbered
+version or of any later version published by the Free Software
+Foundation. If the Program does not specify a version number of the
+GNU General Public License, you may choose any version ever published
+by the Free Software Foundation.
+
+ If the Program specifies that a proxy can decide which future
+versions of the GNU General Public License can be used, that proxy's
+public statement of acceptance of a version permanently authorizes you
+to choose that version for the Program.
+
+ Later license versions may give you additional or different
+permissions. However, no additional obligations are imposed on any
+author or copyright holder as a result of your choosing to follow a
+later version.
+
+ 15. Disclaimer of Warranty.
+
+ THERE IS NO WARRANTY FOR THE PROGRAM, TO THE EXTENT PERMITTED BY
+APPLICABLE LAW. EXCEPT WHEN OTHERWISE STATED IN WRITING THE COPYRIGHT
+HOLDERS AND/OR OTHER PARTIES PROVIDE THE PROGRAM "AS IS" WITHOUT WARRANTY
+OF ANY KIND, EITHER EXPRESSED OR IMPLIED, INCLUDING, BUT NOT LIMITED TO,
+THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR
+PURPOSE. THE ENTIRE RISK AS TO THE QUALITY AND PERFORMANCE OF THE PROGRAM
+IS WITH YOU. SHOULD THE PROGRAM PROVE DEFECTIVE, YOU ASSUME THE COST OF
+ALL NECESSARY SERVICING, REPAIR OR CORRECTION.
+
+ 16. Limitation of Liability.
+
+ IN NO EVENT UNLESS REQUIRED BY APPLICABLE LAW OR AGREED TO IN WRITING
+WILL ANY COPYRIGHT HOLDER, OR ANY OTHER PARTY WHO MODIFIES AND/OR CONVEYS
+THE PROGRAM AS PERMITTED ABOVE, BE LIABLE TO YOU FOR DAMAGES, INCLUDING ANY
+GENERAL, SPECIAL, INCIDENTAL OR CONSEQUENTIAL DAMAGES ARISING OUT OF THE
+USE OR INABILITY TO USE THE PROGRAM (INCLUDING BUT NOT LIMITED TO LOSS OF
+DATA OR DATA BEING RENDERED INACCURATE OR LOSSES SUSTAINED BY YOU OR THIRD
+PARTIES OR A FAILURE OF THE PROGRAM TO OPERATE WITH ANY OTHER PROGRAMS),
+EVEN IF SUCH HOLDER OR OTHER PARTY HAS BEEN ADVISED OF THE POSSIBILITY OF
+SUCH DAMAGES.
+
+ 17. Interpretation of Sections 15 and 16.
+
+ If the disclaimer of warranty and limitation of liability provided
+above cannot be given local legal effect according to their terms,
+reviewing courts shall apply local law that most closely approximates
+an absolute waiver of all civil liability in connection with the
+Program, unless a warranty or assumption of liability accompanies a
+copy of the Program in return for a fee.
+
+ END OF TERMS AND CONDITIONS
+
+ How to Apply These Terms to Your New Programs
+
+ If you develop a new program, and you want it to be of the greatest
+possible use to the public, the best way to achieve this is to make it
+free software which everyone can redistribute and change under these terms.
+
+ To do so, attach the following notices to the program. It is safest
+to attach them to the start of each source file to most effectively
+state the exclusion of warranty; and each file should have at least
+the "copyright" line and a pointer to where the full notice is found.
+
+ <one line to give the program's name and a brief idea of what it does.>
+ Copyright (C) <year> <name of author>
+
+ This program is free software: you can redistribute it and/or modify
+ it under the terms of the GNU General Public License as published by
+ the Free Software Foundation, either version 3 of the License, or
+ (at your option) any later version.
+
+ This program is distributed in the hope that it will be useful,
+ but WITHOUT ANY WARRANTY; without even the implied warranty of
+ MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the
+ GNU General Public License for more details.
+
+ You should have received a copy of the GNU General Public License
+ along with this program. If not, see <http://www.gnu.org/licenses/>.
+
+Also add information on how to contact you by electronic and paper mail.
+
+ If the program does terminal interaction, make it output a short
+notice like this when it starts in an interactive mode:
+
+ <program> Copyright (C) <year> <name of author>
+ This program comes with ABSOLUTELY NO WARRANTY; for details type `show w'.
+ This is free software, and you are welcome to redistribute it
+ under certain conditions; type `show c' for details.
+
+The hypothetical commands `show w' and `show c' should show the appropriate
+parts of the General Public License. Of course, your program's commands
+might be different; for a GUI interface, you would use an "about box".
+
+ You should also get your employer (if you work as a programmer) or school,
+if any, to sign a "copyright disclaimer" for the program, if necessary.
+For more information on this, and how to apply and follow the GNU GPL, see
+<http://www.gnu.org/licenses/>.
+
+ The GNU General Public License does not permit incorporating your program
+into proprietary programs. If your program is a subroutine library, you
+may consider it more useful to permit linking proprietary applications with
+the library. If this is what you want to do, use the GNU Lesser General
+Public License instead of this License. But first, please read
+<http://www.gnu.org/philosophy/why-not-lgpl.html>.
diff --git a/MANIFEST.in b/MANIFEST.in
new file mode 100644
index 0000000..f7edfb1
--- /dev/null
+++ b/MANIFEST.in
@@ -0,0 +1 @@
+global-include *.xml *.odt *.svg *.po *.rst README COPYING
diff --git a/PKG-INFO b/PKG-INFO
new file mode 100644
index 0000000..68563fc
--- /dev/null
+++ b/PKG-INFO
@@ -0,0 +1,23 @@
+Metadata-Version: 1.1
+Name: trytond_health_genetics
+Version: 2.8.1
+Summary: GNU Health Genetics Module
+Home-page: http://health.gnu.org/
+Author: GNU Solidario
+Author-email: health at gnusolidario.org
+License: GPL-3
+Download-URL: http://ftp.gnu.org/gnu/health/
+Description: UNKNOWN
+Platform: UNKNOWN
+Classifier: Development Status :: 5 - Production/Stable
+Classifier: Environment :: Plugins
+Classifier: Framework :: Tryton
+Classifier: Intended Audience :: Developers
+Classifier: Intended Audience :: Healthcare Industry
+Classifier: License :: OSI Approved :: GNU General Public License (GPL)
+Classifier: Natural Language :: English
+Classifier: Natural Language :: Spanish
+Classifier: Operating System :: OS Independent
+Classifier: Programming Language :: Python :: 2.7
+Classifier: Topic :: Scientific/Engineering :: Bio-Informatics
+Classifier: Topic :: Scientific/Engineering :: Medical Science Apps.
diff --git a/README b/README
new file mode 100644
index 0000000..4d62bf1
--- /dev/null
+++ b/README
@@ -0,0 +1,22 @@
+# Copyright (C) 2008-2015 Luis Falcon
+
+# This program is free software: you can redistribute it and/or modify
+# it under the terms of the GNU General Public License as published by
+# the Free Software Foundation, either version 3 of the License, or
+# (at your option) any later version.
+
+# This program is distributed in the hope that it will be useful,
+# but WITHOUT ANY WARRANTY; without even the implied warranty of
+# MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the
+# GNU General Public License for more details.
+
+# You should have received a copy of the GNU General Public License
+# along with this program. If not, see <http://www.gnu.org/licenses/>.
+
+
+Please read the README file at the main "health" module
+
+For more information, please visit :
+http://health.gnu.org
+email : health at gnusolidario.org
+
diff --git a/__init__.py b/__init__.py
new file mode 100644
index 0000000..08d2c35
--- /dev/null
+++ b/__init__.py
@@ -0,0 +1,34 @@
+# -*- coding: utf-8 -*-
+##############################################################################
+#
+# GNU Health: The Free Health and Hospital Information System
+# Copyright (C) 2008-2015 Luis Falcon <lfalcon at gnusolidario.org>
+# Copyright (C) 2011-2015 GNU Solidario <health at gnusolidario.org>
+#
+#
+# This program is free software: you can redistribute it and/or modify
+# it under the terms of the GNU General Public License as published by
+# the Free Software Foundation, either version 3 of the License, or
+# (at your option) any later version.
+#
+# This program is distributed in the hope that it will be useful,
+# but WITHOUT ANY WARRANTY; without even the implied warranty of
+# MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the
+# GNU General Public License for more details.
+#
+# You should have received a copy of the GNU General Public License
+# along with this program. If not, see <http://www.gnu.org/licenses/>.
+#
+##############################################################################
+
+from trytond.pool import Pool
+from .health_genetics import *
+
+
+def register():
+ Pool.register(
+ DiseaseGene,
+ PatientGeneticRisk,
+ FamilyDiseases,
+ GnuHealthPatient,
+ module='health_genetics', type_='model')
diff --git a/data/disease_genes.xml b/data/disease_genes.xml
new file mode 100644
index 0000000..20db8f8
--- /dev/null
+++ b/data/disease_genes.xml
@@ -0,0 +1,36164 @@
+<?xml version="1.0" encoding="utf-8" ?>
+<tryton>
+<data noupdate="1" skiptest="1">
+<record model="gnuhealth.disease.gene" id="A2BP1">
+ <field name="name">A2BP1</field>
+ <field name="long_name">ataxin 2-binding protein 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="A2M">
+ <field name="name">A2M</field>
+ <field name="long_name">alpha-2-macroglobulin</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.3-p12.3</field>
+ <field name="info">
+Emphysema due to alpha-2-macroglobulin deficiency
+Alzheimer disease, susceptibility to [MIM:104300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="A4GALT">
+ <field name="name">A4GALT</field>
+ <field name="long_name">alpha 1,4-galactosyltransferase</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.2</field>
+ <field name="info">
+Blood group, P system [MIM:111400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AA1">
+ <field name="name">AA1</field>
+ <field name="long_name">Alopecia areata 1</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.3-p11.2</field>
+ <field name="info">
+Alopecia areata 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AA2">
+ <field name="name">AA2</field>
+ <field name="long_name">Alopecia areata 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q11-q22</field>
+ <field name="info">
+Alopecia areata 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AAA3">
+ <field name="name">AAA3</field>
+ <field name="long_name">Aneurysm, familial abdominal 3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21</field>
+ <field name="info">
+Aneurysm, familial abdominal 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AAAS">
+ <field name="name">AAAS</field>
+ <field name="long_name">achalasia, adrenocortical insufficiency, alacrimia (Allgrove, triple-A)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Achalasia-addisonianism-alacrimia syndrome [MIM:231550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AANAT">
+ <field name="name">AANAT</field>
+ <field name="long_name">arylalkylamine N-acetyltransferase</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+Delayed sleep phase syndrome, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AARS">
+ <field name="name">AARS</field>
+ <field name="long_name">alanyl-tRNA synthetase</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AASS">
+ <field name="name">AASS</field>
+ <field name="long_name">aminoadipate-semialdehyde synthase</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31.3</field>
+ <field name="info">
+Hyperlysinemia [MIM:238700]
+Saccharopinuria [MIM:268700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AAT2">
+ <field name="name">AAT2</field>
+ <field name="long_name">Aortic aneurysm, familial thoracic 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13-q14</field>
+ <field name="info">
+Aortic aneurysm, familial thoracic 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABAT">
+ <field name="name">ABAT</field>
+ <field name="long_name">4-aminobutyrate aminotransferase</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+GABA-transaminase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCA12">
+ <field name="name">ABCA12</field>
+ <field name="long_name">ATP-binding cassette, sub-family A (ABC1), member 12</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q34</field>
+ <field name="info">
+Ichthyosis, lamellar 2 [MIM:601277]
+Ichthyosis, harlequin [MIM:242500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCA1">
+ <field name="name">ABCA1</field>
+ <field name="long_name">ATP-binding cassette, sub-family A (ABC1), member 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22-q31</field>
+ <field name="info">
+Tangier disease [MIM:205400]
+HDL deficiency, type 2 [MIM:604091]
+Coronary artery disease in familial hypercholesterolemia, protection against [MIM:143890]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCA3">
+ <field name="name">ABCA3</field>
+ <field name="long_name">ATP-binding cassette, sub-family A (ABC1), member 3</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+Surfactant metabolism dysfunction, pulmonary, 3 [MIM:610921]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCA4">
+ <field name="name">ABCA4</field>
+ <field name="long_name">ATP-binding cassette, sub-family A (ABC1), member 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p21-p13</field>
+ <field name="info">
+Stargardt disease-1 [MIM:248200]
+Retinitis pigmentosa-19 [MIM:601718]
+Cone-rod dystrophy 3 [MIM:604116]
+Macular degeneration, age-related, 2 [MIM:153800]
+Fundus flavimaculatus [MIM:248200]
+Retinal dystrophy, early-onset severe [MIM:248200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCB11">
+ <field name="name">ABCB11</field>
+ <field name="long_name">ATP-binding cassette, sub-family B (MDR/TAP), member 11</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q24</field>
+ <field name="info">
+Cholestasis, progressive familial intrahepatic 2 [MIM:601847]
+Cholestasis, benign recurrent intrahepatic, 2 [MIM:605479]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCB1">
+ <field name="name">ABCB1</field>
+ <field name="long_name">ATP-binding cassette, sub-family B (MDR/TAP), member 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.1</field>
+ <field name="info">
+Colchicine resistance
+Inflammatory bowel disease 13, susceptibility to [MIM:612244]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCB4">
+ <field name="name">ABCB4</field>
+ <field name="long_name">ATP-binding cassette, sub-family B (MDR/TAP), member 4</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.1</field>
+ <field name="info">
+Cholestasis, progressive familial intrahepatic 3 [MIM:602347]
+Cholestasis, familial intrahepatic, of pregnancy [MIM:147480]
+Gallbladder disease 1 [MIM:600803]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCB7">
+ <field name="name">ABCB7</field>
+ <field name="long_name">ATP-binding cassette, sub-family B (MDR/TAP), member 7</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.1-q13.3</field>
+ <field name="info">
+Anemia, sideroblastic, with ataxia [MIM:301310]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCC11">
+ <field name="name">ABCC11</field>
+ <field name="long_name">ATP-binding cassette, sub-family C (CFTR/MRP), member 11</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q12.1</field>
+ <field name="info">
+Earwax, wet/dry [MIM:117800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCC1">
+ <field name="name">ABCC1</field>
+ <field name="long_name">ATP-binding cassette, sub-family C (CFTR/MRP), member 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCC2">
+ <field name="name">ABCC2</field>
+ <field name="long_name">ATP-binding cassette, sub-family C (CFTR/MRP), member 2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+Dubin-Johnson syndrome [MIM:237500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCC3">
+ <field name="name">ABCC3</field>
+ <field name="long_name">ATP-binding cassette, sub-family C (CFTR/MRP), member 3</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCC4">
+ <field name="name">ABCC4</field>
+ <field name="long_name">ATP-binding cassette, sub-family C (CFTR/MRP), member 4</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCC6">
+ <field name="name">ABCC6</field>
+ <field name="long_name">ATP-binding cassette, sub-family C (CFTR/MRP), member 6</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.1</field>
+ <field name="info">
+Pseudoxanthoma elasticum [MIM:264800]
+Pseudoxanthoma elasticum, forme fruste [MIM:177850]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCC8">
+ <field name="name">ABCC8</field>
+ <field name="long_name">ATP-binding cassette, sub-family C (CFTR/MRP), member 8</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.1</field>
+ <field name="info">
+Hyperinsulinemic hypoglycemia, familial, 1 [MIM:256450]
+Hypoglycemia of infancy, leucine-sensitive [MIM:240800]
+Diabetes mellitus, transient neonatal 2 [MIM:610374]
+Diabetes mellitus, noninsulin-dependent [MIM:125853]
+Diabetes mellitus, permanent neonatal [MIM:606176]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCC9">
+ <field name="name">ABCC9</field>
+ <field name="long_name">ATP-binding cassette, sub-family C (CFTR/MRP), member 9</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p12.1</field>
+ <field name="info">
+Cardiomyopathy, dilated, 1O [MIM:608569]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCD1">
+ <field name="name">ABCD1</field>
+ <field name="long_name">ATP-binding cassette, sub-family D (ALD), member 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Adrenoleukodystrophy [MIM:300100]
+Adrenomyeloneuropathy [MIM:300100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCD3">
+ <field name="name">ABCD3</field>
+ <field name="long_name">ATP-binding cassette, sub-family D (ALD), member 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p22-p21</field>
+ <field name="info">
+Zellweger syndrome-2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCG2">
+ <field name="name">ABCG2</field>
+ <field name="long_name">ATP-binding cassette, sub-family G (WHITE), member 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCG5">
+ <field name="name">ABCG5</field>
+ <field name="long_name">ATP-binding cassette, sub-family G (WHITE), member 5</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p21</field>
+ <field name="info">
+Sitosterolemia [MIM:210250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABCG8">
+ <field name="name">ABCG8</field>
+ <field name="long_name">ATP-binding cassette, sub-family G (WHITE), member 8</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p21</field>
+ <field name="info">
+Sitosterolemia [MIM:210250]
+Gallbladder disease 4 [MIM:611465]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABHD5">
+ <field name="name">ABHD5</field>
+ <field name="long_name">abhydrolase domain containing 5</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21</field>
+ <field name="info">
+Chanarin-Dorfman syndrome [MIM:275630]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABL1">
+ <field name="name">ABL1</field>
+ <field name="long_name">c-abl oncogene 1, receptor tyrosine kinase</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.1</field>
+ <field name="info">
+Leukemia, Philadelphia chromosome-positive, resistant to imatinib</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABL2">
+ <field name="name">ABL2</field>
+ <field name="long_name">v-abl Abelson murine leukemia viral oncogene homolog 2 (arg, Abelson-related gene)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q24-q25</field>
+ <field name="info">
+Leukemia, acute myeloid, with eosinophilia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABO">
+ <field name="name">ABO</field>
+ <field name="long_name">ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+Blood group, ABO system</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ABP1">
+ <field name="name">ABP1</field>
+ <field name="long_name">amiloride binding protein 1 (amine oxidase (copper-containing))</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31-q32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACAA1">
+ <field name="name">ACAA1</field>
+ <field name="long_name">acetyl-Coenzyme A acyltransferase 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p23-p22</field>
+ <field name="info">
+Pseudo-Zellweger syndrome [MIM:261515]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACACA">
+ <field name="name">ACACA</field>
+ <field name="long_name">acetyl-Coenzyme A carboxylase alpha</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+Acetyl-CoA carboxylase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACAD8">
+ <field name="name">ACAD8</field>
+ <field name="long_name">acyl-Coenzyme A dehydrogenase family, member 8</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q25</field>
+ <field name="info">
+Isobutyryl-CoA dehydrogenase deficiency [MIM:611283]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACAD9">
+ <field name="name">ACAD9</field>
+ <field name="long_name">acyl-Coenzyme A dehydrogenase family, member 9</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26</field>
+ <field name="info">
+ACAD9 deficiency [MIM:611126]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACADL">
+ <field name="name">ACADL</field>
+ <field name="long_name">acyl-Coenzyme A dehydrogenase, long chain</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q34-q35</field>
+ <field name="info">
+Acyl-CoA dehydrogenase, long chain, deficiency of [MIM:201460]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACADM">
+ <field name="name">ACADM</field>
+ <field name="long_name">acyl-Coenzyme A dehydrogenase, C-4 to C-12 straight chain</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+Acyl-CoA dehydrogenase, medium chain, deficiency of [MIM:201450]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACADSB">
+ <field name="name">ACADSB</field>
+ <field name="long_name">acyl-Coenzyme A dehydrogenase, short/branched chain</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q25-q26</field>
+ <field name="info">
+2-methylbutyrylglycinuria [MIM:610006]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACADS">
+ <field name="name">ACADS</field>
+ <field name="long_name">acyl-Coenzyme A dehydrogenase, C-2 to C-3 short chain</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q22-qter</field>
+ <field name="info">
+Acyl-CoA dehydrogenase, short-chain, deficiency of [MIM:201470]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACADVL">
+ <field name="name">ACADVL</field>
+ <field name="long_name">acyl-Coenzyme A dehydrogenase, very long chain</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13</field>
+ <field name="info">
+VLCAD deficiency [MIM:201475]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACAN">
+ <field name="name">ACAN</field>
+ <field name="long_name">aggrecan</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26.1</field>
+ <field name="info">
+Spondyloepiphyseal dysplasia, Kimberley type [MIM:608361]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACAT1">
+ <field name="name">ACAT1</field>
+ <field name="long_name">acetyl-Coenzyme A acetyltransferase 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22.3-q23.1</field>
+ <field name="info">
+Alpha-methylacetoacetic aciduria [MIM:203750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACAT2">
+ <field name="name">ACAT2</field>
+ <field name="long_name">acetyl-Coenzyme A acetyltransferase 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25.3-q26</field>
+ <field name="info">
+ACAT2 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACCN3">
+ <field name="name">ACCN3</field>
+ <field name="long_name">amiloride-sensitive cation channel 3</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q35</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACE">
+ <field name="name">ACE</field>
+ <field name="long_name">angiotensin I converting enzyme (peptidyl-dipeptidase A) 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23</field>
+ <field name="info">
+Myocardial infarction, susceptibility to
+Alzheimer disease, susceptibility to [MIM:104300]
+Microvascular complications of diabetes 3 [MIM:612624]
+Angiotensin I-converting enzyme, benign serum increase
+SARS, progression of
+Renal tubular dysgenesis [MIM:267430]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACF">
+ <field name="name">ACF</field>
+ <field name="long_name">Asymmetric crying facies (Cayler cardiofacial syndrome)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11</field>
+ <field name="info">
+Cayler cardiofacial syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACHE">
+ <field name="name">ACHE</field>
+ <field name="long_name">acetylcholinesterase (Yt blood group)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22</field>
+ <field name="info">
+Blood group, Yt system [MIM:112100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACHM1">
+ <field name="name">ACHM1</field>
+ <field name="long_name">achromatopsia (rod monochromacy) 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21-q22</field>
+ <field name="info">
+Achromatopsia-3 [MIM:262300]
+Macular degeneration, juvenile [MIM:248200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACLS">
+ <field name="name">ACLS</field>
+ <field name="long_name">acrocallosal syndrome</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p13</field>
+ <field name="info">
+Greig cephalopolysyndactyly syndrome [MIM:175700]
+Pallister-Hall syndrome [MIM:146510]
+Polydactyly, preaxial, type IV [MIM:174700]
+Polydactyly, postaxial, types A1 and B [MIM:174200]
+Acrocallosal syndrome [MIM:200990]
+Hypothalamic hamartomas, somatic [MIM:241800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACOX1">
+ <field name="name">ACOX1</field>
+ <field name="long_name">acyl-Coenzyme A oxidase 1, palmitoyl</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+Peroxisomal acyl-CoA oxidase deficiency [MIM:264470]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACP2">
+ <field name="name">ACP2</field>
+ <field name="long_name">acid phosphatase 2, lysosomal</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p12-p11</field>
+ <field name="info">
+Lysosomal acid phosphatase deficiency [MIM:200950]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACRPS">
+ <field name="name">ACRPS</field>
+ <field name="long_name">Acropectoral syndrome</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q36</field>
+ <field name="info">
+Acropectoral syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACRPV">
+ <field name="name">ACRPV</field>
+ <field name="long_name">Acropectorovertebral dysplasia (F syndrome)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q36</field>
+ <field name="info">
+Acropectorovertebral dysplasia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACR">
+ <field name="name">ACR</field>
+ <field name="long_name">acrosin</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.3</field>
+ <field name="info">
+Male infertility due to acrosin deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACSL4">
+ <field name="name">ACSL4</field>
+ <field name="long_name">acyl-CoA synthetase long-chain family member 4</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22.3</field>
+ <field name="info">
+Mental retardation, X-linked nonspecific, 63 [MIM:300387]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACSL6">
+ <field name="name">ACSL6</field>
+ <field name="long_name">acyl-CoA synthetase long-chain family member 6</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Myelodysplastic syndrome
+Myelogenous leukemia, acute</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACSM3">
+ <field name="name">ACSM3</field>
+ <field name="long_name">acyl-CoA synthetase medium-chain family member 3</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.11</field>
+ <field name="info">
+Hypertension, essential</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACTA1">
+ <field name="name">ACTA1</field>
+ <field name="long_name">actin, alpha 1, skeletal muscle</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42.1</field>
+ <field name="info">
+Myopathy, nemaline, 3 [MIM:161800]
+Myopathy, actin, congenital, with excess of thin myofilaments [MIM:161800]
+Myopathy, actin, congenital, with cores
+Myopathy, congenital, with fiber-type disporportion 1 [MIM:255310]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACTA2">
+ <field name="name">ACTA2</field>
+ <field name="long_name">actin, alpha 2, smooth muscle, aorta</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22-q24</field>
+ <field name="info">
+Aortic aneurysm, familial thoracic 6 [MIM:611788]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACTB">
+ <field name="name">ACTB</field>
+ <field name="long_name">actin, beta</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p22-p12</field>
+ <field name="info">
+Dystonia, juvenile-onset [MIM:607371]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACTC1">
+ <field name="name">ACTC1</field>
+ <field name="long_name">actin, alpha, cardiac muscle 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q14</field>
+ <field name="info">
+Cardiomyopathy, dilated, 1R
+Cardiomyopathy, familial hypertrophic, 11 [MIM:612098]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACTD">
+ <field name="name">ACTD</field>
+ <field name="long_name">Acetabular dysplasia</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q22</field>
+ <field name="info">
+Acetabular dysplasia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACTG1">
+ <field name="name">ACTG1</field>
+ <field name="long_name">actin, gamma 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25.3</field>
+ <field name="info">
+Deafness, autosomal dominant 20/26 [MIM:604717]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACTN2">
+ <field name="name">ACTN2</field>
+ <field name="long_name">actinin, alpha 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42-q43</field>
+ <field name="info">
+Cardiomyopathy, dilated, 1AA [MIM:612158]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACTN3">
+ <field name="name">ACTN3</field>
+ <field name="long_name">actinin, alpha 3</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13-q14</field>
+ <field name="info">
+Alpha-actinin-3 deficiency
+Sprinting performance</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACTN4">
+ <field name="name">ACTN4</field>
+ <field name="long_name">actinin, alpha 4</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+Glomerulosclerosis, focal segmental, 1 [MIM:603278]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACVR1B">
+ <field name="name">ACVR1B</field>
+ <field name="long_name">activin A receptor, type IB</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Pancreatic cancer, somatic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACVR1">
+ <field name="name">ACVR1</field>
+ <field name="long_name">activin A receptor, type I</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q23-q24</field>
+ <field name="info">
+Fibrodysplasia ossificans progressiva [MIM:135100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACVR2B">
+ <field name="name">ACVR2B</field>
+ <field name="long_name">activin A receptor, type IIB</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p22-p21.3</field>
+ <field name="info">
+Heterotaxy, visceral, 4, autosomal</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACVRL1">
+ <field name="name">ACVRL1</field>
+ <field name="long_name">activin A receptor type II-like 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q11-q14</field>
+ <field name="info">
+Hereditary hemorrhagic telangiectasia-2 [MIM:600376]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ACY1">
+ <field name="name">ACY1</field>
+ <field name="long_name">aminoacylase 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.1</field>
+ <field name="info">
+Aminoacylase 1 deficiency [MIM:609924]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AD10">
+ <field name="name">AD10</field>
+ <field name="long_name">Alzheimer disease-10</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q36</field>
+ <field name="info">
+Alzheimer disease-10 [MIM:104300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AD11">
+ <field name="name">AD11</field>
+ <field name="long_name">Alzheimer disease-11</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p22.1</field>
+ <field name="info">
+Alzheimer disease-11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AD12">
+ <field name="name">AD12</field>
+ <field name="long_name">Alzheimer disease 12</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p12-q22</field>
+ <field name="info">
+Alzheimer disease 12</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AD13">
+ <field name="name">AD13</field>
+ <field name="long_name">Alzheimer disease-13</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Alzheimer disease-13</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AD14">
+ <field name="name">AD14</field>
+ <field name="long_name">Alzheimer disease 14</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q25</field>
+ <field name="info">
+Alzheimer disease-14</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AD15">
+ <field name="name">AD15</field>
+ <field name="long_name">Alzheimer disease-15</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q22-q24</field>
+ <field name="info">
+Alzheimer disease-15</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AD16">
+ <field name="name">AD16</field>
+ <field name="long_name">Alzheimer disease 16</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq21.3</field>
+ <field name="info">
+Alzheimer disease 16</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AD5">
+ <field name="name">AD5</field>
+ <field name="long_name">Alzheimer disease 5</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p11.23-q13.12</field>
+ <field name="info">
+Alzheimer disease-5 [MIM:104300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AD6">
+ <field name="name">AD6</field>
+ <field name="long_name">Alzheimer disease 6</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+Alzheimer disease 6 [MIM:104300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AD7">
+ <field name="name">AD7</field>
+ <field name="long_name">Alzheimer disease 7</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p13</field>
+ <field name="info">
+Alzheimer disease-7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AD8">
+ <field name="name">AD8</field>
+ <field name="long_name">Alzheimer disease 8</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p</field>
+ <field name="info">
+Alzheimer disease 8 [MIM:104300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AD9">
+ <field name="name">AD9</field>
+ <field name="long_name">Alzheimer disease 9</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2</field>
+ <field name="info">
+Alzheimer disease 9, late onset, susceptibility to [MIM:104300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADAMTS10">
+ <field name="name">ADAMTS10</field>
+ <field name="long_name">ADAM metallopeptidase with thrombospondin type 1 motif, 10</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3-p13.2</field>
+ <field name="info">
+Weill-Marchesani syndrome, recessive [MIM:277600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADAMTS13">
+ <field name="name">ADAMTS13</field>
+ <field name="long_name">ADAM metallopeptidase with thrombospondin type 1 motif, 13</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+Thrombotic thrombocytopenic purpura, familial [MIM:274150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADAMTS2">
+ <field name="name">ADAMTS2</field>
+ <field name="long_name">ADAM metallopeptidase with thrombospondin type 1 motif, 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q23</field>
+ <field name="info">
+Ehlers-Danlos syndrome, type VIIC [MIM:225410]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADAMTSL2">
+ <field name="name">ADAMTSL2</field>
+ <field name="long_name">ADAMTS-like 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.2</field>
+ <field name="info">
+Geleophysic dysplasia [MIM:231050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADAMTSL4">
+ <field name="name">ADAMTSL4</field>
+ <field name="long_name">ADAMTS-like 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Ectopia lentis, isolated, autosomal recessive [MIM:225100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADAR">
+ <field name="name">ADAR</field>
+ <field name="long_name">adenosine deaminase, RNA-specific</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21.3</field>
+ <field name="info">
+Dyschromatosis symmetrica hereditaria [MIM:127400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADA">
+ <field name="name">ADA</field>
+ <field name="long_name">adenosine deaminase</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.11</field>
+ <field name="info">
+Severe combined immunodeficiency due to ADA deficiency [MIM:102700]
+Adenosine deaminase deficiency, partial [MIM:102700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADCY6">
+ <field name="name">ADCY6</field>
+ <field name="long_name">adenylate cyclase 6</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q12-q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADCY9">
+ <field name="name">ADCY9</field>
+ <field name="long_name">adenylate cyclase 9</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADD1">
+ <field name="name">ADD1</field>
+ <field name="long_name">adducin 1 (alpha)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.3</field>
+ <field name="info">
+Hypertension, essential, salt-sensitive [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADFN">
+ <field name="name">ADFN</field>
+ <field name="long_name">albinism-deafness syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26.3-q27.1</field>
+ <field name="info">
+Albinism-deafness syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADH1B">
+ <field name="name">ADH1B</field>
+ <field name="long_name">alcohol dehydrogenase 1B (class I), beta polypeptide</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q22</field>
+ <field name="info">
+Alcoholism, susceptibility to [MIM:103780]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADH1C">
+ <field name="name">ADH1C</field>
+ <field name="long_name">alcohol dehydrogenase 1C (class I), gamma polypeptide</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q22</field>
+ <field name="info">
+Parkinson disease, susceptibility to [MIM:168600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADH4">
+ <field name="name">ADH4</field>
+ <field name="long_name">alcohol dehydrogenase 4 (class II), pi polypeptide</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADH5">
+ <field name="name">ADH5</field>
+ <field name="long_name">alcohol dehydrogenase 5 (class III), chi polypeptide</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21-q25</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADHD1">
+ <field name="name">ADHD1</field>
+ <field name="long_name">Attention deficit-hyperactivity disorder, susceptibility to, 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13</field>
+ <field name="info">
+Attention deficit-hyperactivity disorder [MIM:143465]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADHD2">
+ <field name="name">ADHD2</field>
+ <field name="long_name">Attention deficit-hyperactivity disorder, susceptibility to, 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11</field>
+ <field name="info">
+Attention deficit-hyperactivity disorder [MIM:143465]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADHD3">
+ <field name="name">ADHD3</field>
+ <field name="long_name">Attention deficit-hyperactivity disorder, susceptibility to, 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q12</field>
+ <field name="info">
+Attention deficit-hyperactivity disorder [MIM:143465]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADHD4">
+ <field name="name">ADHD4</field>
+ <field name="long_name">Attention deficit-hyperactivity disorder, susceptibility to, 4</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13</field>
+ <field name="info">
+Attention deficit-hyperactivity disorder [MIM:143465]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADHD5">
+ <field name="name">ADHD5</field>
+ <field name="long_name">Attention deficit-hyperactivity disorder, susceptibility to, 5</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q21.1</field>
+ <field name="info">
+Attention deficit-hyperactivity disorder, susceptibility to, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADHD6">
+ <field name="name">ADHD6</field>
+ <field name="long_name">Attention deficit-hyperactivity disorder, susceptibility to, 6</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12.11</field>
+ <field name="info">
+Attention deficit-hyperactivity disorder, susceptibility to, 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADIPOQ">
+ <field name="name">ADIPOQ</field>
+ <field name="long_name">adiponectin, C1Q and collagen domain containing</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27</field>
+ <field name="info">
+Adiponectin deficiency [MIM:612556]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADIPOR1">
+ <field name="name">ADIPOR1</field>
+ <field name="long_name">adiponectin receptor 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.13-q41</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADIPQTL4">
+ <field name="name">ADIPQTL4</field>
+ <field name="long_name">Adiponectin, serum level of, QTL4</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23-q24</field>
+ <field name="info">
+Adiponectin, serum level of, QTL4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADM">
+ <field name="name">ADM</field>
+ <field name="long_name">adrenomedullin</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADORA1">
+ <field name="name">ADORA1</field>
+ <field name="long_name">adenosine A1 receptor</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADORA2A">
+ <field name="name">ADORA2A</field>
+ <field name="long_name">adenosine A2a receptor</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADORA3">
+ <field name="name">ADORA3</field>
+ <field name="long_name">adenosine A3 receptor</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p21-p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADRA1A">
+ <field name="name">ADRA1A</field>
+ <field name="long_name">adrenergic, alpha-1A-, receptor</field>
+ <field name="chromosome">20</field>
+ <field name="location">20</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADRA2A">
+ <field name="name">ADRA2A</field>
+ <field name="long_name">adrenergic, alpha-2A-, receptor</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24-q26</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADRA2B">
+ <field name="name">ADRA2B</field>
+ <field name="long_name">adrenergic, alpha-2B-, receptor</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADRA2C">
+ <field name="name">ADRA2C</field>
+ <field name="long_name">adrenergic, alpha-2C-, receptor</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.1</field>
+ <field name="info">
+Congestive heart failure and beta-blocker response, modifier of</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADRB1">
+ <field name="name">ADRB1</field>
+ <field name="long_name">adrenergic, beta-1-, receptor</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24-q26</field>
+ <field name="info">
+Resting heart rate [MIM:607276]
+Congestive heart failure and beta-blocker response, modifier of (3) 19</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADRB2">
+ <field name="name">ADRB2</field>
+ <field name="long_name">adrenergic, beta-2-, receptor, surface</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q32-q34</field>
+ <field name="info">
+Asthma, nocturnal, susceptibility to [MIM:600807]
+Obesity, susceptibility to [MIM:601665]
+Beta-2-adrenoreceptor agonist, reduced response to (3) 18</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADRB3">
+ <field name="name">ADRB3</field>
+ <field name="long_name">adrenergic, beta-3-, receptor</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p12-p11.2</field>
+ <field name="info">
+Obesity, susceptibility to [MIM:601665]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADRBK2">
+ <field name="name">ADRBK2</field>
+ <field name="long_name">adrenergic, beta, receptor kinase 2</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADSD">
+ <field name="name">ADSD</field>
+ <field name="long_name">Striatal degeneration, autosomal dominant</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13.3-q14.1</field>
+ <field name="info">
+Striatal degeneration, autosomal dominant</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ADSL">
+ <field name="name">ADSL</field>
+ <field name="long_name">adenylosuccinate lyase</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.1</field>
+ <field name="info">
+Adenylosuccinase deficiency [MIM:103050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AFA1">
+ <field name="name">AFA1</field>
+ <field name="long_name">Alopecia, androgenetic</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26</field>
+ <field name="info">
+Alopecia, androgenetic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AFD1">
+ <field name="name">AFD1</field>
+ <field name="long_name">acrofacial dysostosis 1, Nager type</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q32</field>
+ <field name="info">
+Acrofacial dysostosis, Nager type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AFP">
+ <field name="name">AFP</field>
+ <field name="long_name">alpha-fetoprotein</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q11-q13</field>
+ <field name="info">
+AFP deficiency, congenital
+Hereditary persistence of alpha-fetoprotein</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGA2">
+ <field name="name">AGA2</field>
+ <field name="long_name">Alopecia, androgenetic, 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq11-q12</field>
+ <field name="info">
+Alopecia, androgenetic, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGA3">
+ <field name="name">AGA3</field>
+ <field name="long_name">Alopecia, androgenetic, 3</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p11.22</field>
+ <field name="info">
+Alopecia, androgenetic, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGA">
+ <field name="name">AGA</field>
+ <field name="long_name">aspartylglucosaminidase</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q32-q33</field>
+ <field name="info">
+Aspartylglucosaminuria</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGER">
+ <field name="name">AGER</field>
+ <field name="long_name">advanced glycosylation end product-specific receptor</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGGF1">
+ <field name="name">AGGF1</field>
+ <field name="long_name">angiogenic factor with G patch and FHA domains 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGL">
+ <field name="name">AGL</field>
+ <field name="long_name">amylo-1, 6-glucosidase, 4-alpha-glucanotransferase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p21</field>
+ <field name="info">
+Glycogen storage disease IIIa [MIM:232400]
+Glycogen storage disease IIIb [MIM:232400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGMX2">
+ <field name="name">AGMX2</field>
+ <field name="long_name">agammaglobulinemia, X-linked 2 (with growth hormone deficiency)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22</field>
+ <field name="info">
+Agammaglobulinemia, type 2, X-linked</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGPAT2">
+ <field name="name">AGPAT2</field>
+ <field name="long_name">1-acylglycerol-3-phosphate O-acyltransferase 2 (lysophosphatidic acid acyltransferase, beta)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.3</field>
+ <field name="info">
+Lipodystrophy, congenital generalized, type 1 [MIM:608594]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGPS">
+ <field name="name">AGPS</field>
+ <field name="long_name">alkylglycerone phosphate synthase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31</field>
+ <field name="info">
+Rhizomelic chondrodysplasia punctata, type 3 [MIM:600121]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGRP">
+ <field name="name">AGRP</field>
+ <field name="long_name">agouti related protein homolog (mouse)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22</field>
+ <field name="info">
+Obesity, late-onset [MIM:601665]
+Leanness, inherited</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGSPX">
+ <field name="name">AGSPX</field>
+ <field name="long_name">Angio serpiginosum</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.3-q12</field>
+ <field name="info">
+Angio serpiginosum</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGTR1">
+ <field name="name">AGTR1</field>
+ <field name="long_name">angiotensin II receptor, type 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21-q25</field>
+ <field name="info">
+Hypertension, essential [MIM:145500]
+Renal tubular dysgenesis [MIM:267430]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGTR2">
+ <field name="name">AGTR2</field>
+ <field name="long_name">angiotensin II receptor, type 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22-q23</field>
+ <field name="info">
+Mental retardation, X-linked-88</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGT">
+ <field name="name">AGT</field>
+ <field name="long_name">angiotensinogen (serpin peptidase inhibitor, clade A, member 8)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42-q43</field>
+ <field name="info">
+Hypertension, essential, susceptibility to [MIM:145500]
+Preeclampsia, susceptibility to
+Renal tubular dysgenesis [MIM:267430]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AGXT">
+ <field name="name">AGXT</field>
+ <field name="long_name">alanine-glyoxylate aminotransferase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q36-q37</field>
+ <field name="info">
+Hyperoxaluria, primary, type 1 [MIM:259900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AHCY">
+ <field name="name">AHCY</field>
+ <field name="long_name">S-adenosylhomocysteine hydrolase</field>
+ <field name="chromosome">20</field>
+ <field name="location">20cen-q13.1</field>
+ <field name="info">
+Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AHI1">
+ <field name="name">AHI1</field>
+ <field name="long_name">Abelson helper integration site 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23.3</field>
+ <field name="info">
+Joubert syndrome-3 [MIM:608629]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AHRR">
+ <field name="name">AHRR</field>
+ <field name="long_name">aryl-hydrocarbon receptor repressor</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AHR">
+ <field name="name">AHR</field>
+ <field name="long_name">aryl hydrocarbon receptor</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AHSG">
+ <field name="name">AHSG</field>
+ <field name="long_name">alpha-2-HS-glycoprotein</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AICDA">
+ <field name="name">AICDA</field>
+ <field name="long_name">activation-induced cytidine deaminase</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+Immunodeficiency with hyper-IgM, type 2 [MIM:605258]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AIC">
+ <field name="name">AIC</field>
+ <field name="long_name">Aicardi syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22</field>
+ <field name="info">
+Aicardi syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AIED">
+ <field name="name">AIED</field>
+ <field name="long_name">Aland island eye disease (Forsius-Eriksson ocular albinism, ocular albinism type 2)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23</field>
+ <field name="info">
+Night blindness, congenital stationary, X-linked, type 2A [MIM:300071]
+Cone-rod dystrophy, X-linked, 3 [MIM:300476]
+Aland Island eye disease [MIM:300600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AIH3">
+ <field name="name">AIH3</field>
+ <field name="long_name">amelogenesis imperfecta 3, hypomaturation or hypoplastic type</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22-q28</field>
+ <field name="info">
+Amelogenesis imperfecta-3, hypoplastic type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AIPL1">
+ <field name="name">AIPL1</field>
+ <field name="long_name">aryl hydrocarbon receptor interacting protein-like 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.1</field>
+ <field name="info">
+Leber congenital amaurosis 4 [MIM:604393]
+Retinitis pigmentosa, juvenile
+Cone-rod dystrophy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AIP">
+ <field name="name">AIP</field>
+ <field name="long_name">aryl hydrocarbon receptor interacting protein</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.3</field>
+ <field name="info">
+Pituitary adenoma, growth hormone-secreting [MIM:102200]
+Pituitary adenoma, prolactin-secreting [MIM:600634]
+Pituitary adenoma, ACTH-secreting [MIM:219090]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AIRE">
+ <field name="name">AIRE</field>
+ <field name="long_name">autoimmune regulator</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia [MIM:240300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AIR">
+ <field name="name">AIR</field>
+ <field name="long_name">Acute insulin response (2)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+Acute insulin response</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AIS1">
+ <field name="name">AIS1</field>
+ <field name="long_name">autoimmune susceptibility 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+Autoimmune disease, susceptibility to, 1 [MIM:607836]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AIS2">
+ <field name="name">AIS2</field>
+ <field name="long_name">autoimmune susceptibility 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7</field>
+ <field name="info">
+Autoimmune disease, susceptibility to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AIS3">
+ <field name="name">AIS3</field>
+ <field name="long_name">autoimmune susceptibility 3 (vitiligo specific)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8</field>
+ <field name="info">
+Autoimmune disease, susceptibility to, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AIS4">
+ <field name="name">AIS4</field>
+ <field name="long_name">autoimmune disease, susceptibility to, 4</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q13-q21</field>
+ <field name="info">
+Autoimmune disease, susceptibility to, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AIS">
+ <field name="name">AIS</field>
+ <field name="long_name">Adolescent idiopathic scoliosis</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Scoliosis, idiopathic 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AITD1">
+ <field name="name">AITD1</field>
+ <field name="long_name">Autoimmune thyroid disease, susceptibility to, 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p11</field>
+ <field name="info">
+Autoimmune thyroid disease, susceptibility to, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AITD2">
+ <field name="name">AITD2</field>
+ <field name="long_name">Autoimmune thyroid disease, susceptibility to, 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31-q33</field>
+ <field name="info">
+Autoimmune thyroid disease, susceptibility to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AITD4">
+ <field name="name">AITD4</field>
+ <field name="long_name">Autoimmune thyroid disease, susceptibility to, 4</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q</field>
+ <field name="info">
+Autoimmune thyroid disease, susceptibility to, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AK1">
+ <field name="name">AK1</field>
+ <field name="long_name">adenylate kinase 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.1</field>
+ <field name="info">
+Hemolytic anemia due to adenylate kinase deficiency [MIM:612631]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AK2">
+ <field name="name">AK2</field>
+ <field name="long_name">adenylate kinase 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AKAP10">
+ <field name="name">AKAP10</field>
+ <field name="long_name">A kinase (PRKA) anchor protein 10</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.1</field>
+ <field name="info">
+Cardiac conduction defect, susceptibility to [MIM:115080]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AKAP13">
+ <field name="name">AKAP13</field>
+ <field name="long_name">A kinase (PRKA) anchor protein 13</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q24-q25</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AKAP2">
+ <field name="name">AKAP2</field>
+ <field name="long_name">A kinase (PRKA) anchor protein 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q31-q33</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AKAP9">
+ <field name="name">AKAP9</field>
+ <field name="long_name">A kinase (PRKA) anchor protein (yotiao) 9</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21-q22</field>
+ <field name="info">
+Long QT syndrome-11 [MIM:611820]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AKR1B1">
+ <field name="name">AKR1B1</field>
+ <field name="long_name">aldo-keto reductase family 1, member B1 (aldose reductase)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q35</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AKR1C2">
+ <field name="name">AKR1C2</field>
+ <field name="long_name">aldo-keto reductase family 1, member C2 (dihydrodiol dehydrogenase 2; bile acid binding protein; 3-alpha hydroxysteroid dehydrogenase, type III)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p15-p14</field>
+ <field name="info">
+Obesity, hyperphagia, and developmental delay</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AKR1C3">
+ <field name="name">AKR1C3</field>
+ <field name="long_name">aldo-keto reductase family 1, member C3 (3-alpha hydroxysteroid dehydrogenase, type II)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p15-p14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AKR1C4">
+ <field name="name">AKR1C4</field>
+ <field name="long_name">aldo-keto reductase family 1, member C4 (chlordecone reductase; 3-alpha hydroxysteroid dehydrogenase, type I; dihydrodiol dehydrogenase 4)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p15-p14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AKR1D1">
+ <field name="name">AKR1D1</field>
+ <field name="long_name">aldo-keto reductase family 1, member D1 (delta 4-3-ketosteroid-5-beta-reductase)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q32-q33</field>
+ <field name="info">
+Bile acid synthesis defect, congenital, 2 [MIM:235555]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AKT1">
+ <field name="name">AKT1</field>
+ <field name="long_name">v-akt murine thymoma viral oncogene homolog 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.3</field>
+ <field name="info">
+Breast cancer, somatic [MIM:114480]
+Colorectal cancer, somatic [MIM:114500]
+Ovarian cancer, somatic [MIM:604370]
+Schizophrenia, susceptibility to [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AKT2">
+ <field name="name">AKT2</field>
+ <field name="long_name">v-akt murine thymoma viral oncogene homolog 2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1-q13.2</field>
+ <field name="info">
+Diabetes mellitus, type II [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALAD">
+ <field name="name">ALAD</field>
+ <field name="long_name">aminolevulinate, delta-, dehydratase</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+Porphyria, acute hepatic [MIM:612740]
+Lead poisoning, susceptibility to [MIM:612740]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALAS2">
+ <field name="name">ALAS2</field>
+ <field name="long_name">aminolevulinate, delta-, synthase 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.21</field>
+ <field name="info">
+Anemia, sideroblastic, X-linked [MIM:300751]
+Protoporphyria, erythropoietic, X-linked dominant [MIM:300752]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALB">
+ <field name="name">ALB</field>
+ <field name="long_name">albumin</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q11-q13</field>
+ <field name="info">
+Analbuminemia
+Dysalbuminemic hyperthyroxinemia
+Dysalbuminemic hyperzincemia [MIM:194470]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALDH1A1">
+ <field name="name">ALDH1A1</field>
+ <field name="long_name">aldehyde dehydrogenase 1 family, member A1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALDH2">
+ <field name="name">ALDH2</field>
+ <field name="long_name">aldehyde dehydrogenase 2 family (mitochondrial)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.2</field>
+ <field name="info">
+Alcohol sensitivity, acute [MIM:610251]
+Hangover, susceptibility to [MIM:610251]
+Sublingual nitroglycerin, susceptibility to poor response to (3) 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALDH3A2">
+ <field name="name">ALDH3A2</field>
+ <field name="long_name">aldehyde dehydrogenase 3 family, member A2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+Sjogren-Larsson syndrome [MIM:270200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALDH4A1">
+ <field name="name">ALDH4A1</field>
+ <field name="long_name">aldehyde dehydrogenase 4 family, member A1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Hyperprolinemia, type II [MIM:239510]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALDH5A1">
+ <field name="name">ALDH5A1</field>
+ <field name="long_name">aldehyde dehydrogenase 5 family, member A1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p22</field>
+ <field name="info">
+Succinic semialdehyde dehydrogenase deficiency [MIM:271980]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALDH6A1">
+ <field name="name">ALDH6A1</field>
+ <field name="long_name">aldehyde dehydrogenase 6 family, member A1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3</field>
+ <field name="info">
+Methylmalonate semialdehyde dehydrogenase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALDH7A1">
+ <field name="name">ALDH7A1</field>
+ <field name="long_name">aldehyde dehydrogenase 7 family, member A1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Epilepsy, pyridoxine-dependent [MIM:266100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALDOA">
+ <field name="name">ALDOA</field>
+ <field name="long_name">aldolase A, fructose-bisphosphate</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p11.2</field>
+ <field name="info">
+Aldolase A deficiency [MIM:611881]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALDOB">
+ <field name="name">ALDOB</field>
+ <field name="long_name">aldolase B, fructose-bisphosphate</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22.3</field>
+ <field name="info">
+Fructose intolerance [MIM:229600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALG10">
+ <field name="name">ALG10</field>
+ <field name="long_name">asparagine-linked glycosylation 10, alpha-1,2-glucosyltransferase homolog (S. pombe)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p11.1</field>
+ <field name="info">
+Acquired long QT syndrome, reduced susceptibility to [MIM:152427]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALG12">
+ <field name="name">ALG12</field>
+ <field name="long_name">asparagine-linked glycosylation 12, alpha-1,6-mannosyltransferase homolog (S. cerevisiae)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.33</field>
+ <field name="info">
+Congenital disorder of glycosylation, type Ig [MIM:607143]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALG1">
+ <field name="name">ALG1</field>
+ <field name="long_name">asparagine-linked glycosylation 1, beta-1,4-mannosyltransferase homolog (S. cerevisiae)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+Congenital disorder of glycosylation, type Ik [MIM:608540]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALG2">
+ <field name="name">ALG2</field>
+ <field name="long_name">asparagine-linked glycosylation 2, alpha-1,3-mannosyltransferase homolog (S. cerevisiae)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22</field>
+ <field name="info">
+Congenital disorder of glycosylation, type Ii [MIM:607906]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALG3">
+ <field name="name">ALG3</field>
+ <field name="long_name">asparagine-linked glycosylation 3, alpha-1,3- mannosyltransferase homolog (S. cerevisiae)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27</field>
+ <field name="info">
+Congenital disorder of glycosylation, type Id [MIM:601110]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALG6">
+ <field name="name">ALG6</field>
+ <field name="long_name">asparagine-linked glycosylation 6, alpha-1,3-glucosyltransferase homolog (S. cerevisiae)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p22.3</field>
+ <field name="info">
+Congenital disorder of glycosylation, type Ic [MIM:603147]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALG8">
+ <field name="name">ALG8</field>
+ <field name="long_name">asparagine-linked glycosylation 8, alpha-1,3-glucosyltransferase homolog (S. cerevisiae)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11pter-p15.5</field>
+ <field name="info">
+Congenital disorder of glycosylation, type Ih [MIM:608104]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALG9">
+ <field name="name">ALG9</field>
+ <field name="long_name">asparagine-linked glycosylation 9, alpha-1,2-mannosyltransferase homolog (S. cerevisiae)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Congenital disorder of glycosylation, type Il [MIM:608776]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALK">
+ <field name="name">ALK</field>
+ <field name="long_name">anaplastic lymphoma receptor tyrosine kinase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p23</field>
+ <field name="info">
+Neuroblastoma, susceptibility to [MIM:256700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALMS1">
+ <field name="name">ALMS1</field>
+ <field name="long_name">Alstrom syndrome 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p13</field>
+ <field name="info">
+Alstrom syndrome [MIM:203800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALOX12B">
+ <field name="name">ALOX12B</field>
+ <field name="long_name">arachidonate 12-lipoxygenase, 12R type</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.1</field>
+ <field name="info">
+Ichthyosiform erythroderma, congenital, nonbullous, 1 [MIM:242100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALOX12">
+ <field name="name">ALOX12</field>
+ <field name="long_name">arachidonate 12-lipoxygenase</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALOX15">
+ <field name="name">ALOX15</field>
+ <field name="long_name">arachidonate 15-lipoxygenase</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALOX5AP">
+ <field name="name">ALOX5AP</field>
+ <field name="long_name">arachidonate 5-lipoxygenase-activating protein</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12</field>
+ <field name="info">
+Stroke, susceptibility to [MIM:601367]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALOX5">
+ <field name="name">ALOX5</field>
+ <field name="long_name">arachidonate 5-lipoxygenase</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q11.2</field>
+ <field name="info">
+Atherosclerosis, susceptibility to
+Asthma, diminished response to antileukotriene treatment in [MIM:600807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALOXE3">
+ <field name="name">ALOXE3</field>
+ <field name="long_name">arachidonate lipoxygenase 3</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.1</field>
+ <field name="info">
+Ichthyosiform erythroderma, congenital, nonbullous, 1 [MIM:242100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALPL">
+ <field name="name">ALPL</field>
+ <field name="long_name">alkaline phosphatase, liver/bone/kidney</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.1-p34</field>
+ <field name="info">
+Hypophosphatasia, infantile [MIM:241500]
+Hypophosphatasia, childhood [MIM:241510]
+Odontohypophosphatasia [MIM:146300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALPQTL1">
+ <field name="name">ALPQTL1</field>
+ <field name="long_name">Alkaline phosphatase, plasma level of, QTL1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.13</field>
+ <field name="info">
+Alkaline phosphatase, plasma level of, QTL1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALPQTL2">
+ <field name="name">ALPQTL2</field>
+ <field name="long_name">Alkaline phosphatase, plasma level of, QTL 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Alkaline phosphatase, plasma level of, QTL 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALPQTL3">
+ <field name="name">ALPQTL3</field>
+ <field name="long_name">Alkaline phosphatase, plasma level of, QTL3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p22</field>
+ <field name="info">
+Alkaline phosphatase, plasma level of, QTL3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALPQTL4">
+ <field name="name">ALPQTL4</field>
+ <field name="long_name">Alkaline phosphatase, plasma level of, QTL4</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21</field>
+ <field name="info">
+Alkaline phosphatase, plasma level of, QTL4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALRH">
+ <field name="name">ALRH</field>
+ <field name="long_name">Allergic rhinitis</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Asthma, susceptibility to [MIM:600807]
+Allergic rhinitis, susceptibility to [MIM:607154]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALS2">
+ <field name="name">ALS2</field>
+ <field name="long_name">amyotrophic lateral sclerosis 2 (juvenile)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33</field>
+ <field name="info">
+Amyotrophic lateral sclerosis, juvenile [MIM:205100]
+Primary lateral sclerosis, juvenile [MIM:606353]
+Spastic paralysis, infantile onset ascending [MIM:607225]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALS3">
+ <field name="name">ALS3</field>
+ <field name="long_name">amyotrophic lateral sclerosis 3 (autosomal dominant)</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21</field>
+ <field name="info">
+Amyotrophic lateral sclerosis 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALS5">
+ <field name="name">ALS5</field>
+ <field name="long_name">amyotrophic lateral sclerosis 5</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15.1-q21.1</field>
+ <field name="info">
+Amyotrophic lateral sclerosis-5, juvenile recessive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALS6">
+ <field name="name">ALS6</field>
+ <field name="long_name">amyotrophic lateral sclerosis 6</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q12</field>
+ <field name="info">
+Amyotrophic lateral sclerosis 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALS7">
+ <field name="name">ALS7</field>
+ <field name="long_name">amyotrophic lateral sclerosis 7</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p13</field>
+ <field name="info">
+Amyotrophic lateral sclerosis 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ALX4">
+ <field name="name">ALX4</field>
+ <field name="long_name">ALX homeobox 4</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p11.2</field>
+ <field name="info">
+Parietal foramina 2 [MIM:609597]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMACR">
+ <field name="name">AMACR</field>
+ <field name="long_name">alpha-methylacyl-CoA racemase</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13.2-q11.1</field>
+ <field name="info">
+Alpha-methylacyl-CoA racemase deficiency
+Bile acid synthesis defect, congenital, 4 [MIM:214950]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMCBX2">
+ <field name="name">AMCBX2</field>
+ <field name="long_name">Atypical mycobacteriosis, familial, X-linked 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp21.2-q26.3</field>
+ <field name="info">
+Atypical mycobacteriosis, familial, X-linked 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMCD2B">
+ <field name="name">AMCD2B</field>
+ <field name="long_name">arthrogryposis multiplex congenita, distal, type 2B</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Arthyrgryposis, distal, type 2B [MIM:601680]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMCN">
+ <field name="name">AMCN</field>
+ <field name="long_name">arthrogryposis multiplex congenita, neurogenic</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q35</field>
+ <field name="info">
+Arthrogryposis multiplex congenita, neurogenic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMDM">
+ <field name="name">AMDM</field>
+ <field name="long_name">acromesomelic dysplasia, Maroteaux type</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21-p12</field>
+ <field name="info">
+Acromesomelic dysplasia, Maroteaux type [MIM:602875]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMELX">
+ <field name="name">AMELX</field>
+ <field name="long_name">amelogenin (amelogenesis imperfecta 1, X-linked)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3-p22.1</field>
+ <field name="info">
+Amelogenesis imperfecta, hypoplastic/hypomaturation type [MIM:301200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMELY">
+ <field name="name">AMELY</field>
+ <field name="long_name">amelogenin, Y-linked</field>
+ <field name="chromosome">Y</field>
+ <field name="location">Yp11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMHR2">
+ <field name="name">AMHR2</field>
+ <field name="long_name">anti-Mullerian hormone receptor, type II</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Persistent Mullerian duct syndrome, type II [MIM:261550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMH">
+ <field name="name">AMH</field>
+ <field name="long_name">anti-Mullerian hormone</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3-p13.2</field>
+ <field name="info">
+Persistent Mullerian duct syndrome, type I [MIM:261550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMLCR2">
+ <field name="name">AMLCR2</field>
+ <field name="long_name">acute myeloid leukemia chromosome region 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22</field>
+ <field name="info">
+Leukemia, acute myelogenous [MIM:601626]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMMECR1">
+ <field name="name">AMMECR1</field>
+ <field name="long_name">Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22.3</field>
+ <field name="info">
+Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis [MIM:300194]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMN">
+ <field name="name">AMN</field>
+ <field name="long_name">amnionless homolog (mouse)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32</field>
+ <field name="info">
+Megaloblastic anemia-1, Norwegian type [MIM:261100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMPD1">
+ <field name="name">AMPD1</field>
+ <field name="long_name">adenosine monophosphate deaminase 1 (isoform M)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p21-p13</field>
+ <field name="info">
+Myoadenylate deaminase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMPD3">
+ <field name="name">AMPD3</field>
+ <field name="long_name">adenosine monophosphate deaminase (isoform E)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11pter-p13</field>
+ <field name="info">
+AMP deaminase deficiency, erythrocytic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AMT">
+ <field name="name">AMT</field>
+ <field name="long_name">aminomethyltransferase</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.2-p21.1</field>
+ <field name="info">
+Glycine encephalopathy [MIM:605899]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANBC">
+ <field name="name">ANBC</field>
+ <field name="long_name">Aneurysmal bone cysts</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22</field>
+ <field name="info">
+Aneurysmal bone cysts</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANCR">
+ <field name="name">ANCR</field>
+ <field name="long_name">Angelman syndrome chromosome region</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q11-q13</field>
+ <field name="info">
+Angelman syndrome [MIM:105830]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANC">
+ <field name="name">ANC</field>
+ <field name="long_name">Anal canal carcinoma</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22-qter</field>
+ <field name="info">
+Anal canal carcinoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANE1">
+ <field name="name">ANE1</field>
+ <field name="long_name">acute necrotizing encephalopathy 1 (autosomal dominant)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q11-q13</field>
+ <field name="info">
+Encephalopathy, acute necrotizing 1 [MIM:608033]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANGPTL3">
+ <field name="name">ANGPTL3</field>
+ <field name="long_name">angiopoietin-like 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANGPTL4">
+ <field name="name">ANGPTL4</field>
+ <field name="long_name">angiopoietin-like 4</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Reduced triglycerides, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANGPTL5">
+ <field name="name">ANGPTL5</field>
+ <field name="long_name">angiopoietin-like 5</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANG">
+ <field name="name">ANG</field>
+ <field name="long_name">angiogenin, ribonuclease, RNase A family, 5</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2</field>
+ <field name="info">
+Amyotrophic lateral sclerosis 9 [MIM:611895]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANIB10">
+ <field name="name">ANIB10</field>
+ <field name="long_name">Aneurysm, intracranial berry, 10</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q12.1</field>
+ <field name="info">
+Aneurysm, intracranial berry, 10</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANIB1">
+ <field name="name">ANIB1</field>
+ <field name="long_name">aneurysm, intracranial berry 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.2</field>
+ <field name="info">
+Aneurysm, intracranial berry, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANIB2">
+ <field name="name">ANIB2</field>
+ <field name="long_name">aneurysm, intracranial berry 2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+Aneurysm, intracranial berry, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANIB3">
+ <field name="name">ANIB3</field>
+ <field name="long_name">aneurysm, intracranial berry 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.13-p34.3</field>
+ <field name="info">
+Aneurysm, intracranial berry, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANIB4">
+ <field name="name">ANIB4</field>
+ <field name="long_name">aneurysm, intracranial berry 4</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.2-p14.3</field>
+ <field name="info">
+Aneurysm, intracranial berry, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANIB5">
+ <field name="name">ANIB5</field>
+ <field name="long_name">Aneurysm, intracranial berry, 5</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p15-q14</field>
+ <field name="info">
+Aneurysm, intracranial berry, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANIB6">
+ <field name="name">ANIB6</field>
+ <field name="long_name">Aneurysm, intracranial berry, 6</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21</field>
+ <field name="info">
+Aneurysm, intracranial berry, 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANIB7">
+ <field name="name">ANIB7</field>
+ <field name="long_name">Aneurysm, intracranial berry, 7</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q24-q25</field>
+ <field name="info">
+Aneurysm, intracranial berry, 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANIB8">
+ <field name="name">ANIB8</field>
+ <field name="long_name">Aneurysm, intracranial berry, 8</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q23</field>
+ <field name="info">
+Aneurysm, intracranial berry, 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANIB9">
+ <field name="name">ANIB9</field>
+ <field name="long_name">Aneurysm, intracranial berry, 9</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33.1</field>
+ <field name="info">
+Aneurysm, intracranial berry, 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANIC">
+ <field name="name">ANIC</field>
+ <field name="long_name">Anosmia, isolated congenital</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.23-q12.2</field>
+ <field name="info">
+Anosmia, isolated congenital</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANK1">
+ <field name="name">ANK1</field>
+ <field name="long_name">ankyrin 1, erythrocytic</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p11.2</field>
+ <field name="info">
+Spherocytosis, type 1 [MIM:182900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANK2">
+ <field name="name">ANK2</field>
+ <field name="long_name">ankyrin 2, neuronal</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q25-q27</field>
+ <field name="info">
+Long QT syndrome-4 [MIM:600919]
+Cardiac arrhythmia, ankyrin-B-related [MIM:600919]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANKH">
+ <field name="name">ANKH</field>
+ <field name="long_name">ankylosis, progressive homolog (mouse)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.2-p14.1</field>
+ <field name="info">
+Craniometaphyseal dysplasia [MIM:123000]
+Chondrocalcinosis 2 [MIM:118600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANKK1">
+ <field name="name">ANKK1</field>
+ <field name="long_name">ankyrin repeat and kinase domain containing 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.2</field>
+ <field name="info">
+Dopamine receptor D2, reduced brain density of</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANMA">
+ <field name="name">ANMA</field>
+ <field name="long_name">Anisomastia</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q13-q21</field>
+ <field name="info">
+Anisomastia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANON">
+ <field name="name">ANON</field>
+ <field name="long_name">Anorexia nervosa, susceptibility to</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p</field>
+ <field name="info">
+Anorexia nervosa, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANOP1">
+ <field name="name">ANOP1</field>
+ <field name="long_name">anophthalmos 1 (with mental retardation, without limb anomalies or dental or urogenital abnormalities)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq27-q28</field>
+ <field name="info">
+Microphthalmia, syndromic 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANTXR1">
+ <field name="name">ANTXR1</field>
+ <field name="long_name">anthrax toxin receptor 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p13.1</field>
+ <field name="info">
+Hemangioma, capillary infantile, susceptibility to [MIM:602089]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANTXR2">
+ <field name="name">ANTXR2</field>
+ <field name="long_name">anthrax toxin receptor 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21</field>
+ <field name="info">
+Fibromatosis, juvenile hyaline [MIM:228600]
+Hyalinosis, infantile systemic [MIM:236490]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANXA11">
+ <field name="name">ANXA11</field>
+ <field name="long_name">annexin A11</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.3-q23.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ANXA5">
+ <field name="name">ANXA5</field>
+ <field name="long_name">annexin A5</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q26-q28</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AOAH">
+ <field name="name">AOAH</field>
+ <field name="long_name">acyloxyacyl hydrolase (neutrophil)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AOCH">
+ <field name="name">AOCH</field>
+ <field name="long_name">Acromegaloid features, overgrowth, cleft palate, and hernia</field>
+ <field name="chromosome">11</field>
+ <field name="location">11</field>
+ <field name="info">
+Acromegaloid features, overgrowth, cleft palate, and hernia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AOMS1">
+ <field name="name">AOMS1</field>
+ <field name="long_name">Abdominal obesity-metabolic syndrome QTL1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27</field>
+ <field name="info">
+Abdominal obesity-metabolic syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AOMS2">
+ <field name="name">AOMS2</field>
+ <field name="long_name">abdominal obesity-metabolic syndrome QTL2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p12</field>
+ <field name="info">
+Abdominal obesity-metabolic syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AP1S2">
+ <field name="name">AP1S2</field>
+ <field name="long_name">adaptor-related protein complex 1, sigma 2 subunit</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22</field>
+ <field name="info">
+Mental retardation, X-linked 59 [MIM:300630]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AP3B1">
+ <field name="name">AP3B1</field>
+ <field name="long_name">adaptor-related protein complex 3, beta 1 subunit</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q14.1</field>
+ <field name="info">
+Hermansky-Pudlak syndrome 2 [MIM:608233]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APAF1">
+ <field name="name">APAF1</field>
+ <field name="long_name">apoptotic peptidase activating factor 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="APBA2">
+ <field name="name">APBA2</field>
+ <field name="long_name">amyloid beta (A4) precursor protein-binding, family A, member 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="APBB1">
+ <field name="name">APBB1</field>
+ <field name="long_name">amyloid beta (A4) precursor protein-binding, family B, member 1 (Fe65)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="APBB2">
+ <field name="name">APBB2</field>
+ <field name="long_name">amyloid beta (A4) precursor protein-binding, family B, member 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p14</field>
+ <field name="info">
+Alzheimer disease, late-onset [MIM:104300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APCS">
+ <field name="name">APCS</field>
+ <field name="long_name">amyloid P component, serum</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21-q23</field>
+ <field name="info">
+Amyloidosis, secondary, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APC">
+ <field name="name">APC</field>
+ <field name="long_name">adenomatous polyposis coli</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q21-q22</field>
+ <field name="info">
+Adenomatous polyposis coli [MIM:175100]
+Gastric cancer, somatic [MIM:137215]
+Adenoma, periampullary
+Hepatoblastoma
+Desmoid disease, hereditary [MIM:135290]
+Gardner syndrome
+Brain tumor-polyposis syndrome 2
+Colorectal cancer, somatic [MIM:114500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APH1B">
+ <field name="name">APH1B</field>
+ <field name="long_name">anterior pharynx defective 1 homolog B (C. elegans)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="APMR2">
+ <field name="name">APMR2</field>
+ <field name="long_name">Alopecia with mental retardation syndrome 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.2-q26.31</field>
+ <field name="info">
+Alopecia with mental retardation syndrome 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOA1">
+ <field name="name">APOA1</field>
+ <field name="long_name">apolipoprotein A-I</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+ApoA-I and apoC-III deficiency, combined
+Hypoalphalipoproteinemia [MIM:604091]
+Corneal clouding, autosomal recessive
+Amyloidosis, 3 or more types [MIM:105200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOA2">
+ <field name="name">APOA2</field>
+ <field name="long_name">apolipoprotein A-II</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21-q23</field>
+ <field name="info">
+Apolipoprotein A-II deficiency
+Hypercholesterolemia, familial, modification of [MIM:143890]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOA4">
+ <field name="name">APOA4</field>
+ <field name="long_name">apolipoprotein A-IV</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOA5">
+ <field name="name">APOA5</field>
+ <field name="long_name">apolipoprotein A-V</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Hypertriglyceridemia, susceptibility to [MIM:145750]
+Hyperchylomicronemia, late-onset [MIM:144650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOBEC3B">
+ <field name="name">APOBEC3B</field>
+ <field name="long_name">apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3B</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOB">
+ <field name="name">APOB</field>
+ <field name="long_name">apolipoprotein B (including Ag(x) antigen)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p24</field>
+ <field name="info">
+Hypobetalipoproteinemia
+Hypobetalipoproteinemia, normotriglyceridemic
+Hypercholesterolemia, due to ligand-defective apo B [MIM:144010]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOC1">
+ <field name="name">APOC1</field>
+ <field name="long_name">apolipoprotein C-I</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOC2">
+ <field name="name">APOC2</field>
+ <field name="long_name">apolipoprotein C-II</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+Hyperlipoproteinemia, type Ib [MIM:207750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOC3">
+ <field name="name">APOC3</field>
+ <field name="long_name">apolipoprotein C-III</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Apolipoprotein C3 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOC4">
+ <field name="name">APOC4</field>
+ <field name="long_name">apolipoprotein C-IV</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOD">
+ <field name="name">APOD</field>
+ <field name="long_name">apolipoprotein D</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.2-qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOE">
+ <field name="name">APOE</field>
+ <field name="long_name">apolipoprotein E</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+Hyperlipoproteinemia, type III
+Myocardial infarction susceptibility
+Sea-blue histiocyte disease [MIM:269600]
+Alzheimer disease-2 [MIM:104310]
+Macular degeneration, age-related [MIM:603075]
+Lipoprotein glomerulopathy [MIM:611771]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOH">
+ <field name="name">APOH</field>
+ <field name="long_name">apolipoprotein H (beta-2-glycoprotein I)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23-qter</field>
+ <field name="info">
+Apolipoprotein H deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOL1">
+ <field name="name">APOL1</field>
+ <field name="long_name">apolipoprotein L, 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.3</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOL2">
+ <field name="name">APOL2</field>
+ <field name="long_name">apolipoprotein L, 2</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.3</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APOL4">
+ <field name="name">APOL4</field>
+ <field name="long_name">apolipoprotein L, 4</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.3</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APP">
+ <field name="name">APP</field>
+ <field name="long_name">amyloid beta (A4) precursor protein</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q21</field>
+ <field name="info">
+Cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants [MIM:605714]
+Alzheimer disease 1, familial [MIM:104300]
+Dementia, early-onset progressive, autosomal recessive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APRT">
+ <field name="name">APRT</field>
+ <field name="long_name">adenine phosphoribosyltransferase</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.3</field>
+ <field name="info">
+Urolithiasis, 2,8-dihydroxyadenine</field>
+</record>
+<record model="gnuhealth.disease.gene" id="APTX">
+ <field name="name">APTX</field>
+ <field name="long_name">aprataxin</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p13.3</field>
+ <field name="info">
+Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia [MIM:208920]
+Coenzyme Q10 deficiency [MIM:607426]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AQP1">
+ <field name="name">AQP1</field>
+ <field name="long_name">aquaporin 1 (Colton blood group)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14</field>
+ <field name="info">
+Blood group, Colton [MIM:110450]
+Aquaporin-1 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AQP2">
+ <field name="name">AQP2</field>
+ <field name="long_name">aquaporin 2 (collecting duct)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Diabetes insipidus, nephrogenic [MIM:125800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AQP3">
+ <field name="name">AQP3</field>
+ <field name="long_name">aquaporin 3 (Gill blood group)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p13</field>
+ <field name="info">
+Blood group GIL [MIM:607457]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AQP4">
+ <field name="name">AQP4</field>
+ <field name="long_name">aquaporin 4</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q11.2-q12.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AQP5">
+ <field name="name">AQP5</field>
+ <field name="long_name">aquaporin 5</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AQP7">
+ <field name="name">AQP7</field>
+ <field name="long_name">aquaporin 7</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AQP9">
+ <field name="name">AQP9</field>
+ <field name="long_name">aquaporin 9</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22</field>
+ <field name="info">
+Glycerol release during exercise, defective</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARCC1">
+ <field name="name">ARCC1</field>
+ <field name="long_name">Age-related cortical cataract 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12-q12</field>
+ <field name="info">
+Cataract, age-related cortical, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARC">
+ <field name="name">ARC</field>
+ <field name="long_name">activity-regulated cytoskeleton-associated protein</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AREI">
+ <field name="name">AREI</field>
+ <field name="long_name">Exfoliative ichthyosis, autosomal recessive</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Exfoliative ichthyosis, autosomal recessive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARFGEF2">
+ <field name="name">ARFGEF2</field>
+ <field name="long_name">ADP-ribosylation factor guanine nucleotide-exchange factor 2 (brefeldin A-inhibited)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.13</field>
+ <field name="info">
+Periventricular heterotopia with microcephaly [MIM:608097]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARG1">
+ <field name="name">ARG1</field>
+ <field name="long_name">arginase, liver</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23</field>
+ <field name="info">
+Argininemia [MIM:207800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARHGAP26">
+ <field name="name">ARHGAP26</field>
+ <field name="long_name">Rho GTPase activating protein 26</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Leukemia, juvenile myelomonocytic [MIM:607785]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARHGEF10">
+ <field name="name">ARHGEF10</field>
+ <field name="long_name">Rho guanine nucleotide exchange factor (GEF) 10</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23</field>
+ <field name="info">
+Slowed nerve conduction velocity, AD [MIM:608236]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARHGEF12">
+ <field name="name">ARHGEF12</field>
+ <field name="long_name">Rho guanine nucleotide exchange factor (GEF) 12</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.3</field>
+ <field name="info">
+Leukemia, acute myeloid [MIM:601626]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARHGEF6">
+ <field name="name">ARHGEF6</field>
+ <field name="long_name">Rac/Cdc42 guanine nucleotide exchange factor (GEF) 6</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26</field>
+ <field name="info">
+Mental retardation, X-linked nonspecific, type 46 [MIM:300436]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARHGEF9">
+ <field name="name">ARHGEF9</field>
+ <field name="long_name">Cdc42 guanine nucleotide exchange factor (GEF) 9</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22.1</field>
+ <field name="info">
+Hyperekplexia and epilepsy [MIM:300607]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARHI1">
+ <field name="name">ARHI1</field>
+ <field name="long_name">Age-related hearing impairment 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.13-q24.22</field>
+ <field name="info">
+Age-related hearing impairment 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARL11">
+ <field name="name">ARL11</field>
+ <field name="long_name">ADP-ribosylation factor-like 11</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARL13B">
+ <field name="name">ARL13B</field>
+ <field name="long_name">ADP-ribosylation factor-like 13B</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q11.2</field>
+ <field name="info">
+Joubert syndrome [MIM:612291]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARL6">
+ <field name="name">ARL6</field>
+ <field name="long_name">ADP-ribosylation factor-like 6</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p12-q13</field>
+ <field name="info">
+Bardet-Biedl syndrome 3 [MIM:209900]
+Bardet-Biedl syndrome 1, modifier of [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARMET">
+ <field name="name">ARMET</field>
+ <field name="long_name">arginine-rich, mutated in early stage tumors</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.1</field>
+ <field name="info">
+Pancreatic cancer [MIM:260350]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARNT">
+ <field name="name">ARNT</field>
+ <field name="long_name">aryl hydrocarbon receptor nuclear translocator</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Leukemia, acute myeloblastic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARSA">
+ <field name="name">ARSA</field>
+ <field name="long_name">arylsulfatase A</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.31-qter</field>
+ <field name="info">
+Metachromatic leukodystrophy [MIM:250100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARSB">
+ <field name="name">ARSB</field>
+ <field name="long_name">arylsulfatase B</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q11-q13</field>
+ <field name="info">
+Maroteaux-Lamy syndrome, several forms [MIM:253200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARSE">
+ <field name="name">ARSE</field>
+ <field name="long_name">arylsulfatase E (chondrodysplasia punctata 1)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3</field>
+ <field name="info">
+Chondrodysplasia punctata, X-linked recessive [MIM:302950]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ART4">
+ <field name="name">ART4</field>
+ <field name="long_name">ADP-ribosyltransferase 4 (Dombrock blood group)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13-p12</field>
+ <field name="info">
+Blood group, Dombrock</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARVD1">
+ <field name="name">ARVD1</field>
+ <field name="long_name">arrhythmogenic right ventricular dysplasia 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q12-q22</field>
+ <field name="info">
+Arrhythmogenic right ventricular dysplasia-3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARVD3">
+ <field name="name">ARVD3</field>
+ <field name="long_name">arrhythmogenic right ventricular dysplasia 3</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q12-q22</field>
+ <field name="info">
+Arrhythmogenic right ventricular dysplasia-3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARVD4">
+ <field name="name">ARVD4</field>
+ <field name="long_name">arrhythmogenic right ventricular dysplasia 4</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q32.1-q32.3</field>
+ <field name="info">
+Arrhythmogenic right ventricular dysplasia-4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARVD5">
+ <field name="name">ARVD5</field>
+ <field name="long_name">arrhythmogenic right ventricular dysplasia 5</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25</field>
+ <field name="info">
+Arrhythmogenic right ventricular dysplasia, familial, 5 [MIM:604400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARVD6">
+ <field name="name">ARVD6</field>
+ <field name="long_name">arrhythmogenic right ventricular dysplasia 6</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p14-p12</field>
+ <field name="info">
+Arrhythmogenic right ventricular dysplasia-6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARVD7">
+ <field name="name">ARVD7</field>
+ <field name="long_name">Arrhythmogenic right ventricular dysplasia, familial, 7</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.3</field>
+ <field name="info">
+Arrhythmogenic right ventricular dysplasia-7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ARX">
+ <field name="name">ARX</field>
+ <field name="long_name">aristaless related homeobox</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.13</field>
+ <field name="info">
+Epilepsy, myoclonic, with mental retardation and spasticity [MIM:300432]
+Epileptic encephalopathy, early infantile, 1 [MIM:308350]
+Lissencephaly, X-linked 2 [MIM:300215]
+Mental retardation, X-linked 36/43/54 [MIM:300419]
+Proud syndrome [MIM:300004]
+Partington syndrome [MIM:309510]
+Hydranencephaly with abnormal genitalia [MIM:300215]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AR">
+ <field name="name">AR</field>
+ <field name="long_name">androgen receptor</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq11-q12</field>
+ <field name="info">
+Androgen insensitivity [MIM:300068]
+Spinal and bulbar muscular atrophy of Kennedy [MIM:313200]
+Androgen insensitivity, partial, with or without breast cancer [MIM:312300]
+Prostate cancer, susceptibility to [MIM:176807]
+Hypospadias 1, X-linked [MIM:300633]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AS3MT">
+ <field name="name">AS3MT</field>
+ <field name="long_name">arsenic (+3 oxidation state) methyltransferase</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASCL1">
+ <field name="name">ASCL1</field>
+ <field name="long_name">achaete-scute complex homolog 1 (Drosophila)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q22-q23</field>
+ <field name="info">
+Central hypoventilation syndrome, congenital [MIM:209880]
+Haddad syndrome [MIM:209880]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASD1">
+ <field name="name">ASD1</field>
+ <field name="long_name">atrial septal defect 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p</field>
+ <field name="info">
+Atrial septal defect, secundum type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASIP">
+ <field name="name">ASIP</field>
+ <field name="long_name">agouti signaling protein, nonagouti homolog (mouse)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11.2</field>
+ <field name="info">
+Skin/hair/eye pigmentation 9, dark/light hair [MIM:611742]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASL">
+ <field name="name">ASL</field>
+ <field name="long_name">argininosuccinate lyase</field>
+ <field name="chromosome">7</field>
+ <field name="location">7cen-q11.2</field>
+ <field name="info">
+Argininosuccinic aciduria [MIM:207900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASMD">
+ <field name="name">ASMD</field>
+ <field name="long_name">anterior segment mesenchymal dysgenesis</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+Anterior segment mesenchymal dysgenesis [MIM:107250]
+Aphakia, congenital primary [MIM:610256]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASMT">
+ <field name="name">ASMT</field>
+ <field name="long_name">acetylserotonin O-methyltransferase</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xpter-p22.32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASPA">
+ <field name="name">ASPA</field>
+ <field name="long_name">aspartoacylase (Canavan disease)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17pter-p13</field>
+ <field name="info">
+Canavan disease [MIM:271900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASPG1">
+ <field name="name">ASPG1</field>
+ <field name="long_name">Asperger syndrome, susceptibility to, 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q25-q27</field>
+ <field name="info">
+Asperger syndrome, susceptibility to, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASPG2">
+ <field name="name">ASPG2</field>
+ <field name="long_name">Asperger syndrome, susceptibility to, 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13</field>
+ <field name="info">
+Asperger syndrome, susceptibility to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASPG3">
+ <field name="name">ASPG3</field>
+ <field name="long_name">Asperger syndrome, susceptibility to, 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21-q22</field>
+ <field name="info">
+Asperger syndrome, susceptibility to, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASPG4">
+ <field name="name">ASPG4</field>
+ <field name="long_name">Asperger syndrome, susceptibility to, 4</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p24-p21</field>
+ <field name="info">
+Asperger syndrome, susceptibility to, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASPM">
+ <field name="name">ASPM</field>
+ <field name="long_name">asp (abnormal spindle) homolog, microcephaly associated (Drosophila)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31</field>
+ <field name="info">
+Microcephaly, primary autosomal recessive, 5, with or without simplified gyral pattern [MIM:608716]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASPN">
+ <field name="name">ASPN</field>
+ <field name="long_name">asporin</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q21.3-q22</field>
+ <field name="info">
+Osteoarthritis susceptibility 3 [MIM:607850]
+Lumbar disc degeneration [MIM:603932]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASPSCR1">
+ <field name="name">ASPSCR1</field>
+ <field name="long_name">alveolar soft part sarcoma chromosome region, candidate 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+Alveolar soft-part sarcoma [MIM:606243]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASRT3">
+ <field name="name">ASRT3</field>
+ <field name="long_name">Asthma-related traits, susceptibility to, 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p16</field>
+ <field name="info">
+Asthma-related traits, susceptibility to, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASRT4">
+ <field name="name">ASRT4</field>
+ <field name="long_name">Asthma-related traits, susceptibility to, 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+Asthma-related traits, susceptibility to, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASRT6">
+ <field name="name">ASRT6</field>
+ <field name="long_name">Asthma-related traits, susceptibility to, 6</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+Asthma-related traits, susceptibility to, 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ASSP2">
+ <field name="name">ASSP2</field>
+ <field name="long_name">argininosuccinate synthetase pseudogene 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.1</field>
+ <field name="info">
+Citrullinemia [MIM:215700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATCAY">
+ <field name="name">ATCAY</field>
+ <field name="long_name">ataxia, cerebellar, Cayman type</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Ataxia, cerebellar, Cayman type [MIM:601238]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATD">
+ <field name="name">ATD</field>
+ <field name="long_name">asphixiating thoracic dystrophy (chondroectodermal dysplasia-like syndrome)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q13</field>
+ <field name="info">
+Asphyxiating thoracic dystrophy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATF1">
+ <field name="name">ATF1</field>
+ <field name="long_name">activating transcription factor 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATF6">
+ <field name="name">ATF6</field>
+ <field name="long_name">activating transcription factor 6</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q22-q23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATFB1">
+ <field name="name">ATFB1</field>
+ <field name="long_name">Atrial fibrillation, familial 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22-q24</field>
+ <field name="info">
+Atrial fibrillation, familial, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATFB3">
+ <field name="name">ATFB3</field>
+ <field name="long_name">familial atrial fibrillation 3</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Long QT syndrome-1 [MIM:192500]
+Jervell and Lange-Nielsen syndrome [MIM:220400]
+Atrial fibrillation, familial, 3 [MIM:607554]
+Torsades de pointes, drug-associated
+Short QT syndrome-2 [MIM:609621]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATFB5">
+ <field name="name">ATFB5</field>
+ <field name="long_name">Atrial fibrillation, familial, 5</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q25</field>
+ <field name="info">
+Atrial fibrillation, familial, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATG16L1">
+ <field name="name">ATG16L1</field>
+ <field name="long_name">ATG16 autophagy related 16-like 1 (S. cerevisiae)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.1</field>
+ <field name="info">
+Inflammatory bowel disease 10, susceptibility to [MIM:611081]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATHS">
+ <field name="name">ATHS</field>
+ <field name="long_name">atherosclerosis susceptibility (lipoprotein associated)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3-p13.2</field>
+ <field name="info">
+Atherosclerosis, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATIC">
+ <field name="name">ATIC</field>
+ <field name="long_name">5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35</field>
+ <field name="info">
+AICA-ribosiduria due to ATIC deficiency [MIM:608688]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATM">
+ <field name="name">ATM</field>
+ <field name="long_name">ataxia telangiectasia mutated</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22.3</field>
+ <field name="info">
+Ataxia-telangiectasia [MIM:208900]
+Lymphoma, B-cell non-Hodgkin, somatic
+Breast cancer, susceptibility to [MIM:114480]
+Lymphoma, mantle cell
+T-cell prolymphocytic leukemia, sporadic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATN1">
+ <field name="name">ATN1</field>
+ <field name="long_name">atrophin 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.31</field>
+ <field name="info">
+Dentatorubro-pallidoluysian atrophy [MIM:125370]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATOD3">
+ <field name="name">ATOD3</field>
+ <field name="long_name">Dermatitis, atopic, 3</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p</field>
+ <field name="info">
+Dermatitis, atopic [MIM:603165]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATOD5">
+ <field name="name">ATOD5</field>
+ <field name="long_name">Dermatitis, atopic, 5</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12-q14</field>
+ <field name="info">
+Dermatitis, atopic [MIM:603165]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATOD6">
+ <field name="name">ATOD6</field>
+ <field name="long_name">Dermatitis, atopic, 6</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31-q33</field>
+ <field name="info">
+Dermatitis, atopic [MIM:603165]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP10A">
+ <field name="name">ATP10A</field>
+ <field name="long_name">ATPase, class V, type 10A</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q11-q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP13A2">
+ <field name="name">ATP13A2</field>
+ <field name="long_name">ATPase type 13A2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Parkinson disease 9 [MIM:606693]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP1A2">
+ <field name="name">ATP1A2</field>
+ <field name="long_name">ATPase, Na+/K+ transporting, alpha 2 (+) polypeptide</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21-q23</field>
+ <field name="info">
+Migraine, familial hemiplegic, 2 [MIM:602481]
+Alternating hemiplegia of childhood [MIM:104290]
+Migraine, familial basilar [MIM:602481]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP1A3">
+ <field name="name">ATP1A3</field>
+ <field name="long_name">ATPase, Na+/K+ transporting, alpha 3 polypeptide</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q12-q13.2</field>
+ <field name="info">
+Dystonia-12 [MIM:128235]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP1B1">
+ <field name="name">ATP1B1</field>
+ <field name="long_name">ATPase, Na+/K+ transporting, beta 1 polypeptide</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q22-q25</field>
+ <field name="info">
+Blood pressure regulation QTL [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP2A1">
+ <field name="name">ATP2A1</field>
+ <field name="long_name">ATPase, Ca++ transporting, cardiac muscle, fast twitch 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12</field>
+ <field name="info">
+Brody myopathy [MIM:601003]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP2A2">
+ <field name="name">ATP2A2</field>
+ <field name="long_name">ATPase, Ca++ transporting, cardiac muscle, slow twitch 2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q23-q24.1</field>
+ <field name="info">
+Darier disease [MIM:124200]
+Acrokeratosis verruciformis [MIM:101900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP2A3">
+ <field name="name">ATP2A3</field>
+ <field name="long_name">ATPase, Ca++ transporting, ubiquitous</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP2B2">
+ <field name="name">ATP2B2</field>
+ <field name="long_name">ATPase, Ca++ transporting, plasma membrane 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26-p25</field>
+ <field name="info">
+Deafness, autosomal recessive 12, modifier of [MIM:601386]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP2C1">
+ <field name="name">ATP2C1</field>
+ <field name="long_name">ATPase, Ca++ transporting, type 2C, member 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21-q24</field>
+ <field name="info">
+Hailey-Hailey disease [MIM:169600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP6AP2">
+ <field name="name">ATP6AP2</field>
+ <field name="long_name">ATPase, H+ transporting, lysosomal accessory protein 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.4</field>
+ <field name="info">
+Mental retardation, X-linked, with epilepsy [MIM:300423]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP6V0A2">
+ <field name="name">ATP6V0A2</field>
+ <field name="long_name">ATPase, H+ transporting, lysosomal V0 subunit a2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.3</field>
+ <field name="info">
+Cutis laxa, autosomal recessive, type II [MIM:219200]
+Wrinkly skin syndrome [MIM:278250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP6V0A4">
+ <field name="name">ATP6V0A4</field>
+ <field name="long_name">ATPase, H+ transporting, lysosomal V0 subunit a4</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q33-q34</field>
+ <field name="info">
+Renal tubular acidosis, distal, autosomal recessive [MIM:602722]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP7A">
+ <field name="name">ATP7A</field>
+ <field name="long_name">ATPase, Cu++ transporting, alpha polypeptide</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq12-q13</field>
+ <field name="info">
+Menkes disease [MIM:309400]
+Occipital horn syndrome [MIM:304150]
+Cutis laxa, neonatal</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP7B">
+ <field name="name">ATP7B</field>
+ <field name="long_name">ATPase, Cu++ transporting, beta polypeptide</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14.3-q21.1</field>
+ <field name="info">
+Wilson disease [MIM:277900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATP8B1">
+ <field name="name">ATP8B1</field>
+ <field name="long_name">ATPase, class I, type 8B, member 1</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21</field>
+ <field name="info">
+Cholestasis, progressive familial intrahepatic 1 [MIM:211600]
+Cholestasis, benign recurrent intrahepatic [MIM:243300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATPAF2">
+ <field name="name">ATPAF2</field>
+ <field name="long_name">ATP synthase mitochondrial F1 complex assembly factor 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+Complex V, mitochondrial respiratory chain, deficiency of [MIM:604273]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATRX">
+ <field name="name">ATRX</field>
+ <field name="long_name">alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13</field>
+ <field name="info">
+Alpha-thalassemia/mental retardation syndrome [MIM:301040]
+Alpha-thalassemia myelodysplasia syndrome, somatic [MIM:300448]
+Mental retardation-hypotonic facies syndrome, X-linked [MIM:309580]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATR">
+ <field name="name">ATR</field>
+ <field name="long_name">ataxia telangiectasia and Rad3 related</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q22-q24</field>
+ <field name="info">
+Seckel syndrome 1 [MIM:210600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATXN10">
+ <field name="name">ATXN10</field>
+ <field name="long_name">ataxin 10</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13</field>
+ <field name="info">
+Spinocerebellar ataxia-10 [MIM:603516]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATXN1">
+ <field name="name">ATXN1</field>
+ <field name="long_name">ataxin 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p23</field>
+ <field name="info">
+Spinocerebellar ataxia-1 [MIM:164400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATXN2">
+ <field name="name">ATXN2</field>
+ <field name="long_name">ataxin 2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24</field>
+ <field name="info">
+Spinocerebellar ataxia-2 [MIM:183090]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATXN3">
+ <field name="name">ATXN3</field>
+ <field name="long_name">ataxin 3</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3-q31</field>
+ <field name="info">
+Machado-Joseph disease [MIM:109150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ATXN7">
+ <field name="name">ATXN7</field>
+ <field name="long_name">ataxin 7</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.1-p12</field>
+ <field name="info">
+Spinocerebellar ataxia-7 [MIM:164500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AUH">
+ <field name="name">AUH</field>
+ <field name="long_name">AU RNA binding protein/enoyl-Coenzyme A hydratase</field>
+ <field name="chromosome">9</field>
+ <field name="location">9</field>
+ <field name="info">
+3-methylglutaconic aciduria, type I [MIM:250950]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AUNA1">
+ <field name="name">AUNA1</field>
+ <field name="long_name">auditory neuropathy, autosomal dominant 1</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14-q21</field>
+ <field name="info">
+Auditory neuropathy, autosomal dominant, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AUNX1">
+ <field name="name">AUNX1</field>
+ <field name="long_name">auditory neuropathy, X-linked recessive 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq23-q27.3</field>
+ <field name="info">
+Deafness, X-linked 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AURKA">
+ <field name="name">AURKA</field>
+ <field name="long_name">aurora kinase A</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.2-q13.3</field>
+ <field name="info">
+Colon cancer, susceptibility to [MIM:114500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AUTS11">
+ <field name="name">AUTS11</field>
+ <field name="long_name">Autism, susceptibility to, 11</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q24.2</field>
+ <field name="info">
+Autism, susceptibility to, 11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AUTS14">
+ <field name="name">AUTS14</field>
+ <field name="long_name">autism, susceptibility to, 14</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p11.2</field>
+ <field name="info">
+Autism, susceptibility to, 14</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AUTS1">
+ <field name="name">AUTS1</field>
+ <field name="long_name">autism susceptibility 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22</field>
+ <field name="info">
+Autism, susceptibility to, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AUTS3">
+ <field name="name">AUTS3</field>
+ <field name="long_name">Autism, susceptibility to, 3</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14.2-q14.1</field>
+ <field name="info">
+Autism, susceptibility to, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AUTS5">
+ <field name="name">AUTS5</field>
+ <field name="long_name">Autism, susceptibility to, 5</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q</field>
+ <field name="info">
+Autism, susceptibility to, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AUTS6">
+ <field name="name">AUTS6</field>
+ <field name="long_name">Autism, susceptibility to, 6</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11</field>
+ <field name="info">
+Autism, susceptibility to, 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AUTS7">
+ <field name="name">AUTS7</field>
+ <field name="long_name">Autism, susceptibility to, 7</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+Autism, susceptibility to, 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AVPR1B">
+ <field name="name">AVPR1B</field>
+ <field name="long_name">arginine vasopressin receptor 1B</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AVPR2">
+ <field name="name">AVPR2</field>
+ <field name="long_name">arginine vasopressin receptor 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Diabetes insipidus, nephrogenic [MIM:304800]
+Nephrogenic syndrome of inappropriate antidiuresis [MIM:300539]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AVP">
+ <field name="name">AVP</field>
+ <field name="long_name">arginine vasopressin</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p13</field>
+ <field name="info">
+Diabetes insipidus, neurohypophyseal [MIM:125700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AVSD1">
+ <field name="name">AVSD1</field>
+ <field name="long_name">atrioventricular septal defect 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31-p21</field>
+ <field name="info">
+Atrioventricular canal defect [MIM:600309]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AXIN1">
+ <field name="name">AXIN1</field>
+ <field name="long_name">axin 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+Hepatocellular carcinoma, somatic [MIM:114550]
+Caudal duplication anomaly [MIM:607864]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AXIN2">
+ <field name="name">AXIN2</field>
+ <field name="long_name">axin 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q24</field>
+ <field name="info">
+Colorectal cancer [MIM:114500]
+Oligodontia-colorectal cancer syndrome [MIM:608615]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AXL">
+ <field name="name">AXL</field>
+ <field name="long_name">AXL receptor tyrosine kinase</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1-q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="AXPC1">
+ <field name="name">AXPC1</field>
+ <field name="long_name">ataxia, posterior column 1, with retinitis pigmentosa</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31-q32</field>
+ <field name="info">
+Posterior column ataxia with retinitis pigmentosa</field>
+</record>
+<record model="gnuhealth.disease.gene" id="AZON">
+ <field name="name">AZON</field>
+ <field name="long_name">Azoospremia, nonobstructive</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Azoospremia, nonobstructive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="B2M">
+ <field name="name">B2M</field>
+ <field name="long_name">beta-2-microglobulin</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21-q22</field>
+ <field name="info">
+Hypoproteinemia, hypercatabolic [MIM:241600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="B3GALTL">
+ <field name="name">B3GALTL</field>
+ <field name="long_name">beta 1,3-galactosyltransferase-like</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12.3</field>
+ <field name="info">
+Peters-plus syndrome [MIM:261540]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="B3GNT3">
+ <field name="name">B3GNT3</field>
+ <field name="long_name">UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="B4GALT1">
+ <field name="name">B4GALT1</field>
+ <field name="long_name">UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p13</field>
+ <field name="info">
+Congenital disorder of glycosylation, type IId [MIM:607091]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="B4GALT7">
+ <field name="name">B4GALT7</field>
+ <field name="long_name">xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7 (galactosyltransferase I)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q35.2-q35.3</field>
+ <field name="info">
+Ehlers-Danlos syndrome, progeroid form [MIM:130070]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BAAT">
+ <field name="name">BAAT</field>
+ <field name="long_name">bile acid Coenzyme A: amino acid N-acyltransferase (glycine N-choloyltransferase)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22.3</field>
+ <field name="info">
+Hypercholanemia, familial [MIM:607748]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BAFME1">
+ <field name="name">BAFME1</field>
+ <field name="long_name">Myoclonic epilepsy, benign adult familial</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24</field>
+ <field name="info">
+Epilepsy, myoclonic, benign adult familial</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BAFME2">
+ <field name="name">BAFME2</field>
+ <field name="long_name">Epilepsy, myoclonic, benign adult familial, type 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p11.1-q12.2</field>
+ <field name="info">
+Epilepsy, myoclonic, benign adult familial, type 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BANK1">
+ <field name="name">BANK1</field>
+ <field name="long_name">B-cell scaffold protein with ankyrin repeats 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q22-q24</field>
+ <field name="info">
+Systemic lupus erythmatosus, association with [MIM:152700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BARD1">
+ <field name="name">BARD1</field>
+ <field name="long_name">BRCA1 associated RING domain 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q34-q35</field>
+ <field name="info">
+Breast cancer, susceptibility to [MIM:114480]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BAS">
+ <field name="name">BAS</field>
+ <field name="long_name">Beta-adrenergic stimulation, response to</field>
+ <field name="chromosome">21</field>
+ <field name="location">21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="BAT2">
+ <field name="name">BAT2</field>
+ <field name="long_name">HLA-B associated transcript 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="BAT3">
+ <field name="name">BAT3</field>
+ <field name="long_name">HLA-B associated transcript 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="BAT4">
+ <field name="name">BAT4</field>
+ <field name="long_name">HLA-B associated transcript 4</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="BAX">
+ <field name="name">BAX</field>
+ <field name="long_name">BCL2-associated X protein</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3-q13.4</field>
+ <field name="info">
+Colorectal cancer
+T-cell acute lymphoblastic leukemia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BBS10">
+ <field name="name">BBS10</field>
+ <field name="long_name">Bardet-Biedl syndrome 10</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q21.2</field>
+ <field name="info">
+Bardet-Biedel syndrome 10 [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BBS12">
+ <field name="name">BBS12</field>
+ <field name="long_name">Bardet-Biedl syndrome 12</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q27</field>
+ <field name="info">
+Bardet-Biedl syndrome 12 [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BBS1">
+ <field name="name">BBS1</field>
+ <field name="long_name">Bardet-Biedl syndrome 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Bardet-Biedl syndrome 1 [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BBS2">
+ <field name="name">BBS2</field>
+ <field name="long_name">Bardet-Biedl syndrome 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q21</field>
+ <field name="info">
+Bardet-Biedl syndrome 2 [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BBS4">
+ <field name="name">BBS4</field>
+ <field name="long_name">Bardet-Biedl syndrome 4</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22.3-q23</field>
+ <field name="info">
+Bardet-Biedl syndrome 4 [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BBS5">
+ <field name="name">BBS5</field>
+ <field name="long_name">Bardet-Biedl syndrome 5</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31</field>
+ <field name="info">
+Bardet-Biedl syndrome 5 [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BBS7">
+ <field name="name">BBS7</field>
+ <field name="long_name">Bardet-Biedl syndrome 7</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q27</field>
+ <field name="info">
+Bardet-Biedl syndrome 7 [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BBS9">
+ <field name="name">BBS9</field>
+ <field name="long_name">Bardet-Biedl syndrome 9</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14</field>
+ <field name="info">
+Bardet-Biedl syndrome 9 [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCAM">
+ <field name="name">BCAM</field>
+ <field name="long_name">basal cell adhesion molecule (Lutheran blood group)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+Blood group, Lutheran system
+Blood group, Auberger system</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCAT1">
+ <field name="name">BCAT1</field>
+ <field name="long_name">branched chain aminotransferase 1, cytosolic</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p12</field>
+ <field name="info">
+Hyperleucinemia-isoleucinemia or hypervalinemia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCAT2">
+ <field name="name">BCAT2</field>
+ <field name="long_name">branched chain aminotransferase 2, mitochondrial</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+Hypervalinemia or hyperleucine-isoleucinemia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCHE">
+ <field name="name">BCHE</field>
+ <field name="long_name">butyrylcholinesterase</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.1-q26.2</field>
+ <field name="info">
+Apnea, postanesthetic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCKDHA">
+ <field name="name">BCKDHA</field>
+ <field name="long_name">branched chain keto acid dehydrogenase E1, alpha polypeptide</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1-q13.2</field>
+ <field name="info">
+Maple syrup urine disease, type Ia [MIM:248600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCKDHB">
+ <field name="name">BCKDHB</field>
+ <field name="long_name">branched chain keto acid dehydrogenase E1, beta polypeptide</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q14</field>
+ <field name="info">
+Maple syrup urine disease, type Ib [MIM:248600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCL10">
+ <field name="name">BCL10</field>
+ <field name="long_name">B-cell CLL/lymphoma 10</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p22</field>
+ <field name="info">
+Lymphoma, MALT
+Lymphoma, follicular
+Mesothelioma
+Germ cell tumor
+Sezary syndrome
+Colon cancer</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCL11A">
+ <field name="name">BCL11A</field>
+ <field name="long_name">B-cell CLL/lymphoma 11A (zinc finger protein)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p13</field>
+ <field name="info">
+Fetal hemoglobin quantitative trait locus 5 [MIM:142335]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCL2A1">
+ <field name="name">BCL2A1</field>
+ <field name="long_name">BCL2-related protein A1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q24.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCL2">
+ <field name="name">BCL2</field>
+ <field name="long_name">B-cell CLL/lymphoma 2</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.3</field>
+ <field name="info">
+Leukemia/lymphoma, B-cell, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCL3">
+ <field name="name">BCL3</field>
+ <field name="long_name">B-cell CLL/lymphoma 3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+Leukemia/lymphoma, B-cell, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCL5">
+ <field name="name">BCL5</field>
+ <field name="long_name">B-cell CLL/lymphoma 5</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q22</field>
+ <field name="info">
+B cell prolymphocytic acute agressive leukemia with translocation t(8;17)(q24;q22),see MYC</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCL6">
+ <field name="name">BCL6</field>
+ <field name="long_name">B-cell CLL/lymphoma 6</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27</field>
+ <field name="info">
+Lymphoma, B-cell</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCL7A">
+ <field name="name">BCL7A</field>
+ <field name="long_name">B-cell CLL/lymphoma 7A</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.1</field>
+ <field name="info">
+B-cell non-Hodgkin lymphoma, high-grade</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCL8">
+ <field name="name">BCL8</field>
+ <field name="long_name">B-cell CLL/lymphoma 8</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q11-q13</field>
+ <field name="info">
+Lymphoma, diffuse large cell</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCL9">
+ <field name="name">BCL9</field>
+ <field name="long_name">B-cell CLL/lymphoma 9</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+B-cell CLL ,chronic lymphocytic leukemia with translocation t(1;14)(q21;q32),t(1;22)(q21;q11)</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCMO1">
+ <field name="name">BCMO1</field>
+ <field name="long_name">beta-carotene 15,15'-monooxygenase 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q21-q23</field>
+ <field name="info">
+Hypercarotenemia and vitamin A deficiency, autosomal dominant [MIM:115300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCOR">
+ <field name="name">BCOR</field>
+ <field name="long_name">BCL6 co-repressor</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.4</field>
+ <field name="info">
+Microphthalmia, syndromic 2 [MIM:300166]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCPR">
+ <field name="name">BCPR</field>
+ <field name="long_name">Breast cancer-related regulator of TP53</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.3</field>
+ <field name="info">
+Breast cancer</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCR">
+ <field name="name">BCR</field>
+ <field name="long_name">breakpoint cluster region</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.21</field>
+ <field name="info">
+Leukemia, chronic myeloid [MIM:608232]
+Leukemia, acute lymphocytic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BCS1L">
+ <field name="name">BCS1L</field>
+ <field name="long_name">BCS1-like (yeast)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33</field>
+ <field name="info">
+Mitochondrial complex III deficiency [MIM:124000]
+GRACILE syndrome [MIM:603358]
+Leigh syndrome [MIM:256000]
+Bjornstad syndrome [MIM:262000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BDA1B">
+ <field name="name">BDA1B</field>
+ <field name="long_name">Brachydactyly, type A1, locus B</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13.3-p13.2</field>
+ <field name="info">
+Brachydactyly, type A1 [MIM:112500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BDET">
+ <field name="name">BDET</field>
+ <field name="long_name">Bleeding disorder, east Texas type</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23</field>
+ <field name="info">
+Bleeding disorder, east Texas type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BDKRB2">
+ <field name="name">BDKRB2</field>
+ <field name="long_name">bradykinin receptor B2</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.1-q32.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="BDMF">
+ <field name="name">BDMF</field>
+ <field name="long_name">bone dysplasia with medullary fibrosarcoma</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p22-p21</field>
+ <field name="info">
+Diaphyseal medullary stenosis with malignant fibrous histiocytoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BDMR">
+ <field name="name">BDMR</field>
+ <field name="long_name">brachydactyly-mental retardation syndrome</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37</field>
+ <field name="info">
+Brachydactyly-mental retardation syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BDNF">
+ <field name="name">BDNF</field>
+ <field name="long_name">brain-derived neurotrophic factor</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13</field>
+ <field name="info">
+Memory impairment, susceptibility to
+Central hypoventilation syndrome, congenital [MIM:209880]
+Obsessive-compulsive disorder, protection against [MIM:164230]
+Bulimia nervosa, age of onset of weight loss in [MIM:607499]
+Anorexia nervosa, susceptibility to [MIM:606788]
+WAGRO syndrome [MIM:612469]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BEST1">
+ <field name="name">BEST1</field>
+ <field name="long_name">bestrophin 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Best macular dystrophy [MIM:153700]
+Maculopathy, bull's-eye
+Vitelliform macular dystrophy, adult-onset [MIM:608161]
+Bestrophinopathy [MIM:611809]
+Vitreoretinochoroidopathy [MIM:193220]
+Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma [MIM:193220]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BFHD">
+ <field name="name">BFHD</field>
+ <field name="long_name">Beukes familial hip dysplasia</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q35</field>
+ <field name="info">
+Hip dysplasia, Beukes type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BFIC2">
+ <field name="name">BFIC2</field>
+ <field name="long_name">Benign familial infantile convulsions-2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12-q12</field>
+ <field name="info">
+Convulsions, benign familial infantile, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BFIC4">
+ <field name="name">BFIC4</field>
+ <field name="long_name">Convulsions, benign familial infantile, 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.12-p35.1</field>
+ <field name="info">
+Convulsions, benign familial infantile, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BFIC">
+ <field name="name">BFIC</field>
+ <field name="long_name">benign familial infantile convulsions</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q</field>
+ <field name="info">
+Convulsions, benign familial infantile</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BFLS">
+ <field name="name">BFLS</field>
+ <field name="long_name">Borjeson-Forssman-Lehmann syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26.3</field>
+ <field name="info">
+Mental retardation, X-linked, with isolated growth hormone deficiency [MIM:300123]
+Panhypopituitarism, X-linked [MIM:312000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BFSP1">
+ <field name="name">BFSP1</field>
+ <field name="long_name">beaded filament structural protein 1, filensin</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p12.1-p11.23</field>
+ <field name="info">
+Cataract, cortical, juvenile-onset [MIM:611391]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BFSP2">
+ <field name="name">BFSP2</field>
+ <field name="long_name">beaded filament structural protein 2, phakinin</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21-q25</field>
+ <field name="info">
+Cataract, juvenile-onset [MIM:604219]
+Cataract, congenital [MIM:604219]
+Cataract, autosomal dominant, multiple types 1 [MIM:611597]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BHMT">
+ <field name="name">BHMT</field>
+ <field name="long_name">betaine-homocysteine methyltransferase</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13.1-q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="BICD1">
+ <field name="name">BICD1</field>
+ <field name="long_name">bicaudal D homolog 1 (Drosophila)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p11.2-p11.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="BIN1">
+ <field name="name">BIN1</field>
+ <field name="long_name">bridging integrator 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14</field>
+ <field name="info">
+Myopathy, centronuclear, autosomal recessive [MIM:255200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BLK">
+ <field name="name">BLK</field>
+ <field name="long_name">B lymphoid tyrosine kinase</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23-p22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="BLMH">
+ <field name="name">BLMH</field>
+ <field name="long_name">bleomycin hydrolase</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2</field>
+ <field name="info">
+Alzheimer disease, susceptibility to [MIM:104300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BLM">
+ <field name="name">BLM</field>
+ <field name="long_name">Bloom syndrome, RecQ helicase-like</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.13</field>
+ <field name="info">
+Bloom syndrome,characterized by dwarfism,sun sensitivity,immunodeficiency and a high risk for various cancers,,with increased chromosomal instability (increased large DNA deletions) and sister chromatide exchanges</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BLNK">
+ <field name="name">BLNK</field>
+ <field name="long_name">B-cell linker</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23.2</field>
+ <field name="info">
+Hypoglobulinemia and absent B cells</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BLOC1S3">
+ <field name="name">BLOC1S3</field>
+ <field name="long_name">biogenesis of lysosomal organelles complex-1, subunit 3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+Hermansky-Pudlak syndrome 8 [MIM:203300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMIQ13">
+ <field name="name">BMIQ13</field>
+ <field name="long_name">Body mass index QTL13</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14.1</field>
+ <field name="info">
+Body mass index QTL13</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMIQ14">
+ <field name="name">BMIQ14</field>
+ <field name="long_name">Body mass index QTL14</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q12.2</field>
+ <field name="info">
+Body mass index QTL14</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMIQ1">
+ <field name="name">BMIQ1</field>
+ <field name="long_name">body mass index QTL 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q32.3</field>
+ <field name="info">
+Body mass index QTL1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMIQ2">
+ <field name="name">BMIQ2</field>
+ <field name="long_name">body mass index QTL 2</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14</field>
+ <field name="info">
+Body mass index QTL2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMIQ3">
+ <field name="name">BMIQ3</field>
+ <field name="long_name">body mass index QTL 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23-q25</field>
+ <field name="info">
+Body mass index QTL3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMIQ4">
+ <field name="name">BMIQ4</field>
+ <field name="long_name">body mass index QTL 4</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Obesity, susceptibility to, BMIQ4 [MIM:607447]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMIQ5">
+ <field name="name">BMIQ5</field>
+ <field name="long_name">body mass index QTL 5</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13</field>
+ <field name="info">
+Body mass index QTL5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMIQ6">
+ <field name="name">BMIQ6</field>
+ <field name="long_name">body mass index QTL 6</field>
+ <field name="chromosome">20</field>
+ <field name="location">20pter-p11.2</field>
+ <field name="info">
+Body mass index QTL6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMND10">
+ <field name="name">BMND10</field>
+ <field name="long_name">Bone mineral density QTL 10</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24</field>
+ <field name="info">
+Bone mineral density QTL 10</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMND11">
+ <field name="name">BMND11</field>
+ <field name="long_name">Bone mineral density QTL 11</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25</field>
+ <field name="info">
+Bone mineral density QTL 11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMND13">
+ <field name="name">BMND13</field>
+ <field name="long_name">Bone mineral density QTL 13</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q23</field>
+ <field name="info">
+Bone mineral density QTL 13</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMND14">
+ <field name="name">BMND14</field>
+ <field name="long_name">Bone mineral density QTL 14</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p33-p32</field>
+ <field name="info">
+Bone mineral density QTL 14</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMND2">
+ <field name="name">BMND2</field>
+ <field name="long_name">Bone mineral density variation 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21-q23</field>
+ <field name="info">
+Bone mineral density QTL 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMND3">
+ <field name="name">BMND3</field>
+ <field name="long_name">Bone mineral density variability 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Bone mineral density QTL 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMND4">
+ <field name="name">BMND4</field>
+ <field name="long_name">Bone mineral density variation QTL 4</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq27</field>
+ <field name="info">
+Bone mineral density QTL 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMND5">
+ <field name="name">BMND5</field>
+ <field name="long_name">Bone mineral density variation QTL 5</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Bone mineral density QTL 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMND6">
+ <field name="name">BMND6</field>
+ <field name="long_name">Bone mineral density QTL 6</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.13-qter</field>
+ <field name="info">
+Bone mineral density QTL 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMND7">
+ <field name="name">BMND7</field>
+ <field name="long_name">Osteoporosis</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p12.3</field>
+ <field name="info">
+Osteoporosis [MIM:166710]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMND8">
+ <field name="name">BMND8</field>
+ <field name="long_name">Osteoporosis</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p12</field>
+ <field name="info">
+Osteoporosis [MIM:166710]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMND9">
+ <field name="name">BMND9</field>
+ <field name="long_name">Bone mineral density QTL 9</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14</field>
+ <field name="info">
+Bone mineral density QTL 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMP15">
+ <field name="name">BMP15</field>
+ <field name="long_name">bone morphogenetic protein 15</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.2</field>
+ <field name="info">
+Ovarian dysgenesis 2 [MIM:300510]
+Premature ovarian failure 4 [MIM:300510]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMP2">
+ <field name="name">BMP2</field>
+ <field name="long_name">bone morphogenetic protein 2</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p12</field>
+ <field name="info">
+HFE hemochromatosis, modifier of [MIM:235200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMP4">
+ <field name="name">BMP4</field>
+ <field name="long_name">bone morphogenetic protein 4</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q22-q23</field>
+ <field name="info">
+Microphthalmia, syndromic 6 [MIM:607932]
+Orofacial cleft 11 [MIM:600625]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMP7">
+ <field name="name">BMP7</field>
+ <field name="long_name">bone morphogenetic protein 7</field>
+ <field name="chromosome">20</field>
+ <field name="location">20</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMPR1A">
+ <field name="name">BMPR1A</field>
+ <field name="long_name">bone morphogenetic protein receptor, type IA</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.3</field>
+ <field name="info">
+Polyposis, juvenile intestinal [MIM:174900]
+Polyposis syndrome, hereditary mixed, 2 [MIM:610069]
+Juvenile polyposis syndrome, infantile form [MIM:174900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMPR1B">
+ <field name="name">BMPR1B</field>
+ <field name="long_name">bone morphogenetic protein receptor, type IB</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q23-q24</field>
+ <field name="info">
+Brachydactyly, type A2 [MIM:112600]
+Chrondrodysplasia, acromesomelic, with genital anomalies [MIM:609441]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BMPR2">
+ <field name="name">BMPR2</field>
+ <field name="long_name">bone morphogenetic protein receptor, type II (serine/threonine kinase)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33</field>
+ <field name="info">
+Pulmonary hypertension, familial primary [MIM:178600]
+Pulmonary venoocclusive disease [MIM:265450]
+Pulmonary hypertension, primary, fenfluramine-associated [MIM:178600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BOP">
+ <field name="name">BOP</field>
+ <field name="long_name">Polymicrogyria, bilateral occipital</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q16.3-q22.1</field>
+ <field name="info">
+Polymicrogyria, bilateral occipital</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BOS2">
+ <field name="name">BOS2</field>
+ <field name="long_name">Branchiootic syndrome 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31</field>
+ <field name="info">
+Branchiootic syndrome 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BPGM">
+ <field name="name">BPGM</field>
+ <field name="long_name">2,3-bisphosphoglycerate mutase</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31-q34</field>
+ <field name="info">
+Hemolytic anemia due to bisphosphoglycerate mutase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BPPV">
+ <field name="name">BPPV</field>
+ <field name="long_name">vestibulopathy, familial</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q</field>
+ <field name="info">
+Vestibulopathy, familial</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BRAF">
+ <field name="name">BRAF</field>
+ <field name="long_name">v-raf murine sarcoma viral oncogene homolog B1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q34</field>
+ <field name="info">
+Melanoma, melignant, somatic
+Colorectal cancer, somatic
+Adenocarcinoma of lung, somatic [MIM:211980]
+Nonsmall cell lung cancer, somatic
+Cardiofaciocutaneous syndrome [MIM:115150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BRCA1">
+ <field name="name">BRCA1</field>
+ <field name="long_name">breast cancer 1, early onset</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+Breast-ovarian cancer, familial, 1 [MIM:604370]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BRCA2">
+ <field name="name">BRCA2</field>
+ <field name="long_name">breast cancer 2, early onset</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12.3</field>
+ <field name="info">
+Breast-ovarian cancer, familial, 2 [MIM:612555]
+Fanconi anemia, complementation group D1 [MIM:605724]
+Prostate cancer [MIM:176807]
+Breast cancer, male, susceptibility to [MIM:114480]
+Wilms tumor [MIM:194070]
+Medulloblastoma [MIM:155255]
+Glioblastoma [MIM:137800]
+Pre-B-cell acute lymphoblastic leukemia
+Pancreatic cancer [MIM:260350]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BRCA3">
+ <field name="name">BRCA3</field>
+ <field name="long_name">breast cancer 3</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q21</field>
+ <field name="info">
+Breast cancer, type 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BRCATA">
+ <field name="name">BRCATA</field>
+ <field name="long_name">Breast cancer, 11;22 translocation associated</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Breast cancer, 11:22 translocation associated</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BRCD1">
+ <field name="name">BRCD1</field>
+ <field name="long_name">Breast cancer, ductal, suppressor-1</field>
+ <field name="chromosome">13</field>
+ <field name="location">13</field>
+ <field name="info">
+Breast cancer, ductal</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BRCD2">
+ <field name="name">BRCD2</field>
+ <field name="long_name">Breast cancer, ductal (2)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Breast cancer, ductal</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BRESEK">
+ <field name="name">BRESEK</field>
+ <field name="long_name">BRESHECK syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">X</field>
+ <field name="info">
+BRESHECK syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BRIP1">
+ <field name="name">BRIP1</field>
+ <field name="long_name">BRCA1 interacting protein C-terminal helicase 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q22</field>
+ <field name="info">
+Breast cancer, early-onset [MIM:114480]
+Fanconi anemia, complementation group J [MIM:609054]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BRKS">
+ <field name="name">BRKS</field>
+ <field name="long_name">Telopeptide lysyl hydroxylase, bone-specific</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p12</field>
+ <field name="info">
+Bruck syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BRWD3">
+ <field name="name">BRWD3</field>
+ <field name="long_name">bromodomain and WD repeat domain containing 3</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13</field>
+ <field name="info">
+Mental retardation, X-linked 93 [MIM:300659]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BSCL2">
+ <field name="name">BSCL2</field>
+ <field name="long_name">Bernardinelli-Seip congenital lipodystrophy 2 (seipin)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Lipodystrophy, congenital generalized, type 2 [MIM:269700]
+Silver spastic paraplegia syndrome [MIM:270685]
+Neuropathy, distal hereditary motor, type V [MIM:600794]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BSG">
+ <field name="name">BSG</field>
+ <field name="long_name">basigin (Ok blood group)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Blood group, OK [MIM:111380]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BSND">
+ <field name="name">BSND</field>
+ <field name="long_name">Bartter syndrome, infantile, with sensorineural deafness (Barttin)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+Bartter syndrome, type 4 [MIM:602522]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BST1">
+ <field name="name">BST1</field>
+ <field name="long_name">bone marrow stromal cell antigen 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="BSZQTL2">
+ <field name="name">BSZQTL2</field>
+ <field name="long_name">Bone size QTL</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q</field>
+ <field name="info">
+Bone size QTL</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BSZQTL3">
+ <field name="name">BSZQTL3</field>
+ <field name="long_name">Bone size quantitative trait locus 3</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24</field>
+ <field name="info">
+Bone size quantitative trait locus 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BSZQTL">
+ <field name="name">BSZQTL</field>
+ <field name="long_name">Bone size QTL</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23</field>
+ <field name="info">
+Bone size QTL</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BTBD9">
+ <field name="name">BTBD9</field>
+ <field name="long_name">BTB (POZ) domain containing 9</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21</field>
+ <field name="info">
+Restless legs syndrome, susceptibility to, 6 [MIM:611185]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BTC">
+ <field name="name">BTC</field>
+ <field name="long_name">betacellulin</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q13-q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="BTD">
+ <field name="name">BTD</field>
+ <field name="long_name">biotinidase</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25</field>
+ <field name="info">
+Biotinidase deficiency [MIM:253260]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BTK">
+ <field name="name">BTK</field>
+ <field name="long_name">Bruton agammaglobulinemia tyrosine kinase</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq21.3-q22</field>
+ <field name="info">
+Agammaglobulinemia, type 1, X-linked [MIM:300755]
+Agammaglobulinemia and isolated hormone deficiency [MIM:307200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BTNL2">
+ <field name="name">BTNL2</field>
+ <field name="long_name">butyrophilin-like 2 (MHC class II associated)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Sarcoidosis, susceptibility to, 2 [MIM:612387]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BUB1B">
+ <field name="name">BUB1B</field>
+ <field name="long_name">budding uninhibited by benzimidazoles 1 homolog beta (yeast)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15</field>
+ <field name="info">
+Colorectal cancer [MIM:114500]
+Mosaic variegated aneuploidy syndrome [MIM:257300]
+Premature chromatid separation trait [MIM:176430]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BUB1">
+ <field name="name">BUB1</field>
+ <field name="long_name">budding uninhibited by benzimidazoles 1 homolog (yeast)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14</field>
+ <field name="info">
+Colorectal cancer with chromosomal instability</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BULN">
+ <field name="name">BULN</field>
+ <field name="long_name">Bulimia nervosa, susceptibility to</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p</field>
+ <field name="info">
+Bulimia nervosa, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BWCNS">
+ <field name="name">BWCNS</field>
+ <field name="long_name">Bowen-Conradi syndrome</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.3</field>
+ <field name="info">
+Bowen-Conradi syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="BZX">
+ <field name="name">BZX</field>
+ <field name="long_name">Bazex syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24-q27</field>
+ <field name="info">
+Bazex syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C10orf2">
+ <field name="name">C10orf2</field>
+ <field name="long_name">chromosome 10 open reading frame 2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+Progressive external ophthalmoplegia with mitochondrial DNA deletions [MIM:609286]
+Sensory ataxia neuropathy, dysarthria, and ophthalmoparesis [MIM:607459]
+Mitochondrial DNA depletion syndrome, hepatocerebral form [MIM:251880]
+Spinocerebellar ataxia, infantile-onset [MIM:271245]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C14orf104">
+ <field name="name">C14orf104</field>
+ <field name="long_name">chromosome 14 open reading frame 104</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q21.3</field>
+ <field name="info">
+Ciliary dyskinesia, primary, 10 [MIM:612518]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C1GALT1C1">
+ <field name="name">C1GALT1C1</field>
+ <field name="long_name">C1GALT1-specific chaperone 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq23</field>
+ <field name="info">
+Tn syndrome [MIM:300622]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C1GALT1">
+ <field name="name">C1GALT1</field>
+ <field name="long_name">core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14-p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="C1QA">
+ <field name="name">C1QA</field>
+ <field name="long_name">complement component 1, q subcomponent, A chain</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3-p34.1</field>
+ <field name="info">
+C1q deficiency, type A</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C1QB">
+ <field name="name">C1QB</field>
+ <field name="long_name">complement component 1, q subcomponent, B chain</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3-p34.1</field>
+ <field name="info">
+C1q deficiency, type B</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C1QTNF5">
+ <field name="name">C1QTNF5</field>
+ <field name="long_name">C1q and tumor necrosis factor related protein 5</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.3</field>
+ <field name="info">
+Retinal degeneration, late-onset, autosomal dominant [MIM:605670]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C1R">
+ <field name="name">C1R</field>
+ <field name="long_name">complement component 1, r subcomponent</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+C1r/C1s deficiency, combined</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C1S">
+ <field name="name">C1S</field>
+ <field name="long_name">complement component 1, s subcomponent</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+C1r/C1s deficiency, combined
+C1s deficiency, isolated</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C20orf7">
+ <field name="name">C20orf7</field>
+ <field name="long_name">chromosome 20 open reading frame 7</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p12.1</field>
+ <field name="info">
+Mitochondrial complex 1 deficiency [MIM:252010]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C21orf33">
+ <field name="name">C21orf33</field>
+ <field name="long_name">chromosome 21 open reading frame 33</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Anophthalmia/Microphthalmia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C2orf37">
+ <field name="name">C2orf37</field>
+ <field name="long_name">chromosome 2 open reading frame 37</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q22.3-q35</field>
+ <field name="info">
+Woodhouse-Sakati syndrome [MIM:241080]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C2">
+ <field name="name">C2</field>
+ <field name="long_name">complement component 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+C2 deficiency
+Macular degeneration, age-related, reduced risk of [MIM:603075]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C3">
+ <field name="name">C3</field>
+ <field name="long_name">complement component 3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3-p13.2</field>
+ <field name="info">
+C3 deficiency
+Macular degeneration, age-related, 9 [MIM:611378]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C4A">
+ <field name="name">C4A</field>
+ <field name="long_name">complement component 4A (Rodgers blood group)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+C4 deficiency
+Blood group, Rodgers
+Systemic lupus erythematosus, susceptibility to or protection against [MIM:152700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C4BPA">
+ <field name="name">C4BPA</field>
+ <field name="long_name">complement component 4 binding protein, alpha</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="C4B">
+ <field name="name">C4B</field>
+ <field name="long_name">complement component 4B (Chido blood group)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+C4 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C5">
+ <field name="name">C5</field>
+ <field name="long_name">complement component 5</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.1</field>
+ <field name="info">
+C5 deficiency [MIM:609536]
+Liver fibrosis, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C6">
+ <field name="name">C6</field>
+ <field name="long_name">complement component 6</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13</field>
+ <field name="info">
+C6 deficiency [MIM:612446]
+Combined C6/C7 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C7orf10">
+ <field name="name">C7orf10</field>
+ <field name="long_name">chromosome 7 open reading frame 10</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="C7orf11">
+ <field name="name">C7orf11</field>
+ <field name="long_name">chromosome 7 open reading frame 11</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14</field>
+ <field name="info">
+Trichothiodystrophy, nonphotosensitive 1 [MIM:234050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C7">
+ <field name="name">C7</field>
+ <field name="long_name">complement component 7</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13</field>
+ <field name="info">
+C7 deficiency [MIM:610102]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C8A">
+ <field name="name">C8A</field>
+ <field name="long_name">complement component 8, alpha polypeptide</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+C8 deficiency, type I</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C8B">
+ <field name="name">C8B</field>
+ <field name="long_name">complement component 8, beta polypeptide</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+C8 deficiency, type II</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C8orf38">
+ <field name="name">C8orf38</field>
+ <field name="long_name">chromosome 8 open reading frame 38</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q22.1</field>
+ <field name="info">
+Leigh syndrome due to mitochondrial complex I deficiency [MIM:256000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="C9">
+ <field name="name">C9</field>
+ <field name="long_name">complement component 9</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13</field>
+ <field name="info">
+C9 deficiency
+C9 deficiency with dermatomyositis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CA1">
+ <field name="name">CA1</field>
+ <field name="long_name">carbonic anhydrase I</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CA2">
+ <field name="name">CA2</field>
+ <field name="long_name">carbonic anhydrase II</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q22</field>
+ <field name="info">
+Osteopetrosis, autosomal recessive 3, with renal tubular acidosis [MIM:259730]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CA4">
+ <field name="name">CA4</field>
+ <field name="long_name">carbonic anhydrase IV</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23</field>
+ <field name="info">
+Retinitis pigmentosa-17 [MIM:600852]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CA6">
+ <field name="name">CA6</field>
+ <field name="long_name">carbonic anhydrase VI</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.33-p36.22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CAA">
+ <field name="name">CAA</field>
+ <field name="long_name">Aural atresia, congenital</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q22.3-q23</field>
+ <field name="info">
+Aural atresia, congenital</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CABC1">
+ <field name="name">CABC1</field>
+ <field name="long_name">chaperone, ABC1 activity of bc1 complex homolog (S. pombe)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42.2</field>
+ <field name="info">
+Coenzyme Q10 deficiency [MIM:607426]
+Spinocerebellar ataxia, autosomal recessive 9 [MIM:612016]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CABP4">
+ <field name="name">CABP4</field>
+ <field name="long_name">calcium binding protein 4</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.1</field>
+ <field name="info">
+Night blindness, congenital stationary, type 2B [MIM:610427]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CACD">
+ <field name="name">CACD</field>
+ <field name="long_name">central areolar choroidal dystrophy</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p</field>
+ <field name="info">
+Choroidal dystrophy, central areolar</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CACNA1A">
+ <field name="name">CACNA1A</field>
+ <field name="long_name">calcium channel, voltage-dependent, P/Q type, alpha 1A subunit</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13</field>
+ <field name="info">
+Hemiplegic migraine, familial [MIM:141500]
+Episodic ataxia, type 2 [MIM:108500]
+Spinocerebellar ataxia-6 [MIM:183086]
+Cerebellar ataxia, pure</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CACNA1C">
+ <field name="name">CACNA1C</field>
+ <field name="long_name">calcium channel, voltage-dependent, L type, alpha 1C subunit</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.3</field>
+ <field name="info">
+Timothy syndrome [MIM:601005]
+Brugada syndrome 3 [MIM:611875]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CACNA1E">
+ <field name="name">CACNA1E</field>
+ <field name="long_name">calcium channel, voltage-dependent, R type, alpha 1E subunit</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q25-q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CACNA1F">
+ <field name="name">CACNA1F</field>
+ <field name="long_name">calcium channel, voltage-dependent, L type, alpha 1F subunit</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23</field>
+ <field name="info">
+Night blindness, congenital stationary, X-linked, type 2A [MIM:300071]
+Cone-rod dystrophy, X-linked, 3 [MIM:300476]
+Aland Island eye disease [MIM:300600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CACNA1G">
+ <field name="name">CACNA1G</field>
+ <field name="long_name">calcium channel, voltage-dependent, T type, alpha 1G subunit</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CACNA1H">
+ <field name="name">CACNA1H</field>
+ <field name="long_name">calcium channel, voltage-dependent, T type, alpha 1H subunit</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+Epilepsy, idiopathic generalized, susceptibility to, 6 [MIM:611942]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CACNA1S">
+ <field name="name">CACNA1S</field>
+ <field name="long_name">calcium channel, voltage-dependent, L type, alpha 1S subunit</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+Hypokalemic periodic paralysis [MIM:170400]
+Malignant hyperthermia susceptibility 5 [MIM:601887]
+Thyrotoxic periodic paralysis, susceptibility to [MIM:188580]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CACNA2D4">
+ <field name="name">CACNA2D4</field>
+ <field name="long_name">calcium channel, voltage-dependent, alpha 2/delta subunit 4</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.3</field>
+ <field name="info">
+Retinal cone dystrophy 4 [MIM:610478]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CACNB2">
+ <field name="name">CACNB2</field>
+ <field name="long_name">calcium channel, voltage-dependent, beta 2 subunit</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p12</field>
+ <field name="info">
+Brugada syndrome 4 [MIM:611876]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CACNB4">
+ <field name="name">CACNB4</field>
+ <field name="long_name">calcium channel, voltage-dependent, beta 4 subunit</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q22-q23</field>
+ <field name="info">
+Epilepsy, juvenile myoclonic [MIM:606904]
+Epilepsy, generalized idiopathic [MIM:600669]
+Episodic ataxia, type 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CACNG2">
+ <field name="name">CACNG2</field>
+ <field name="long_name">calcium channel, voltage-dependent, gamma subunit 2</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CALCA">
+ <field name="name">CALCA</field>
+ <field name="long_name">calcitonin-related polypeptide alpha</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.2-p15.1</field>
+ <field name="info">
+Osteoporosis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CALCR">
+ <field name="name">CALCR</field>
+ <field name="long_name">calcitonin receptor</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.3</field>
+ <field name="info">
+Osteoporosis, postmenopausal, susceptibility [MIM:166710]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CALHM1">
+ <field name="name">CALHM1</field>
+ <field name="long_name">calcium homeostasis modulator 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24.33</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CALM1">
+ <field name="name">CALM1</field>
+ <field name="long_name">calmodulin 1 (phosphorylase kinase, delta)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24-q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CALR3">
+ <field name="name">CALR3</field>
+ <field name="long_name">calreticulin 3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CALR">
+ <field name="name">CALR</field>
+ <field name="long_name">calreticulin</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CANDN1">
+ <field name="name">CANDN1</field>
+ <field name="long_name">candidiasis, nail 1 (with ICAM1 deficiency)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13-q12</field>
+ <field name="info">
+Candidiasis, familial chronic nail, with ICAM1 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CAPN10">
+ <field name="name">CAPN10</field>
+ <field name="long_name">calpain 10</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.3</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent 1 [MIM:601283]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CAPN3">
+ <field name="name">CAPN3</field>
+ <field name="long_name">calpain 3, (p94)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15.1-q21.1</field>
+ <field name="info">
+Muscular dystrophy, limb-girdle, type 2A [MIM:253600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CAQ14">
+ <field name="name">CAQ14</field>
+ <field name="long_name">Circulating adiponectin QTL on chromosome 14</field>
+ <field name="chromosome">14</field>
+ <field name="location">14p11.2-q13</field>
+ <field name="info">
+Adiponectin, serum level of, QTL3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CAQ5">
+ <field name="name">CAQ5</field>
+ <field name="long_name">Circulating adiponectin QTL on chromosome 5</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.2-p14</field>
+ <field name="info">
+Adiponectin, serum level of, QTL2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CARD8">
+ <field name="name">CARD8</field>
+ <field name="long_name">caspase recruitment domain family, member 8</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CASK">
+ <field name="name">CASK</field>
+ <field name="long_name">calcium/calmodulin-dependent serine protein kinase (MAGUK family)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.4</field>
+ <field name="info">
+Mental retardation and microcephaly with pontine and cerebellar hypoplasia [MIM:300749]
+FG syndrome 4 [MIM:300422]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CASP10">
+ <field name="name">CASP10</field>
+ <field name="long_name">caspase 10, apoptosis-related cysteine peptidase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33-q34</field>
+ <field name="info">
+Autoimmune lymphoproliferative syndrome, type II [MIM:603909]
+Non-Hodgkin lymphoma, somatic [MIM:605027]
+Gastric cancer, somatic [MIM:137215]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CASP12">
+ <field name="name">CASP12</field>
+ <field name="long_name">caspase 12 (gene/pseudogene)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22.3</field>
+ <field name="info">
+Sepsis, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CASP3">
+ <field name="name">CASP3</field>
+ <field name="long_name">caspase 3, apoptosis-related cysteine peptidase</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q35</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CASP8">
+ <field name="name">CASP8</field>
+ <field name="long_name">caspase 8, apoptosis-related cysteine peptidase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33</field>
+ <field name="info">
+Autoimmune lymphoproliferative syndrome, type IIB [MIM:607271]
+Hepatocellular carcinoma, somatic [MIM:114550]
+Breast cancer, protection against [MIM:114480]
+Lung cancer, protection against [MIM:211980]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CASQ2">
+ <field name="name">CASQ2</field>
+ <field name="long_name">calsequestrin 2 (cardiac muscle)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13.3-p11</field>
+ <field name="info">
+Ventricular tachycardia, catecholaminergic polymorphic, 2 [MIM:611938]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CASR">
+ <field name="name">CASR</field>
+ <field name="long_name">calcium-sensing receptor</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q13.3-q21</field>
+ <field name="info">
+Hypocalciuric hypercalcemia, type I [MIM:145980]
+Hyperparathyroidism, neonatal [MIM:239200]
+Hypocalcemia, autosomal dominant [MIM:146200]
+Hypocalcemia, autosomal dominant, with Bartter syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CAST">
+ <field name="name">CAST</field>
+ <field name="long_name">calpastatin</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q15-q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CATC2">
+ <field name="name">CATC2</field>
+ <field name="long_name">Cataract, autosomal recessive congenital 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p22-p21</field>
+ <field name="info">
+Cataract, autosomal recessive congenital 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CAT">
+ <field name="name">CAT</field>
+ <field name="long_name">catalase</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13</field>
+ <field name="info">
+Acatalasemia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CAV1">
+ <field name="name">CAV1</field>
+ <field name="long_name">caveolin 1, caveolae protein, 22kDa</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31.1</field>
+ <field name="info">
+Lipodystrophy, congenital generalized, type 3 [MIM:612526]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CAV3">
+ <field name="name">CAV3</field>
+ <field name="long_name">caveolin 3</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25</field>
+ <field name="info">
+Muscular dystrophy, limb-girdle, type IC [MIM:607801]
+Rippling muscle disease [MIM:606072]
+Creatine phosphokinase, elevated serum [MIM:123320]
+Myopathy, distal, with decreased caveolin 3
+Cardiomyopathy, familial hypertrophic [MIM:192600]
+Long QT syndrome-9 [MIM:611818]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CBFB">
+ <field name="name">CBFB</field>
+ <field name="long_name">core-binding factor, beta subunit</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22</field>
+ <field name="info">
+Myeloid leukemia, acute, M4Eo subtype</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CBLB">
+ <field name="name">CBLB</field>
+ <field name="long_name">Cas-Br-M (murine) ecotropic retroviral transforming sequence b</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CBL">
+ <field name="name">CBL</field>
+ <field name="long_name">Cas-Br-M (murine) ecotropic retroviral transforming sequence</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CBR1">
+ <field name="name">CBR1</field>
+ <field name="long_name">carbonyl reductase 1</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CBR3">
+ <field name="name">CBR3</field>
+ <field name="long_name">carbonyl reductase 3</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CBS">
+ <field name="name">CBS</field>
+ <field name="long_name">cystathionine-beta-synthase</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Homocystinuria, B6-responsive and nonresponsive types
+Thrombosis, hyperhomocysteinemic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CC2D1A">
+ <field name="name">CC2D1A</field>
+ <field name="long_name">coiled-coil and C2 domain containing 1A</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.12</field>
+ <field name="info">
+Mental retardation, autosomal recessive 3 [MIM:608443]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CC2D2A">
+ <field name="name">CC2D2A</field>
+ <field name="long_name">coiled-coil and C2 domain containing 2A</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15.3</field>
+ <field name="info">
+Joubert syndrome 9 [MIM:612285]
+Meckel syndrome, type 6 [MIM:612284]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCA1">
+ <field name="name">CCA1</field>
+ <field name="long_name">cataract, congenital, cerulean type, 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q24</field>
+ <field name="info">
+Cataract, cerulean, type 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCAL1">
+ <field name="name">CCAL1</field>
+ <field name="long_name">chondrocalcinosis 1 (calcium pyrophosphate-deposition disease, early onset osteoarthritis)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q</field>
+ <field name="info">
+Chondrocalcinosis with early-onset osteoarthritis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCDC50">
+ <field name="name">CCDC50</field>
+ <field name="long_name">coiled-coil domain containing 50</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q28</field>
+ <field name="info">
+Deafness, autosomal dominant 44 [MIM:607453]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCDC6">
+ <field name="name">CCDC6</field>
+ <field name="long_name">coiled-coil domain containing 6</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21</field>
+ <field name="info">
+Thyroid papillary carcinoma [MIM:188550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCKAR">
+ <field name="name">CCKAR</field>
+ <field name="long_name">cholecystokinin A receptor</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15.2-p15.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCKBR">
+ <field name="name">CCKBR</field>
+ <field name="long_name">cholecystokinin B receptor</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5-p15.4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCK">
+ <field name="name">CCK</field>
+ <field name="long_name">cholecystokinin</field>
+ <field name="chromosome">3</field>
+ <field name="location">3pter-p21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCL11">
+ <field name="name">CCL11</field>
+ <field name="long_name">chemokine (C-C motif) ligand 11</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.1-q21.2</field>
+ <field name="info">
+HIV1, resistance to [MIM:609423]
+Asthma, susceptibility to [MIM:600807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCL13">
+ <field name="name">CCL13</field>
+ <field name="long_name">chemokine (C-C motif) ligand 13</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCL17">
+ <field name="name">CCL17</field>
+ <field name="long_name">chemokine (C-C motif) ligand 17</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCL26">
+ <field name="name">CCL26</field>
+ <field name="long_name">chemokine (C-C motif) ligand 26</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.2</field>
+ <field name="info">
+Esophagitis, eosinophilic, susceptibility to [MIM:610247]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCL2">
+ <field name="name">CCL2</field>
+ <field name="long_name">chemokine (C-C motif) ligand 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2-q12</field>
+ <field name="info">
+HIV-1, resistance to [MIM:609423]
+Spina bifida, susceptiblity to [MIM:182940]
+Coronary artery disease, modifier of
+Mycobacterium tuberculosis, susceptibility to [MIM:607948]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCL3L1">
+ <field name="name">CCL3L1</field>
+ <field name="long_name">chemokine (C-C motif) ligand 3-like 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2</field>
+ <field name="info">
+HIV/AIDS, susceptibility to [MIM:609423]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCL3">
+ <field name="name">CCL3</field>
+ <field name="long_name">chemokine (C-C motif) ligand 3</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12</field>
+ <field name="info">
+HIV infection, resistance to [MIM:609423]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCL5">
+ <field name="name">CCL5</field>
+ <field name="long_name">chemokine (C-C motif) ligand 5</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2-q12</field>
+ <field name="info">
+HIV-1 disease, delayed progression of
+HIV-1 disease, rapid progression of</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCM2">
+ <field name="name">CCM2</field>
+ <field name="long_name">cerebral cavernous malformation 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p13</field>
+ <field name="info">
+Cerebral cavernous malformations-2 [MIM:603284]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCND1">
+ <field name="name">CCND1</field>
+ <field name="long_name">cyclin D1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Colorectal cancer, susceptibility to [MIM:114500]
+von Hippel-Lindau disease, modification of [MIM:193300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCNP">
+ <field name="name">CCNP</field>
+ <field name="long_name">Cataract, congenital, nuclear progressive</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p12</field>
+ <field name="info">
+Cataract, nuclear progressive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCR1">
+ <field name="name">CCR1</field>
+ <field name="long_name">chemokine (C-C motif) receptor 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCR2">
+ <field name="name">CCR2</field>
+ <field name="long_name">chemokine (C-C motif) receptor 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21</field>
+ <field name="info">
+HIV infection, susceptibility/resistance to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCR5">
+ <field name="name">CCR5</field>
+ <field name="long_name">chemokine (C-C motif) receptor 5</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21</field>
+ <field name="info">
+HIV infection, susceptibility/resistance to
+West nile virus, susceptibility to [MIM:610379]
+Hepatitis C virus, resistance to [MIM:609532]
+Diabetes mellitus, insulin-dependent, 22 [MIM:612522]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCR7">
+ <field name="name">CCR7</field>
+ <field name="long_name">chemokine (C-C motif) receptor 7</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12-q21.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCT5">
+ <field name="name">CCT5</field>
+ <field name="long_name">chaperonin containing TCP1, subunit 5 (epsilon)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.2</field>
+ <field name="info">
+Neuropathy, hereditary sensory, with spastic paraplegia [MIM:256840]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCT">
+ <field name="name">CCT</field>
+ <field name="long_name">cataract, congenital, total</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp</field>
+ <field name="info">
+Cataract, congenital total</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CCV">
+ <field name="name">CCV</field>
+ <field name="long_name">cataract, congenital, Volkmann type</field>
+ <field name="chromosome">1</field>
+ <field name="location">1pter-p36.13</field>
+ <field name="info">
+Cataract, congenital, Volkmann type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD109">
+ <field name="name">CD109</field>
+ <field name="long_name">CD109 molecule</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD14">
+ <field name="name">CD14</field>
+ <field name="long_name">CD14 molecule</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD151">
+ <field name="name">CD151</field>
+ <field name="long_name">CD151 molecule (Raph blood group)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Nephropathy with pretibial epidermolysis bullosa and deafness [MIM:609057]
+Blood group, Raph [MIM:179620]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD177">
+ <field name="name">CD177</field>
+ <field name="long_name">CD177 molecule</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD19">
+ <field name="name">CD19</field>
+ <field name="long_name">CD19 molecule</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p11.2</field>
+ <field name="info">
+Antibody deficiency due to defect in CD19</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD1A">
+ <field name="name">CD1A</field>
+ <field name="long_name">CD1a molecule</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21-q23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD1E">
+ <field name="name">CD1E</field>
+ <field name="long_name">CD1e molecule</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21-q23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD207">
+ <field name="name">CD207</field>
+ <field name="long_name">CD207 molecule, langerin</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD209">
+ <field name="name">CD209</field>
+ <field name="long_name">CD209 molecule</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Dengue fever, protection against
+HIV type 1, susceptibility to [MIM:609423]
+Mycobacterium tuberculosis, susceptibility to [MIM:607948]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD244">
+ <field name="name">CD244</field>
+ <field name="long_name">CD244 molecule, natural killer cell receptor 2B4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q22</field>
+ <field name="info">
+Rheumatoid arthritis, susceptibility to [MIM:180300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD247">
+ <field name="name">CD247</field>
+ <field name="long_name">CD247 molecule</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q22-q23</field>
+ <field name="info">
+Immunodeficiency due to defect in CD3-zeta [MIM:610163]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD24">
+ <field name="name">CD24</field>
+ <field name="long_name">CD24 molecule</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+Multiple sclerosis, susceptibility to [MIM:126200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD2AP">
+ <field name="name">CD2AP</field>
+ <field name="long_name">CD2-associated protein</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12</field>
+ <field name="info">
+Glomerulosclerosis, focal segmental, 3 [MIM:607832]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD36">
+ <field name="name">CD36</field>
+ <field name="long_name">CD36 molecule (thrombospondin receptor)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.2</field>
+ <field name="info">
+Macrothrombocytopenia
+Platelet glycoprotein IV deficiency [MIM:608404]
+Malaria, cerebral, susceptibility to [MIM:611162]
+Malaria, cerebral, reduced risk of [MIM:611162]
+Coronary heart disease, susceptibility to, 7 [MIM:610938]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD38">
+ <field name="name">CD38</field>
+ <field name="long_name">CD38 molecule</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD3D">
+ <field name="name">CD3D</field>
+ <field name="long_name">CD3d molecule, delta (CD3-TCR complex)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Severe combined immunodeficiency, T cell-negative, B-cell/natural killer-cell positive [MIM:608971]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD3E">
+ <field name="name">CD3E</field>
+ <field name="long_name">CD3e molecule, epsilon (CD3-TCR complex)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Immunodeficiency due to defect in CD3-epsilon
+Severe combined immunodeficiency, T cell-negative, B-cell/natural killer-cell positive [MIM:608971]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD3G">
+ <field name="name">CD3G</field>
+ <field name="long_name">CD3g molecule, gamma (CD3-TCR complex)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Immunodeficiency due to defect in CD3-gamma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD40LG">
+ <field name="name">CD40LG</field>
+ <field name="long_name">CD40 ligand</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26</field>
+ <field name="info">
+Immunodeficiency, X-linked, with hyper-IgM [MIM:308230]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD40">
+ <field name="name">CD40</field>
+ <field name="long_name">CD40 molecule, TNF receptor superfamily member 5</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q12-q13.2</field>
+ <field name="info">
+Immunodeficiency with hyper-IgM, type 3 [MIM:606843]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD44">
+ <field name="name">CD44</field>
+ <field name="long_name">CD44 molecule (Indian blood group)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11pter-p13</field>
+ <field name="info">
+Blood group, Indian system</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD46">
+ <field name="name">CD46</field>
+ <field name="long_name">CD46 molecule, complement regulatory protein</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+Hemolytic-uremic syndrome [MIM:235400]
+Measles, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD4">
+ <field name="name">CD4</field>
+ <field name="long_name">CD4 molecule</field>
+ <field name="chromosome">12</field>
+ <field name="location">12pter-p12</field>
+ <field name="info">
+CD4+ lymphocyte deficiency
+Lupus erythematosus, susceptibility to (2) 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD55">
+ <field name="name">CD55</field>
+ <field name="long_name">CD55 molecule, decay accelerating factor for complement (Cromer blood group)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+Blood group Cromer</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD59">
+ <field name="name">CD59</field>
+ <field name="long_name">CD59 molecule, complement regulatory protein</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13</field>
+ <field name="info">
+CD59 deficiency [MIM:612300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD72">
+ <field name="name">CD72</field>
+ <field name="long_name">CD72 molecule</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD79A">
+ <field name="name">CD79A</field>
+ <field name="long_name">CD79a molecule, immunoglobulin-associated alpha</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD79B">
+ <field name="name">CD79B</field>
+ <field name="long_name">CD79b molecule, immunoglobulin-associated beta</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23</field>
+ <field name="info">
+Immunodeficiency, hypogammaglobulinemia, and reduced B cells [MIM:612692]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD82">
+ <field name="name">CD82</field>
+ <field name="long_name">CD82 molecule</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p11.2</field>
+ <field name="info">
+Prostate cancer, susceptibility to [MIM:176807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD86">
+ <field name="name">CD86</field>
+ <field name="long_name">CD86 molecule</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD8A">
+ <field name="name">CD8A</field>
+ <field name="long_name">CD8a molecule</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p12</field>
+ <field name="info">
+CD8 deficiency, familial [MIM:608957]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CD96">
+ <field name="name">CD96</field>
+ <field name="long_name">CD96 molecule</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q13.13</field>
+ <field name="info">
+C syndrome [MIM:211750]
+C-like syndrome [MIM:605039]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDAGS">
+ <field name="name">CDAGS</field>
+ <field name="long_name">Craniosynostosis, anal anomalies, and porokeratosis syndrome</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12-q13</field>
+ <field name="info">
+CDAGS syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDAN1">
+ <field name="name">CDAN1</field>
+ <field name="long_name">congenital dyserythropoietic anemia, type I</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15</field>
+ <field name="info">
+Anemia, congenital dyserythropoietic, type I [MIM:224120]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDAN2">
+ <field name="name">CDAN2</field>
+ <field name="long_name">congenital dyserythropoietic anemia, type II</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11.2</field>
+ <field name="info">
+Congenital dyserythropoietic anemia II</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDAN3">
+ <field name="name">CDAN3</field>
+ <field name="long_name">congenital dyserythropoietic anemia, type III</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21</field>
+ <field name="info">
+Dyserythropoietic anemia, congenital, type III</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDA">
+ <field name="name">CDA</field>
+ <field name="long_name">cytidine deaminase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2-p35</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDB2">
+ <field name="name">CDB2</field>
+ <field name="long_name">corneal dystrophy of Bowman layer type II (Thiel-Behnke)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+Corneal dystrophy, Thiel-Behnke type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDC2L2">
+ <field name="name">CDC2L2</field>
+ <field name="long_name">cell division cycle 2-like 2 (PITSLRE proteins)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDC6">
+ <field name="name">CDC6</field>
+ <field name="long_name">cell division cycle 6 homolog (S. cerevisiae)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDH12">
+ <field name="name">CDH12</field>
+ <field name="long_name">cadherin 12, type 2 (N-cadherin 2)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p14-p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDH15">
+ <field name="name">CDH15</field>
+ <field name="long_name">cadherin 15, type 1, M-cadherin (myotubule)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.3</field>
+ <field name="info">
+Mental retardation, autosomal dominant 3 [MIM:612580]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDH1">
+ <field name="name">CDH1</field>
+ <field name="long_name">cadherin 1, type 1, E-cadherin (epithelial)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22.1</field>
+ <field name="info">
+Endometrial carcinoma
+Ovarian carcinoma
+Breast cancer, lobular
+Gastric cancer, familial diffuse [MIM:137215]
+Listeria monocytogenes, susceptibility to
+Cleft lip with or without cleft palate, with gastric cancer, familial diffuse</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDH23">
+ <field name="name">CDH23</field>
+ <field name="long_name">cadherin-like 23</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21-q22</field>
+ <field name="info">
+Usher syndrome, type 1D [MIM:601067]
+Deafness, autosomal recessive 12 [MIM:601386]
+Usher syndrome, type 1D/F digenic [MIM:601067]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDH3">
+ <field name="name">CDH3</field>
+ <field name="long_name">cadherin 3, type 1, P-cadherin (placental)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22.1</field>
+ <field name="info">
+Hypotrichosis, congenital, with juvenile macular dystrophy [MIM:601553]
+Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MIM:225280]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDK4">
+ <field name="name">CDK4</field>
+ <field name="long_name">cyclin-dependent kinase 4</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q14</field>
+ <field name="info">
+Melanoma [MIM:609048]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDK5RAP2">
+ <field name="name">CDK5RAP2</field>
+ <field name="long_name">CDK5 regulatory subunit associated protein 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q33.3</field>
+ <field name="info">
+Microcephaly, primary autosomal recessive, 3 [MIM:604804]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDK7">
+ <field name="name">CDK7</field>
+ <field name="long_name">cyclin-dependent kinase 7</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p15-cen</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDKAL1">
+ <field name="name">CDKAL1</field>
+ <field name="long_name">CDK5 regulatory subunit associated protein 1-like 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p22.3</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent, susceptibility to [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDKL3">
+ <field name="name">CDKL3</field>
+ <field name="long_name">cyclin-dependent kinase-like 3</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDKL5">
+ <field name="name">CDKL5</field>
+ <field name="long_name">cyclin-dependent kinase-like 5</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22</field>
+ <field name="info">
+Epileptic encephalopathy, early infantile, 2 [MIM:300672]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDKN1A">
+ <field name="name">CDKN1A</field>
+ <field name="long_name">cyclin-dependent kinase inhibitor 1A (p21, Cip1)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDKN1B">
+ <field name="name">CDKN1B</field>
+ <field name="long_name">cyclin-dependent kinase inhibitor 1B (p27, Kip1)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+Multiple endocrine neoplasia, type IV [MIM:610755]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDKN1C">
+ <field name="name">CDKN1C</field>
+ <field name="long_name">cyclin-dependent kinase inhibitor 1C (p57, Kip2)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Beckwith-Wiedemann syndrome [MIM:130650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDKN2A">
+ <field name="name">CDKN2A</field>
+ <field name="long_name">cyclin-dependent kinase inhibitor 2A (melanoma, p16, inhibits CDK4)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21</field>
+ <field name="info">
+Melanoma, cutaneous malignant, 2 [MIM:155601]
+Li Fraumeni syndrome [MIM:151623]
+Melanoma and neural system tumor syndrome [MIM:155755]
+Pancreatic cancer/melanoma syndrome [MIM:606719]
+Orolaryngeal cancer, multiple </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDKN2B">
+ <field name="name">CDKN2B</field>
+ <field name="long_name">cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDPD1">
+ <field name="name">CDPD1</field>
+ <field name="long_name">corneal dystrophy and perceptive deafness 1</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p13</field>
+ <field name="info">
+Corneal dystrophy and perceptive deafness 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDSN">
+ <field name="name">CDSN</field>
+ <field name="long_name">corneodesmosin</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Hypotrichosis simplex of scalp [MIM:146520]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CDY1">
+ <field name="name">CDY1</field>
+ <field name="long_name">chromodomain protein, Y-linked, 1</field>
+ <field name="chromosome">Y</field>
+ <field name="location">Y</field>
+ <field name="info">
+Y Chromosome Infertility</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CEBPA">
+ <field name="name">CEBPA</field>
+ <field name="long_name">CCAAT/enhancer binding protein (C/EBP), alpha</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+Leukemia, acute myeloid [MIM:601626]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CEBPE">
+ <field name="name">CEBPE</field>
+ <field name="long_name">CCAAT/enhancer binding protein (C/EBP), epsilon</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2</field>
+ <field name="info">
+Specific granule deficiency [MIM:245480]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CECR">
+ <field name="name">CECR</field>
+ <field name="long_name">cat eye syndrome chromosome region</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11</field>
+ <field name="info">
+Cat eye syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CELIAC10">
+ <field name="name">CELIAC10</field>
+ <field name="long_name">Celiac disease, susceptibility to, 10</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q25-q26</field>
+ <field name="info">
+Celiac disease, susceptibility to, 10</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CELIAC11">
+ <field name="name">CELIAC11</field>
+ <field name="long_name">Celiac disease, susceptibility to, 11</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q28</field>
+ <field name="info">
+Celiac disease, susceptibility to, 11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CELIAC12">
+ <field name="name">CELIAC12</field>
+ <field name="long_name">Celiac disease, susceptibility to, 12</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25.3</field>
+ <field name="info">
+Celiac disease, susceptibility to, 12</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CELIAC13">
+ <field name="name">CELIAC13</field>
+ <field name="long_name">Celiac disease, susceptibility to, 13</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24</field>
+ <field name="info">
+Celiac disease, susceptibility to, 13</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CELIAC2">
+ <field name="name">CELIAC2</field>
+ <field name="long_name">celiac disease 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31-q33</field>
+ <field name="info">
+Celiac disease, susceptibility to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CELIAC5">
+ <field name="name">CELIAC5</field>
+ <field name="long_name">Celiac disease, susceptibility to, 5</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q11-q13</field>
+ <field name="info">
+Celiac disease, susceptibility to, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CELIAC6">
+ <field name="name">CELIAC6</field>
+ <field name="long_name">Celiac disease, susceptibility to, 6</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q27</field>
+ <field name="info">
+Celiac disease, susceptibility to, 6
+Autoimmune disease, susceptibility to, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CELIAC7">
+ <field name="name">CELIAC7</field>
+ <field name="long_name">Celiac disease, susceptibility to, 7</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31</field>
+ <field name="info">
+Celiac disease, susceptibility to, 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CELIAC8">
+ <field name="name">CELIAC8</field>
+ <field name="long_name">Celiac disease, susceptibility to, 8</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q11-q12</field>
+ <field name="info">
+Celiac disease, susceptibility to, 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CELIAC9">
+ <field name="name">CELIAC9</field>
+ <field name="long_name">Celiac disease, susceptibility to, 9</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21</field>
+ <field name="info">
+Celiac disease, susceptibility to, 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CEL">
+ <field name="name">CEL</field>
+ <field name="long_name">carboxyl ester lipase (bile salt-stimulated lipase)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.3</field>
+ <field name="info">
+Maturity-onset diabetes of the young, type VIII [MIM:609812]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CEP290">
+ <field name="name">CEP290</field>
+ <field name="long_name">centrosomal protein 290kDa</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q21.3</field>
+ <field name="info">
+Joubert syndrome 5 [MIM:610188]
+Senior-Loken syndrome 6 [MIM:610189]
+Leber congenital amaurosis 10 [MIM:611755]
+Meckel syndrome type 4 [MIM:611134]
+Bardet-Biedl syndrome 14 [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CER1">
+ <field name="name">CER1</field>
+ <field name="long_name">cerberus 1, cysteine knot superfamily, homolog (Xenopus laevis)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CERKL">
+ <field name="name">CERKL</field>
+ <field name="long_name">ceramide kinase-like</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31.2-q32.3</field>
+ <field name="info">
+Retinitis pigmentosa-26 [MIM:608380]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CES1">
+ <field name="name">CES1</field>
+ <field name="long_name">carboxylesterase 1 (monocyte/macrophage serine esterase 1)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q13-q22.1</field>
+ <field name="info">
+Carboxylesterase 1 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CETP">
+ <field name="name">CETP</field>
+ <field name="long_name">cholesteryl ester transfer protein, plasma</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q21</field>
+ <field name="info">
+CETP deficiency [MIM:607322]
+Hyperalphalipoproteinemia [MIM:143470]
+High density lipoprotein cholesterol level QTL 10</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CFB">
+ <field name="name">CFB</field>
+ <field name="long_name">complement factor B</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Macular degeneration, age-related, reduced risk of [MIM:603075]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CFC1">
+ <field name="name">CFC1</field>
+ <field name="long_name">cripto, FRL-1, cryptic family 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q21.1</field>
+ <field name="info">
+Heterotaxy, visceral, 2, autosomal [MIM:605376]
+Double-outlet right ventricle [MIM:217095]
+Transposition of the great arteries, dextro-looped 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CFD">
+ <field name="name">CFD</field>
+ <field name="long_name">complement factor D (adipsin)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Complement factor D deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CFH">
+ <field name="name">CFH</field>
+ <field name="long_name">complement factor H</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+Hemolytic-uremic syndrome [MIM:235400]
+Factor H and factor H-like 1 [MIM:609814]
+Membranoproliferative glomerulonephritis with CFH deficiency [MIM:609814]
+Macular degeneration, age-related, 4 [MIM:610698]
+Complement factor H deficiency [MIM:609814]
+Myocardial infarction, susceptibility to
+Basal laminar drusen [MIM:126700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CFL2">
+ <field name="name">CFL2</field>
+ <field name="long_name">cofilin 2 (muscle)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q12</field>
+ <field name="info">
+Nemaline myopathy 7 [MIM:610687]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CFM1">
+ <field name="name">CFM1</field>
+ <field name="long_name">cystic fibrosis modifier 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2-q13.4</field>
+ <field name="info">
+Meconium ileus in cystic fibrosis, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CFSS">
+ <field name="name">CFSS</field>
+ <field name="long_name">craniofacioskeletal syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26-q27</field>
+ <field name="info">
+Craniofacioskeletal syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CFTD2">
+ <field name="name">CFTD2</field>
+ <field name="long_name">Myopathy, congenital, with fiber-type disproportion 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.1-q22.1</field>
+ <field name="info">
+Myopathy, congenital, with fiber-type disproportion 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CFTR">
+ <field name="name">CFTR</field>
+ <field name="long_name">cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31.2</field>
+ <field name="info">
+Cystic fibrosis [MIM:219700]
+Congenital bilateral absence of vas deferens [MIM:277180]
+Sweat chloride elevation without CF
+Pancreatitis, idiopathic
+Hypertrypsinemia, neonatal</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CGB">
+ <field name="name">CGB</field>
+ <field name="long_name">chorionic gonadotropin, beta polypeptide</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CGF1">
+ <field name="name">CGF1</field>
+ <field name="long_name">cognitive function 1, social</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq</field>
+ <field name="info">
+Social cognition</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHAT">
+ <field name="name">CHAT</field>
+ <field name="long_name">choline acetyltransferase</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q11.2</field>
+ <field name="info">
+Myasthenic syndrome, congenital, associated with episodic apnea [MIM:254210]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHD2">
+ <field name="name">CHD2</field>
+ <field name="long_name">chromodomain helicase DNA binding protein 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHD7">
+ <field name="name">CHD7</field>
+ <field name="long_name">chromodomain helicase DNA binding protein 7</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q12.1</field>
+ <field name="info">
+CHARGE syndrome [MIM:214800]
+Scoliosis, idiopathic 3 [MIM:608765]
+Kallmann syndrome 5 [MIM:612370]
+Hypogonadotropic hypogonadism [MIM:146110]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHDM">
+ <field name="name">CHDM</field>
+ <field name="long_name">Chordoma</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q33</field>
+ <field name="info">
+Chordoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHDS1">
+ <field name="name">CHDS1</field>
+ <field name="long_name">Coronary heart disease, susceptibility to, 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16pter-p13</field>
+ <field name="info">
+Coronary heart disease, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHDS2">
+ <field name="name">CHDS2</field>
+ <field name="long_name">Coronary heart disease, susceptibility to, 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q21.1-q22</field>
+ <field name="info">
+Coronary heart disease, susceptibility to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHDS3">
+ <field name="name">CHDS3</field>
+ <field name="long_name">Coronary heart disease, susceptibility to, 3</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq23-q26</field>
+ <field name="info">
+Coronary heart disease, susceptibility to, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHDS4">
+ <field name="name">CHDS4</field>
+ <field name="long_name">Coronary heart disease, susceptibility to, 4</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32</field>
+ <field name="info">
+Coronary heart disease, susceptibility to, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHDS8">
+ <field name="name">CHDS8</field>
+ <field name="long_name">Coronary heart disease, susceptibility to, 8</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21</field>
+ <field name="info">
+Coronary heart disease, susceptibility to, 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHDS9">
+ <field name="name">CHDS9</field>
+ <field name="long_name">Coronary heart disease, suscpetibility to, 9</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p22</field>
+ <field name="info">
+Coronary heart disease, suscpetibility to, 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHED1">
+ <field name="name">CHED1</field>
+ <field name="long_name">corneal endothelial dystrophy 1 (autosomal dominant)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p11.2-q11.2</field>
+ <field name="info">
+Congenital hereditary endothelial dystrophy of cornea, autosomal dominant</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHEK2">
+ <field name="name">CHEK2</field>
+ <field name="long_name">CHK2 checkpoint homolog (S. pombe)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.1</field>
+ <field name="info">
+Li-Fraumeni syndrome [MIM:609265]
+Osteosarcoma, somatic [MIM:259500]
+Breast cancer, susceptibility to [MIM:114480]
+Prostate cancer, familial [MIM:176807]
+Breast and colorectal cancer, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHFR">
+ <field name="name">CHFR</field>
+ <field name="long_name">checkpoint with forkhead and ring finger domains</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.33</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHGA">
+ <field name="name">CHGA</field>
+ <field name="long_name">chromogranin A (parathyroid secretory protein 1)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHGB">
+ <field name="name">CHGB</field>
+ <field name="long_name">chromogranin B (secretogranin 1)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20pter-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHI3L1">
+ <field name="name">CHI3L1</field>
+ <field name="long_name">chitinase 3-like 1 (cartilage glycoprotein-39)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32.1</field>
+ <field name="info">
+Schizophrenia, susceptiblity to [MIM:181500]
+Asthma-related traits, susceptibility to, 7 [MIM:611960]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHIC2">
+ <field name="name">CHIC2</field>
+ <field name="long_name">cysteine-rich hydrophobic domain 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q11-q12</field>
+ <field name="info">
+Leukemia, acute myeloid [MIM:601626]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHL1">
+ <field name="name">CHL1</field>
+ <field name="long_name">cell adhesion molecule with homology to L1CAM (close homolog of L1)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHMP2B">
+ <field name="name">CHMP2B</field>
+ <field name="long_name">chromatin modifying protein 2B</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p11.2</field>
+ <field name="info">
+Dementia, familial, nonspecific [MIM:600795]
+Amyotrophic lateral sclerosis, CHMP2B-related</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHMP4B">
+ <field name="name">CHMP4B</field>
+ <field name="long_name">chromatin modifying protein 4B</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11.21</field>
+ <field name="info">
+Cataract, posterior polar, 3 [MIM:605387]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHM">
+ <field name="name">CHM</field>
+ <field name="long_name">choroideremia (Rab escort protein 1)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq21.2</field>
+ <field name="info">
+Choroideremia [MIM:303100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHN1">
+ <field name="name">CHN1</field>
+ <field name="long_name">chimerin (chimaerin) 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31-q32.1</field>
+ <field name="info">
+Duane retraction syndrome 2 [MIM:604356]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHNG3">
+ <field name="name">CHNG3</field>
+ <field name="long_name">Hypothyroidism, congenital, nongoitrous, 3</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q25.3-q26.1</field>
+ <field name="info">
+Hypothyroidism, congenital, nongoitrous, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRM2">
+ <field name="name">CHRM2</field>
+ <field name="long_name">cholinergic receptor, muscarinic 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q35-q36</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRM3">
+ <field name="name">CHRM3</field>
+ <field name="long_name">cholinergic receptor, muscarinic 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q41-q44</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRNA1">
+ <field name="name">CHRNA1</field>
+ <field name="long_name">cholinergic receptor, nicotinic, alpha 1 (muscle)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q24-q32</field>
+ <field name="info">
+Myasthenic syndrome, slow-channel congenital [MIM:601462]
+Myasthenic syndrome, fast-channel congenital [MIM:608930]
+Multiple pterygium syndrome, lethal type [MIM:253290]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRNA2">
+ <field name="name">CHRNA2</field>
+ <field name="long_name">cholinergic receptor, nicotinic, alpha 2 (neuronal)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21</field>
+ <field name="info">
+Epilepsy, nocturnal frontal lobe, type 4 [MIM:610353]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRNA3">
+ <field name="name">CHRNA3</field>
+ <field name="long_name">cholinergic receptor, nicotinic, alpha 3</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q25.1</field>
+ <field name="info">
+Lung cancer susceptibility 2 [MIM:612052]
+Peripheral arterial occlusive disease [MIM:612052]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRNA4">
+ <field name="name">CHRNA4</field>
+ <field name="long_name">cholinergic receptor, nicotinic, alpha 4</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.2-q13.3</field>
+ <field name="info">
+Epilepsy, nocturnal frontal lobe, 1 [MIM:600513]
+Nicotine addiction, susceptibility to [MIM:188890]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRNA5">
+ <field name="name">CHRNA5</field>
+ <field name="long_name">cholinergic receptor, nicotinic, alpha 5</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q25.1</field>
+ <field name="info">
+Lung cancer susceptibility 2 [MIM:612052]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRNA7">
+ <field name="name">CHRNA7</field>
+ <field name="long_name">cholinergic receptor, nicotinic, alpha 7</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q14</field>
+ <field name="info">
+Schizophrenia, neurophysiologic defect in</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRNB1">
+ <field name="name">CHRNB1</field>
+ <field name="long_name">cholinergic receptor, nicotinic, beta 1 (muscle)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p12-p11</field>
+ <field name="info">
+Myasthenic syndrome, slow-channel congenital [MIM:601462]
+Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency [MIM:608931]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRNB2">
+ <field name="name">CHRNB2</field>
+ <field name="long_name">cholinergic receptor, nicotinic, beta 2 (neuronal)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Epilepsy, nocturnal frontal lobe, 3 [MIM:605375]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRNB4">
+ <field name="name">CHRNB4</field>
+ <field name="long_name">cholinergic receptor, nicotinic, beta 4</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRND">
+ <field name="name">CHRND</field>
+ <field name="long_name">cholinergic receptor, nicotinic, delta</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33-q34</field>
+ <field name="info">
+Myasthenic syndrome, slow-channel congenital [MIM:601462]
+Myasthenic syndrome, fast-channel congenital [MIM:608930]
+Multiple pterygium syndrome, lethal type [MIM:253290]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRNE">
+ <field name="name">CHRNE</field>
+ <field name="long_name">cholinergic receptor, nicotinic, epsilon</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13-p12</field>
+ <field name="info">
+Myasthenic syndrome, slow-channel congenital [MIM:601462]
+Myasthenic syndrome, fast-channel congenital [MIM:608930]
+Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency [MIM:608931]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHRNG">
+ <field name="name">CHRNG</field>
+ <field name="long_name">cholinergic receptor, nicotinic, gamma</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33-q34</field>
+ <field name="info">
+Myasthenia gravis, neonatal transient
+Escobar syndrome [MIM:265000]
+Multiple pterygium syndrome, lethal type [MIM:253290]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHST3">
+ <field name="name">CHST3</field>
+ <field name="long_name">carbohydrate (chondroitin 6) sulfotransferase 3</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.1</field>
+ <field name="info">
+Spondyloepiphyseal dysplasia, Omani type [MIM:608637]
+Humerospinal dysostosis [MIM:143095]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CHST6">
+ <field name="name">CHST6</field>
+ <field name="long_name">carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22</field>
+ <field name="info">
+Macular corneal dystrophy [MIM:217800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CILD2">
+ <field name="name">CILD2</field>
+ <field name="long_name">ciliary dyskinesia, primary 2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3-qter</field>
+ <field name="info">
+Ciliary dyskinesia, primary, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CILD4">
+ <field name="name">CILD4</field>
+ <field name="long_name">Ciliary dyskinesia, primary, 4</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q13.1-q15.1</field>
+ <field name="info">
+Ciliary dyskinesia, primary, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CILD5">
+ <field name="name">CILD5</field>
+ <field name="long_name">Ciliary dyskinesia, primary, 5</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12.2-p12.1</field>
+ <field name="info">
+Ciliary dyskinesia, primary, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CILD8">
+ <field name="name">CILD8</field>
+ <field name="long_name">Ciliary dyskinesia, primary, 8</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q24-q25</field>
+ <field name="info">
+Ciliary dyskinesia, primary, 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CILP">
+ <field name="name">CILP</field>
+ <field name="long_name">cartilage intermediate layer protein, nucleotide pyrophosphohydrolase</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22</field>
+ <field name="info">
+Lumbar disc disease, susceptibility to [MIM:603932]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CIMT">
+ <field name="name">CIMT</field>
+ <field name="long_name">Carotid intimal medial thickness</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24</field>
+ <field name="info">
+Carotid intimal medial thickness</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CINN">
+ <field name="name">CINN</field>
+ <field name="long_name">Cinnamon odor, pleasantness of</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q32.3</field>
+ <field name="info">
+Cinnamon odor, pleasantness of</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CIRH1A">
+ <field name="name">CIRH1A</field>
+ <field name="long_name">cirrhosis, autosomal recessive 1A (cirhin)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22</field>
+ <field name="info">
+Cirrhosis, North American Indian childhood type [MIM:604901]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CISD2">
+ <field name="name">CISD2</field>
+ <field name="long_name">CDGSH iron sulfur domain 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q22-q24</field>
+ <field name="info">
+Wolfram syndrome 2 [MIM:604928]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CITED2">
+ <field name="name">CITED2</field>
+ <field name="long_name">Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CKBE">
+ <field name="name">CKBE</field>
+ <field name="long_name">creatine kinase, ectopic expression</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32</field>
+ <field name="info">
+Creatine kinase, brain type, ectopic expression of</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CKM">
+ <field name="name">CKM</field>
+ <field name="long_name">creatine kinase, muscle</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLAM">
+ <field name="name">CLAM</field>
+ <field name="long_name">cerebellar atrophy with progressive microcephaly</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11-q21</field>
+ <field name="info">
+Cerebellar atrophy with progressive microcephaly</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLCA2">
+ <field name="name">CLCA2</field>
+ <field name="long_name">chloride channel accessory 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31-p22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLCF1">
+ <field name="name">CLCF1</field>
+ <field name="long_name">cardiotrophin-like cytokine factor 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.3</field>
+ <field name="info">
+Cold-induced sweating syndrome 1 [MIM:610313]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLCN1">
+ <field name="name">CLCN1</field>
+ <field name="long_name">chloride channel 1, skeletal muscle</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q35</field>
+ <field name="info">
+Myotonia congenita, recessive [MIM:255700]
+Myotonia congenita, dominant [MIM:160800]
+Myotonia levior, recessive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLCN2">
+ <field name="name">CLCN2</field>
+ <field name="long_name">chloride channel 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26-qter</field>
+ <field name="info">
+Epilepsy with grand mal seizures on awakening [MIM:607628]
+Epilepsy, juvenile myoclonic [MIM:606904]
+Epilepsy, childhood absence [MIM:607682]
+Epilepsy, juvenile absence [MIM:607631]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLCN5">
+ <field name="name">CLCN5</field>
+ <field name="long_name">chloride channel 5</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.22</field>
+ <field name="info">
+Dent disease [MIM:300009]
+Nephrolithiasis, type I [MIM:310468]
+Hypophosphatemic rickets [MIM:300554]
+Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis [MIM:308990]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLCN6">
+ <field name="name">CLCN6</field>
+ <field name="long_name">chloride channel 6</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Neuronal Ceroid-Lipofuscinoses</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLCN7">
+ <field name="name">CLCN7</field>
+ <field name="long_name">chloride channel 7</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13</field>
+ <field name="info">
+Osteopetrosis, autosomal recessive 4 [MIM:611490]
+Osteopetrosis, autosomal dominant 2 [MIM:166600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLCNKA">
+ <field name="name">CLCNKA</field>
+ <field name="long_name">chloride channel Ka</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Bartter syndrome, type 4, digenic [MIM:602522]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLCNKB">
+ <field name="name">CLCNKB</field>
+ <field name="long_name">chloride channel Kb</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Bartter syndrome, type 3 [MIM:607364]
+Bartter syndrome, type 4, digenic [MIM:602522]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLDN14">
+ <field name="name">CLDN14</field>
+ <field name="long_name">claudin 14</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Deafness, autosomal recessive 29</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLDN16">
+ <field name="name">CLDN16</field>
+ <field name="long_name">claudin 16</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27</field>
+ <field name="info">
+Hypomagnesemia, primary [MIM:248250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLDN19">
+ <field name="name">CLDN19</field>
+ <field name="long_name">claudin 19</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34.2</field>
+ <field name="info">
+Hypomagnesemia, renal, with ocular involvement [MIM:248190]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLDN1">
+ <field name="name">CLDN1</field>
+ <field name="long_name">claudin 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q28-q29</field>
+ <field name="info">
+Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis [MIM:607626]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLEC4M">
+ <field name="name">CLEC4M</field>
+ <field name="long_name">C-type lectin domain family 4, member M</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+SARS infection, protection against</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLF">
+ <field name="name">CLF</field>
+ <field name="long_name">cholesterol-lowering factor</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q</field>
+ <field name="info">
+Cholesterol level QTL 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLK2">
+ <field name="name">CLK2</field>
+ <field name="long_name">CDC-like kinase 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLLS1">
+ <field name="name">CLLS1</field>
+ <field name="long_name">Leukemia, chronic lymphocytic, susceptibility to, 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.3</field>
+ <field name="info">
+Leukemia, chronic lymphocytic, susceptibility to, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLLS3">
+ <field name="name">CLLS3</field>
+ <field name="long_name">Leukemia, chronic lymphocytic, susceptibility to, 3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.1</field>
+ <field name="info">
+Leukemia, chronic lymphocytic, susceptibility to, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLLS4">
+ <field name="name">CLLS4</field>
+ <field name="long_name">Leukemia, chronic lymphocytic susceptibility to, 4</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p25</field>
+ <field name="info">
+Leukemia, chronic lymphocytic susceptibility to, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLLS5">
+ <field name="name">CLLS5</field>
+ <field name="long_name">Leukemia, chronic lymphocytic susceptiblity to, 5</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q24.1</field>
+ <field name="info">
+Leukemia, chronic lymphocytic susceptiblity to, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLN3">
+ <field name="name">CLN3</field>
+ <field name="long_name">ceroid-lipofuscinosis, neuronal 3</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12.1</field>
+ <field name="info">
+Ceroid-lipofuscinosis, neuronal-3, juvenile [MIM:204200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLN5">
+ <field name="name">CLN5</field>
+ <field name="long_name">ceroid-lipofuscinosis, neuronal 5</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q21.1-q32</field>
+ <field name="info">
+Ceroid-lipofuscinosis, neuronal-5, variant late infantile [MIM:256731]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLN6">
+ <field name="name">CLN6</field>
+ <field name="long_name">ceroid-lipofuscinosis, neuronal 6, late infantile, variant</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21-q23</field>
+ <field name="info">
+Ceroid-lipofuscinosis, neuronal-6, variant late infantile [MIM:601780]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLN8">
+ <field name="name">CLN8</field>
+ <field name="long_name">ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23</field>
+ <field name="info">
+Ceroid lipofuscinosis, neuronal 8 [MIM:600143]
+Ceroid lipofuscinosis, neuronal, 8, Northern epilepsy variant [MIM:610003]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLOCK">
+ <field name="name">CLOCK</field>
+ <field name="long_name">clock homolog (mouse)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLPS">
+ <field name="name">CLPS</field>
+ <field name="long_name">colipase, pancreatic</field>
+ <field name="chromosome">6</field>
+ <field name="location">6pter-p21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLPTM1">
+ <field name="name">CLPTM1</field>
+ <field name="long_name">cleft lip and palate associated transmembrane protein 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.33</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLQTL2">
+ <field name="name">CLQTL2</field>
+ <field name="long_name">Cholesterol level QTL 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p24-p22</field>
+ <field name="info">
+Cholesterol level QTL 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLTCL1">
+ <field name="name">CLTCL1</field>
+ <field name="long_name">clathrin, heavy chain-like 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CLU">
+ <field name="name">CLU</field>
+ <field name="long_name">clusterin</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMA1">
+ <field name="name">CMA1</field>
+ <field name="long_name">chymase 1, mast cell</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMAL">
+ <field name="name">CMAL</field>
+ <field name="long_name">Capillary malformations, hereditary</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13-q22</field>
+ <field name="info">
+Capillary malformations, hereditary</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMCT">
+ <field name="name">CMCT</field>
+ <field name="long_name">Candidiasis, familial chronic mucocutaneous, autosomal dominant, with thyroid disease</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p</field>
+ <field name="info">
+Candidiasis, familial chronic mucocutaneous, autosomal dominant, with thyroid disease</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMD1B">
+ <field name="name">CMD1B</field>
+ <field name="long_name">cardiomyopathy, dilated 1B (autosomal dominant)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q13</field>
+ <field name="info">
+Cardiomyopathy, familial dilated 1B</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMD1C">
+ <field name="name">CMD1C</field>
+ <field name="long_name">cardiomyopathy, dilated 1C (autosomal dominant)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21-q23</field>
+ <field name="info">
+Cardiomyopathy, dilated, 1C</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMD1D">
+ <field name="name">CMD1D</field>
+ <field name="long_name">cardiomyopathy, dilated 1D (autosomal dominant)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+Cardiomyopathy, familial hypertrophic, 2 [MIM:115195]
+Cardiomyopathy, dilated, 1D [MIM:601494]
+Cardiomyopathy, familial restrictive, 3 [MIM:612422]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMD1F">
+ <field name="name">CMD1F</field>
+ <field name="long_name">cardiomyopathy, dilated 1F (autosomal dominant)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23</field>
+ <field name="info">
+Cardiomyopathy, dilated, 1F</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMD1H">
+ <field name="name">CMD1H</field>
+ <field name="long_name">cardiomyopathy, dilated 1H (autosomal dominant)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14-q22</field>
+ <field name="info">
+Cardiomyopathy, dilated, 1H</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMD1K">
+ <field name="name">CMD1K</field>
+ <field name="long_name">cardiomyopathy, dilated 1K (autosomal dominant)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q12-q16</field>
+ <field name="info">
+Cardiomyopathy, dilated, 1K</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMD1Q">
+ <field name="name">CMD1Q</field>
+ <field name="long_name">cardiomyopathy, dilated 1Q (autosomal dominant)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22.3-q31.1</field>
+ <field name="info">
+Cardiomyopathy, dilated, 1Q</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMD2A">
+ <field name="name">CMD2A</field>
+ <field name="long_name">cardiomyopathy, dilated 2A (autosomal recessive)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+Cardiomyopathy, familial hypertrophic, 7
+Cardiomyopathy, familial restrictive [MIM:115210]
+Cardiomyopathy, dilated, 2A [MIM:611880]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMDJ">
+ <field name="name">CMDJ</field>
+ <field name="long_name">craniometaphyseal dysplasia, Jackson type (dominant)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.2-p14.1</field>
+ <field name="info">
+Craniometaphyseal dysplasia [MIM:123000]
+Chondrocalcinosis 2 [MIM:118600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMDR">
+ <field name="name">CMDR</field>
+ <field name="long_name">Craniometaphyseal dysplasia, autosomal recessive</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21-q22</field>
+ <field name="info">
+Craniometaphyseal dysplasia, autosomal recessive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMH3">
+ <field name="name">CMH3</field>
+ <field name="long_name">cardiomyopathy, hypertrophic 3</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22.1</field>
+ <field name="info">
+Cardiomyopathy, familial hypertrophic, 3 [MIM:115196]
+Cardiomyopathy, dilated, 1Y [MIM:611878]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMM4">
+ <field name="name">CMM4</field>
+ <field name="long_name">Melanoma, cutaneous malignant, 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p22</field>
+ <field name="info">
+Melanoma, cutaneous malignant, 4 [MIM:155600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMM7">
+ <field name="name">CMM7</field>
+ <field name="long_name">Melanoma, cutaneous malignant, susceptibility to, 7</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11.2</field>
+ <field name="info">
+Melanoma, cutaneous malignant, susceptibility to, 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMM">
+ <field name="name">CMM</field>
+ <field name="long_name">cutaneous malignant melanoma/dysplastic nevus</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Malignant melanoma, cutaneous</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMPK1">
+ <field name="name">CMPK1</field>
+ <field name="long_name">cytidine monophosphate (UMP-CMP) kinase 1, cytosolic</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMT1A">
+ <field name="name">CMT1A</field>
+ <field name="long_name">Charcot-Marie-Tooth neuropathy 1A (greatly reduced nerve conduction velocity, hereditary motor sensory neuropathy Ia)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 1A [MIM:118220]
+Dejerine-Sottas disease [MIM:145900]
+Neuropathy, recurrent, with pressure palsies [MIM:162500]
+Charcot-Marie-Tooth disease, type 1E [MIM:118300]
+Roussy-Levy syndrome [MIM:180800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMT2B2">
+ <field name="name">CMT2B2</field>
+ <field name="long_name">Charcot-Marie-Tooth disease, axonal, type 2B2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 2B2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMT2B">
+ <field name="name">CMT2B</field>
+ <field name="long_name">Charcot-Marie-Tooth neuropathy 2B</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 2B [MIM:600882]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMT2C">
+ <field name="name">CMT2C</field>
+ <field name="long_name">Charcot-Marie-Tooth disease, axonal, type 2C</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q23-q24</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 2C</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMT2G">
+ <field name="name">CMT2G</field>
+ <field name="long_name">Charcot-Marie-Tooth disease, axonal, type 2G</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q12-q13.3</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, axonal, type 2G</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMTDI2">
+ <field name="name">CMTDI2</field>
+ <field name="long_name">Charcot-Marie-Tooth disease, dominant intermediate 2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24.1-q25.1</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, dominant intermediate 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMTX2">
+ <field name="name">CMTX2</field>
+ <field name="long_name">Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.2</field>
+ <field name="info">
+Charcot-Marie-Tooth neuropathy, X-linked recessive, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CMTX3">
+ <field name="name">CMTX3</field>
+ <field name="long_name">Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26</field>
+ <field name="info">
+Charcot-Marie-Tooth neuropathy, X-linked recessive, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CND">
+ <field name="name">CND</field>
+ <field name="long_name">Corneal dermoids</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24-qter</field>
+ <field name="info">
+Dermoids of cornea</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CNGA1">
+ <field name="name">CNGA1</field>
+ <field name="long_name">cyclic nucleotide gated channel alpha 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p12-cen</field>
+ <field name="info">
+Retinitis pigmentosa, autosomal recessive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CNGA3">
+ <field name="name">CNGA3</field>
+ <field name="long_name">cyclic nucleotide gated channel alpha 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q11</field>
+ <field name="info">
+Achromatopsia-2 [MIM:216900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CNGB1">
+ <field name="name">CNGB1</field>
+ <field name="long_name">cyclic nucleotide gated channel beta 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q13</field>
+ <field name="info">
+Retinitis pigmentosa, autosomal recessive [MIM:268000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CNGB3">
+ <field name="name">CNGB3</field>
+ <field name="long_name">cyclic nucleotide gated channel beta 3</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21-q22</field>
+ <field name="info">
+Achromatopsia-3 [MIM:262300]
+Macular degeneration, juvenile [MIM:248200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CNNM4">
+ <field name="name">CNNM4</field>
+ <field name="long_name">cyclin M4</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p12-p11.2</field>
+ <field name="info">
+Jalili syndrome [MIM:217080]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CNR1">
+ <field name="name">CNR1</field>
+ <field name="long_name">cannabinoid receptor 1 (brain)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q14-q15</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CNSN">
+ <field name="name">CNSN</field>
+ <field name="long_name">Carnosinemia (carnosinase)</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.3</field>
+ <field name="info">
+Carnosinemia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CNTF">
+ <field name="name">CNTF</field>
+ <field name="long_name">ciliary neurotrophic factor</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q12.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CNTN1">
+ <field name="name">CNTN1</field>
+ <field name="long_name">contactin 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q11-q12</field>
+ <field name="info">
+Myopathy, congenital, Compton-North [MIM:612540]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CNTN4">
+ <field name="name">CNTN4</field>
+ <field name="long_name">contactin 4</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26-p25</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CNTNAP2">
+ <field name="name">CNTNAP2</field>
+ <field name="long_name">contactin associated protein-like 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q35-q36</field>
+ <field name="info">
+Cortical dysplasia-focal epilepsy syndrome [MIM:610042]
+Autism, susceptibility to, 15 [MIM:612100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COCH">
+ <field name="name">COCH</field>
+ <field name="long_name">coagulation factor C homolog, cochlin (Limulus polyphemus)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q12-q13</field>
+ <field name="info">
+Deafness, autosomal dominant 9 [MIM:601369]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COD2">
+ <field name="name">COD2</field>
+ <field name="long_name">cone dystrophy 2 (X-linked)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq27</field>
+ <field name="info">
+Cone dystrophy, progressive X-linked, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CODA">
+ <field name="name">CODA</field>
+ <field name="long_name">Cavitary optic disc anomalies</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q</field>
+ <field name="info">
+Cavitary optic disc anomalies</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COG1">
+ <field name="name">COG1</field>
+ <field name="long_name">component of oligomeric golgi complex 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25.1</field>
+ <field name="info">
+Congenital disorder of glycosylation, type IIg [MIM:611209]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COG7">
+ <field name="name">COG7</field>
+ <field name="long_name">component of oligomeric golgi complex 7</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p</field>
+ <field name="info">
+Congenital disorder of glycosylation, type IIe [MIM:608779]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COG8">
+ <field name="name">COG8</field>
+ <field name="long_name">component of oligomeric golgi complex 8</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22.1</field>
+ <field name="info">
+Congenital disorder of glycosylation, type IIh [MIM:611182]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL10A1">
+ <field name="name">COL10A1</field>
+ <field name="long_name">collagen, type X, alpha 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21-q22.3</field>
+ <field name="info">
+Metaphyseal chondrodysplasia, Schmid type
+Spondylometaphyseal dysplasia, Japanese type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL11A1">
+ <field name="name">COL11A1</field>
+ <field name="long_name">collagen, type XI, alpha 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p21</field>
+ <field name="info">
+Stickler syndrome, type II [MIM:604841]
+Marshall syndrome [MIM:154780]
+Lumbar disc herniation, susceptibility to [MIM:603932]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL11A2">
+ <field name="name">COL11A2</field>
+ <field name="long_name">collagen, type XI, alpha 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Stickler syndrome, type III [MIM:184840]
+Otospondylomegaepiphyseal dysplasia [MIM:215150]
+Weissenbacher-Zweymuller syndrome [MIM:277610]
+Deafness, autosomal dominant 13 [MIM:601868]
+Deafness, autosomal recessive 53 [MIM:609706]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL17A1">
+ <field name="name">COL17A1</field>
+ <field name="long_name">collagen, type XVII, alpha 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24.3</field>
+ <field name="info">
+Epidermolysis bullosa, junctional, non-Herlitz type [MIM:226650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL18A1">
+ <field name="name">COL18A1</field>
+ <field name="long_name">collagen, type XVIII, alpha 1</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Knobloch syndrome, type 1 [MIM:267750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL1A1">
+ <field name="name">COL1A1</field>
+ <field name="long_name">collagen, type I, alpha 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.31-q22</field>
+ <field name="info">
+Osteogenesis imperfecta, type I [MIM:166200]
+OI type II [MIM:166210]
+OI type III [MIM:259420]
+OI type IV [MIM:166220]
+Ehlers-Danlos syndrome, type I [MIM:130000]
+Ehlers-Danlos syndrome, type VII [MIM:130060]
+Osteoporosis [MIM:166710]
+Dissection of cervical arteries
+Caffey disease [MIM:114000]
+OI/EDS combined syndrome (3) 11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL1A2">
+ <field name="name">COL1A2</field>
+ <field name="long_name">collagen, type I, alpha 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22.1</field>
+ <field name="info">
+Osteogenesis imperfecta, 3 clinical forms, 166200, 166210 [MIM:259420]
+Ehlers-Danlos syndrome, type VIIB [MIM:130060]
+Osteoporosis, postmenopausal [MIM:166710]
+Marfan syndrome, atypical
+Ehlers-Danlos syndrome, cardiac valvular form [MIM:225320]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL29A1">
+ <field name="name">COL29A1</field>
+ <field name="long_name">collagen, type XXIX, alpha 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL2A1">
+ <field name="name">COL2A1</field>
+ <field name="long_name">collagen, type II, alpha 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13.11-q13.2</field>
+ <field name="info">
+Stickler syndrome, type I [MIM:108300]
+Kniest dysplasia [MIM:156550]
+Achondrogenesis-hypochondrogenesis, type II [MIM:200610]
+SED congenita [MIM:183900]
+SMED Strudwick type [MIM:184250]
+Epiphyseal dysplasia, multiple, with myopia and deafness [MIM:132450]
+Spondyloperipheral dysplasia [MIM:271700]
+SED, Namaqualand type
+Osteoarthritis with mild chondrodysplasia [MIM:604864]
+Vitreoretinopathy with phalangeal epiphyseal dysplasia
+Platyspondylic skeletal dysplasia, Torrance type [MIM:151210]
+Otospondylomegaepiphyseal dysplasia [MIM:215150]
+Avascular necrosis of the femoral head [MIM:608805]
+Legg-Calve-Perthes disease [MIM:150600]
+Stickler sydrome, type I, nonsyndromic ocular [MIM:609508]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL3A1">
+ <field name="name">COL3A1</field>
+ <field name="long_name">collagen, type III, alpha 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31</field>
+ <field name="info">
+Ehlers-Danlos syndrome, type IV [MIM:130050]
+Ehlers-Danlos syndrome, type III [MIM:130020]
+Aneurysm, familial arterial</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL4A1">
+ <field name="name">COL4A1</field>
+ <field name="long_name">collagen, type IV, alpha 1</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q34</field>
+ <field name="info">
+Porencephaly [MIM:175780]
+Brain small vessel disease with hemorrhage [MIM:607595]
+Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps [MIM:611773]
+Brain small vessel disease with Axenfeld-Rieger anomaly [MIM:607595]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL4A3">
+ <field name="name">COL4A3</field>
+ <field name="long_name">collagen, type IV, alpha 3 (Goodpasture antigen)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q36-q37</field>
+ <field name="info">
+Alport syndrome, autosomal recessive [MIM:203780]
+Hematuria, benign familial [MIM:141200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL4A4">
+ <field name="name">COL4A4</field>
+ <field name="long_name">collagen, type IV, alpha 4</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q36-q37</field>
+ <field name="info">
+Alport syndrome, autosomal recessive [MIM:203780]
+Hematuria, familial benign</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL4A5">
+ <field name="name">COL4A5</field>
+ <field name="long_name">collagen, type IV, alpha 5</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22.3</field>
+ <field name="info">
+Alport syndrome [MIM:301050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL4A6">
+ <field name="name">COL4A6</field>
+ <field name="long_name">collagen, type IV, alpha 6</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22.3</field>
+ <field name="info">
+Leiomyomatosis, diffuse, with Alport syndrome [MIM:308940]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL5A1">
+ <field name="name">COL5A1</field>
+ <field name="long_name">collagen, type V, alpha 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.2-q34.3</field>
+ <field name="info">
+Ehlers-Danlos syndrome, type II [MIM:130010]
+Ehlers-Danlos syndrome, type I [MIM:130000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL5A2">
+ <field name="name">COL5A2</field>
+ <field name="long_name">collagen, type V, alpha 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31</field>
+ <field name="info">
+Ehlers-Danlos syndrome, type I [MIM:130000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL6A1">
+ <field name="name">COL6A1</field>
+ <field name="long_name">collagen, type VI, alpha 1</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Bethlem myopathy [MIM:158810]
+Ullrich congenital muscular dystrophy [MIM:254090]
+Ossification of the posterior longitudinal spinal ligaments [MIM:602475]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL6A2">
+ <field name="name">COL6A2</field>
+ <field name="long_name">collagen, type VI, alpha 2</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Bethlem myopathy [MIM:158810]
+Ullrich congenital muscular dystrophy [MIM:254090]
+Myosclerosis, congenital [MIM:255600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL6A3">
+ <field name="name">COL6A3</field>
+ <field name="long_name">collagen, type VI, alpha 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37</field>
+ <field name="info">
+Bethlem myopathy [MIM:158810]
+Ullrich congenital muscular dystrophy [MIM:254090]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL7A1">
+ <field name="name">COL7A1</field>
+ <field name="long_name">collagen, type VII, alpha 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.3</field>
+ <field name="info">
+Epidermolysis bullosa dystrophica, AD [MIM:131750]
+Epidermolysis bullosa dystrophica, AR [MIM:226600]
+Epidermolysis bullosa, pretibial [MIM:131850]
+EBD, Bart type [MIM:132000]
+EBD, localisata variant
+Transient bullous of the newborn [MIM:131705]
+Epidermolysis bullosa pruriginosa [MIM:604129]
+Toenail dystrophy, isolated [MIM:607523]
+EBD inversa [MIM:226600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL8A2">
+ <field name="name">COL8A2</field>
+ <field name="long_name">collagen, type VIII, alpha 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34.3-p32.3</field>
+ <field name="info">
+Fuchs endothelial corneal dystrophy [MIM:136800]
+Corneal dystrophy, polymorphous posterior, 2 [MIM:122000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL9A1">
+ <field name="name">COL9A1</field>
+ <field name="long_name">collagen, type IX, alpha 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q13</field>
+ <field name="info">
+Epiphyseal dysplasia, multiple, 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL9A2">
+ <field name="name">COL9A2</field>
+ <field name="long_name">collagen, type IX, alpha 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p33-p32.2</field>
+ <field name="info">
+Epiphyseal dysplasia, multiple, 2 [MIM:600204]
+Intervertebral disc disease, susceptibility to [MIM:603932]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COL9A3">
+ <field name="name">COL9A3</field>
+ <field name="long_name">collagen, type IX, alpha 3</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.3</field>
+ <field name="info">
+Epiphyseal dysplasia, multiple, 3 [MIM:600969]
+Epiphyseal dysplasia, multiple, with myopathy
+Intervertebral disc disease, susceptibility to [MIM:603932]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COLQ">
+ <field name="name">COLQ</field>
+ <field name="long_name">collagen-like tail subunit (single strand of homotrimer) of asymmetric acetylcholinesterase</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25</field>
+ <field name="info">
+Endplate acetylcholinesterase deficiency [MIM:603034]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COMA">
+ <field name="name">COMA</field>
+ <field name="long_name">Cogan-type congential oculomotor apraxia</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q13</field>
+ <field name="info">
+Oculomotor apraxia, congential, Cogan-type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COMP">
+ <field name="name">COMP</field>
+ <field name="long_name">cartilage oligomeric matrix protein</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.1</field>
+ <field name="info">
+Pseudoachondroplasia [MIM:177170]
+Epiphyseal dysplasia, multiple 1 [MIM:132400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COMT">
+ <field name="name">COMT</field>
+ <field name="long_name">catechol-O-methyltransferase</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+Schizophrenia, susceptibility to [MIM:181500]
+Panic disorder, susceptibility to [MIM:167870]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COPD">
+ <field name="name">COPD</field>
+ <field name="long_name">Pulmonary disease, chronic obstructive, severe early-onset</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q</field>
+ <field name="info">
+Pulmonary disease, chronic obstructive, severe early-onset</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COQ2">
+ <field name="name">COQ2</field>
+ <field name="long_name">coenzyme Q2 homolog, prenyltransferase (yeast)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21-q22</field>
+ <field name="info">
+Coenzyme Q10 deficiency [MIM:607426]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CORD1">
+ <field name="name">CORD1</field>
+ <field name="long_name">cone rod dystrophy 1 (autosomal dominant)</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.1-q21.3</field>
+ <field name="info">
+Cone-rod retinal dystrophy-1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CORD8">
+ <field name="name">CORD8</field>
+ <field name="long_name">cone rod dystrophy 8</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q12-q24</field>
+ <field name="info">
+Cone-rod dystrophy 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CORS2">
+ <field name="name">CORS2</field>
+ <field name="long_name">cerebello-oculo-renal syndrome 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p12-q13.3</field>
+ <field name="info">
+Cerebellooculorenal syndrome 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COX10">
+ <field name="name">COX10</field>
+ <field name="long_name">COX10 homolog, cytochrome c oxidase assembly protein, heme A: farnesyltransferase (yeast)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p12-p11.2</field>
+ <field name="info">
+Encephalopathy, progressive mitochondrial, with proximal renal tubulopathy due to cytochrome c oxidase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COX15">
+ <field name="name">COX15</field>
+ <field name="long_name">COX15 homolog, cytochrome c oxidase assembly protein (yeast)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+Cardiomyopathy, hypertrophic, early-onset fatal
+Leigh syndrome due to cytochrome c oxidase deficiency [MIM:256000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COX4I2">
+ <field name="name">COX4I2</field>
+ <field name="long_name">cytochrome c oxidase subunit IV isoform 2 (lung)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11.21</field>
+ <field name="info">
+Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis [MIM:612714]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="COX6B1">
+ <field name="name">COX6B1</field>
+ <field name="long_name">cytochrome c oxidase subunit Vib polypeptide 1 (ubiquitous)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+Cytochrome c oxidase deficiency [MIM:220110]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CPA4">
+ <field name="name">CPA4</field>
+ <field name="long_name">carboxypeptidase A4</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CPB2">
+ <field name="name">CPB2</field>
+ <field name="long_name">carboxypeptidase B2 (plasma)</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14.11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CPE">
+ <field name="name">CPE</field>
+ <field name="long_name">carboxypeptidase E</field>
+ <field name="chromosome">4</field>
+ <field name="location">4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CPN1">
+ <field name="name">CPN1</field>
+ <field name="long_name">carboxypeptidase N, polypeptide 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24.2</field>
+ <field name="info">
+Carboxypeptidase N deficiency [MIM:212070]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CPOX">
+ <field name="name">CPOX</field>
+ <field name="long_name">coproporphyrinogen oxidase</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q12</field>
+ <field name="info">
+Coproporphyria [MIM:121300]
+Harderoporphyria [MIM:121300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CPP">
+ <field name="name">CPP</field>
+ <field name="long_name">ceruloplasmin (ferroxidase) pseudogene</field>
+ <field name="chromosome">1</field>
+ <field name="location">1pter-p36.1</field>
+ <field name="info">
+Cataract, posterior polar</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CPROTQ">
+ <field name="name">CPROTQ</field>
+ <field name="long_name">C-reactive protein QTL</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23-q24</field>
+ <field name="info">
+C-reactive protein QTL</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CPS1">
+ <field name="name">CPS1</field>
+ <field name="long_name">carbamoyl-phosphate synthetase 1, mitochondrial</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35</field>
+ <field name="info">
+Carbamoylphosphate synthetase I deficiency [MIM:237300]
+Pulmonary hypertension, familial persistent, of the newborn [MIM:265380]
+Venoocclusive disease after bone marrow transplantation (3) 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CPT1A">
+ <field name="name">CPT1A</field>
+ <field name="long_name">carnitine palmitoyltransferase 1A (liver)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+CPT deficiency, hepatic, type IA [MIM:255120]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CPT1B">
+ <field name="name">CPT1B</field>
+ <field name="long_name">carnitine palmitoyltransferase 1B (muscle)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CPT2">
+ <field name="name">CPT2</field>
+ <field name="long_name">carnitine palmitoyltransferase 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+Myopathy due to CPT II deficiency [MIM:255110]
+CPT deficiency, hepatic, type II [MIM:600649]
+CPT II deficiency, lethal neonatal [MIM:608836]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CPX">
+ <field name="name">CPX</field>
+ <field name="long_name">cleft palate and/or ankyloglossia</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq12-q21</field>
+ <field name="info">
+Cleft palate with ankyloglossia [MIM:303400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CP">
+ <field name="name">CP</field>
+ <field name="long_name">ceruloplasmin (ferroxidase)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q23-q24</field>
+ <field name="info">
+Hypoceruloplasminemia, hereditary [MIM:604290]
+Cerebellar ataxia [MIM:604290]
+Hemosiderosis, systemic, due to aceruloplasminemia [MIM:604290]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CR1">
+ <field name="name">CR1</field>
+ <field name="long_name">complement component (3b/4b) receptor 1 (Knops blood group)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+CR1 deficiency
+?SLE susceptibility
+Blood group, Knops system [MIM:607486]
+Malaria, severe, resistance to [MIM:611162]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CR2">
+ <field name="name">CR2</field>
+ <field name="long_name">complement component (3d/Epstein Barr virus) receptor 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+Systemic lupus erythematosus, susceptibility to, 9 [MIM:610927]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRAC1">
+ <field name="name">CRAC1</field>
+ <field name="long_name">colorectal adenoma and carcinoma 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15.3-q22.1</field>
+ <field name="info">
+Polyposis syndrome, mixed hereditary 1
+Colorectal cancer, susceptibility to, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRAT">
+ <field name="name">CRAT</field>
+ <field name="long_name">carnitine acetyltransferase</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.1</field>
+ <field name="info">
+Carnitine acetyltransferase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRB1">
+ <field name="name">CRB1</field>
+ <field name="long_name">crumbs homolog 1 (Drosophila)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31-q32.1</field>
+ <field name="info">
+Retinitis pigmentosa-12, autosomal recessive [MIM:600105]
+Leber congenital amaurosis 8
+Pigmented paravenous chorioretinal atrophy [MIM:172870]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRBN">
+ <field name="name">CRBN</field>
+ <field name="long_name">cereblon</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26.2</field>
+ <field name="info">
+Mental retardation, autosomal recessive 2A [MIM:607417]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRCL">
+ <field name="name">CRCL</field>
+ <field name="long_name">Creatinine clearance QTL</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p</field>
+ <field name="info">
+Creatinine clearance QTL</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRCS10">
+ <field name="name">CRCS10</field>
+ <field name="long_name">Colorectal cancer, susceptibility to, 10</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+Colorectal cancer, susceptibility to, 10</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRCS11">
+ <field name="name">CRCS11</field>
+ <field name="long_name">Colorectal cancer, susceptibility to, 11</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p12.3</field>
+ <field name="info">
+Colorectal cancer, susceptibility to, 11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRCS2">
+ <field name="name">CRCS2</field>
+ <field name="long_name">Colorectal cancer, susceptibility to, 2</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24</field>
+ <field name="info">
+Colorectal cancer, susceptibility to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRCS5">
+ <field name="name">CRCS5</field>
+ <field name="long_name">Colorectal cancer, susceptibility to, 5</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p14</field>
+ <field name="info">
+Colorectal cancer, susceptibility to, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRCS6">
+ <field name="name">CRCS6</field>
+ <field name="long_name">colorectal cancer, susceptibility to, 6</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q23</field>
+ <field name="info">
+Colorectal cancer, susceptibility to, 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRCS7">
+ <field name="name">CRCS7</field>
+ <field name="long_name">colorectal cancer, susceptibility to, 7</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Colorectal cancer, susceptibility to, 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRCS8">
+ <field name="name">CRCS8</field>
+ <field name="long_name">Colorectal cancer, susceptibility to, 8</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q22.2</field>
+ <field name="info">
+Colorectal cancer, susceptibility to, 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRCS9">
+ <field name="name">CRCS9</field>
+ <field name="long_name">Colorectal cancer, susceptibility to</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22.32-q31.1</field>
+ <field name="info">
+Colorectal cancer, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CREB1">
+ <field name="name">CREB1</field>
+ <field name="long_name">cAMP responsive element binding protein 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q32.3-q34</field>
+ <field name="info">
+Histiocytoma, angiomatoid fibrous, somatic [MIM:612160]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CREBBP">
+ <field name="name">CREBBP</field>
+ <field name="long_name">CREB binding protein</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+Rubenstein-Taybi syndrome [MIM:180849]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRELD1">
+ <field name="name">CRELD1</field>
+ <field name="long_name">cysteine-rich with EGF-like domains 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25.3</field>
+ <field name="info">
+Atrioventricular septal defect, susceptibility to, 2 [MIM:606217]
+Atrioventricular septal defect, partial, with heterotaxy syndrome [MIM:606217]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRHR1">
+ <field name="name">CRHR1</field>
+ <field name="long_name">corticotropin releasing hormone receptor 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRH">
+ <field name="name">CRH</field>
+ <field name="long_name">corticotropin releasing hormone</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q13</field>
+ <field name="info">
+ACTH deficiency [MIM:201400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRISP2">
+ <field name="name">CRISP2</field>
+ <field name="long_name">cysteine-rich secretory protein 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRLF1">
+ <field name="name">CRLF1</field>
+ <field name="long_name">cytokine receptor-like factor 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p12</field>
+ <field name="info">
+Cold-induced sweating syndrome [MIM:272430]
+Crisponi syndrome [MIM:601378]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRP">
+ <field name="name">CRP</field>
+ <field name="long_name">C-reactive protein, pentraxin-related</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21-q23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRSA">
+ <field name="name">CRSA</field>
+ <field name="long_name">Craniosynostosis, Adelaide type</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16</field>
+ <field name="info">
+Craniosynostosis, Adelaide type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRS">
+ <field name="name">CRS</field>
+ <field name="long_name">craniosynostosis</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p21.3-p21.2</field>
+ <field name="info">
+Craniosynostosis, type 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRTAP">
+ <field name="name">CRTAP</field>
+ <field name="long_name">cartilage associated protein</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p22</field>
+ <field name="info">
+Osteogenesis imperfecta, type IIB [MIM:610854]
+Osteogenesis imperfecta, type VII [MIM:610682]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRTC1">
+ <field name="name">CRTC1</field>
+ <field name="long_name">CREB regulated transcription coactivator 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13</field>
+ <field name="info">
+Mucoepidermoid salivary gland carcinoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRX">
+ <field name="name">CRX</field>
+ <field name="long_name">cone-rod homeobox</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+Cone-rod retinal dystrophy-2 [MIM:120970]
+Leber congenital amaurosis 7
+Retinitis pigmentosa, late-onset dominant [MIM:268000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRYAA">
+ <field name="name">CRYAA</field>
+ <field name="long_name">crystallin, alpha A</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Cataract, zonular central nuclear, autosomal dominant
+Cataract, congenital, autosomal recessive
+Cataract, autosomal dominant nuclear</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRYAB">
+ <field name="name">CRYAB</field>
+ <field name="long_name">crystallin, alpha B</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22.3-q23.1</field>
+ <field name="info">
+Myopathy, cardioskeletal, desmin-related, with cataract [MIM:608810]
+Cataract, posterior polar 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRYBA1">
+ <field name="name">CRYBA1</field>
+ <field name="long_name">crystallin, beta A1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.1-q12</field>
+ <field name="info">
+Cataract, congenital zonular, with sutural opacities [MIM:600881]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRYBA4">
+ <field name="name">CRYBA4</field>
+ <field name="long_name">crystallin, beta A4</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2-q13.1</field>
+ <field name="info">
+Cataract, lamellar 2 [MIM:610425]
+Microphthalmia, isolated, with cataract 4 [MIM:610426]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRYBB1">
+ <field name="name">CRYBB1</field>
+ <field name="long_name">crystallin, beta B1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2-q12.1</field>
+ <field name="info">
+Cataract, pulverulent
+Cataract, congenital nuclear, autosomal recessive 3 [MIM:611544]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRYBB2">
+ <field name="name">CRYBB2</field>
+ <field name="long_name">crystallin, beta B2</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2-q12.2</field>
+ <field name="info">
+Cataract, cerulean, type 2 [MIM:601547]
+Cataract, sutural, with punctate and cerulean opacities [MIM:607133]
+Cataract, Coppock-like [MIM:604307]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRYBB3">
+ <field name="name">CRYBB3</field>
+ <field name="long_name">crystallin, beta B3</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2-q12.2</field>
+ <field name="info">
+Cataract, congenital nuclear, 2 [MIM:609741]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRYGC">
+ <field name="name">CRYGC</field>
+ <field name="long_name">crystallin, gamma C</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33-q35</field>
+ <field name="info">
+Cataract, Coppock-like [MIM:604307]
+Cataract, variable zonular pulverulent</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRYGD">
+ <field name="name">CRYGD</field>
+ <field name="long_name">crystallin, gamma D</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33-q35</field>
+ <field name="info">
+Cataracts, punctate, progressive juvenile-onset
+Cataract, crystalline aculeiform [MIM:115700]
+Cataract, congenital, cerulean type, 3 [MIM:608983]
+Cataract, nonnuclear polymorphic congenital [MIM:601286]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRYGS">
+ <field name="name">CRYGS</field>
+ <field name="long_name">crystallin, gamma S</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27</field>
+ <field name="info">
+Cataract, progressive polymorphic cortical</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CRYM">
+ <field name="name">CRYM</field>
+ <field name="long_name">crystallin, mu</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.11-p12.3</field>
+ <field name="info">
+Deafness, autosomal dominant 40</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CSE">
+ <field name="name">CSE</field>
+ <field name="long_name">choreoathetosis/spasticity, episodic (paroxysmal choreoathetosis/spasticity)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p</field>
+ <field name="info">
+Choreoathetosis/spasticity, episodic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CSF1R">
+ <field name="name">CSF1R</field>
+ <field name="long_name">colony stimulating factor 1 receptor</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q33.2-q33.3</field>
+ <field name="info">
+Myeloid malignancy, predisposition to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CSF1">
+ <field name="name">CSF1</field>
+ <field name="long_name">colony stimulating factor 1 (macrophage)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p21-p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CSF2RA">
+ <field name="name">CSF2RA</field>
+ <field name="long_name">colony stimulating factor 2 receptor, alpha, low-affinity (granulocyte-macrophage)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.32</field>
+ <field name="info">
+Pulmonary alveolar proteinosis [MIM:300770]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CSF2RB">
+ <field name="name">CSF2RB</field>
+ <field name="long_name">colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.2-q13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CSF2">
+ <field name="name">CSF2</field>
+ <field name="long_name">colony stimulating factor 2 (granulocyte-macrophage)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CSF3R">
+ <field name="name">CSF3R</field>
+ <field name="long_name">colony stimulating factor 3 receptor (granulocyte)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p35-p34.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CSH1">
+ <field name="name">CSH1</field>
+ <field name="long_name">chorionic somatomammotropin hormone 1 (placental lactogen)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q22-q24</field>
+ <field name="info">
+Placental lactogen deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CSNK1D">
+ <field name="name">CSNK1D</field>
+ <field name="long_name">casein kinase 1, delta</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CSNK1E">
+ <field name="name">CSNK1E</field>
+ <field name="long_name">casein kinase 1, epsilon</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12-q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CSRP3">
+ <field name="name">CSRP3</field>
+ <field name="long_name">cysteine and glycine-rich protein 3 (cardiac LIM protein)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.1</field>
+ <field name="info">
+Cardiomyopathy, dilated, 1M [MIM:607482]
+Cardiomyopathy, familial hypertrophic, 12 [MIM:612124]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CST3">
+ <field name="name">CST3</field>
+ <field name="long_name">cystatin C</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p11.2</field>
+ <field name="info">
+Cerebral amyloid angiopathy [MIM:105150]
+Macular degeneration, age-related, 11 [MIM:611953]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CSTA">
+ <field name="name">CSTA</field>
+ <field name="long_name">cystatin A (stefin A)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CSTB">
+ <field name="name">CSTB</field>
+ <field name="long_name">cystatin B (stefin B)</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Epilepsy, progressive myoclonic 1 [MIM:254800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CS">
+ <field name="name">CS</field>
+ <field name="long_name">citrate synthase</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p11-qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTAA1">
+ <field name="name">CTAA1</field>
+ <field name="long_name">cataract, anterior polar 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24-qter</field>
+ <field name="info">
+Cataract, anterior polar-1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTAA2">
+ <field name="name">CTAA2</field>
+ <field name="long_name">cataract, anterior polar 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13</field>
+ <field name="info">
+Cataract, anterior polar-2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTDP1">
+ <field name="name">CTDP1</field>
+ <field name="long_name">CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q23</field>
+ <field name="info">
+Congenital cataracts, facial dysmorphism, and neuropathy [MIM:604168]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTF1">
+ <field name="name">CTF1</field>
+ <field name="long_name">cardiotrophin 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p11.2-p11.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTGF">
+ <field name="name">CTGF</field>
+ <field name="long_name">connective tissue growth factor</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTHM">
+ <field name="name">CTHM</field>
+ <field name="long_name">cono-truncal heart malformation</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+Conotruncal anomaly face syndrome [MIM:217095]
+DiGeorge syndrome [MIM:188400]
+Velocardiofacial syndrome [MIM:192430]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTH">
+ <field name="name">CTH</field>
+ <field name="long_name">cystathionase (cystathionine gamma-lyase)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31.1</field>
+ <field name="info">
+Cystathioninuria [MIM:219500]
+Homocysteine, total plasma, elevated</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTLA4">
+ <field name="name">CTLA4</field>
+ <field name="long_name">cytotoxic T-lymphocyte-associated protein 4</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33</field>
+ <field name="info">
+Graves disease, susceptibility to [MIM:275000]
+Hypothyroidism, autoimmune [MIM:140300]
+Diabetes mellitus, insulin-dependent, susceptibility to [MIM:601388]
+Celiac disease, susceptibility to [MIM:609755]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTNNA3">
+ <field name="name">CTNNA3</field>
+ <field name="long_name">catenin (cadherin-associated protein), alpha 3</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTNNB1">
+ <field name="name">CTNNB1</field>
+ <field name="long_name">catenin (cadherin-associated protein), beta 1, 88kDa</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p22-p21.3</field>
+ <field name="info">
+Colorectal cancer
+Hepatoblastoma
+Pilomatricoma [MIM:132600]
+Ovarian cancer [MIM:167000]
+Hepatocellular carcinoma [MIM:114550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTNND2">
+ <field name="name">CTNND2</field>
+ <field name="long_name">catenin (cadherin-associated protein), delta 2 (neural plakophilin-related arm-repeat protein)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.2</field>
+ <field name="info">
+Mental retardation in cri-du-chat syndrome [MIM:123450]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTNS">
+ <field name="name">CTNS</field>
+ <field name="long_name">cystinosis, nephropathic</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13</field>
+ <field name="info">
+Cystinosis, nephropathic [MIM:219800]
+Cystinosis, ocular nonnephropathic [MIM:219750]
+Cystinosis, late-onset juvenile or adolescent nephropathic [MIM:219900]
+Cystinosis, atypical nephropathic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTPP5">
+ <field name="name">CTPP5</field>
+ <field name="long_name">Cataract, posterior polar, 5</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q22-q23</field>
+ <field name="info">
+Cataract, posterior polar, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTPP">
+ <field name="name">CTPP</field>
+ <field name="long_name">Cataract, posterior polar</field>
+ <field name="chromosome">1</field>
+ <field name="location">1pter-p36.1</field>
+ <field name="info">
+Cataract, posterior polar</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTRC">
+ <field name="name">CTRC</field>
+ <field name="long_name">chymotrypsin C (caldecrin)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.21</field>
+ <field name="info">
+Pancreatitis, chronic, susceptibilty to [MIM:167800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTSA">
+ <field name="name">CTSA</field>
+ <field name="long_name">cathepsin A</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.1</field>
+ <field name="info">
+Galactosialidosis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTSB">
+ <field name="name">CTSB</field>
+ <field name="long_name">cathepsin B</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTSC">
+ <field name="name">CTSC</field>
+ <field name="long_name">cathepsin C</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q14.1-q14.3</field>
+ <field name="info">
+Papillon-Lefevre syndrome [MIM:245000]
+Haim-Munk syndrome [MIM:245010]
+Periodontitis, juvenile [MIM:170650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTSD">
+ <field name="name">CTSD</field>
+ <field name="long_name">cathepsin D</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Ceroid lipofuscinosis, neuronal, 10 [MIM:610127]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTSG">
+ <field name="name">CTSG</field>
+ <field name="long_name">cathepsin G</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CTSK">
+ <field name="name">CTSK</field>
+ <field name="long_name">cathepsin K</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Pycnodysostosis [MIM:265800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CUBN">
+ <field name="name">CUBN</field>
+ <field name="long_name">cubilin (intrinsic factor-cobalamin receptor)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p12.1</field>
+ <field name="info">
+Megaloblastic anemia-1, Finnish type [MIM:261100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CUL4B">
+ <field name="name">CUL4B</field>
+ <field name="long_name">cullin 4B</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq23</field>
+ <field name="info">
+Mental retardation syndrome, X-linked, Cabezas type [MIM:300354]
+Mental retardation-hypotonic facies syndrome, X-linked, 2 [MIM:300639]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CUL7">
+ <field name="name">CUL7</field>
+ <field name="long_name">cullin 7</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.1</field>
+ <field name="info">
+3-M syndrome [MIM:273750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CVD1">
+ <field name="name">CVD1</field>
+ <field name="long_name">cardiac valvular dysplasia-1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Cardiac valvular dysplasia-1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CVMRF">
+ <field name="name">CVMRF</field>
+ <field name="long_name">cubitus valgus with mental retardation and unusual facies</field>
+ <field name="chromosome">X</field>
+ <field name="location">X</field>
+ <field name="info">
+Cubitus valgus with mental retardation and unusual facies</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CX3CR1">
+ <field name="name">CX3CR1</field>
+ <field name="long_name">chemokine (C-X3-C motif) receptor 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3pter-p21</field>
+ <field name="info">
+Rapid progression to AIDS from HIV1 infection [MIM:609423]
+Coronary artery disease, resistance to [MIM:607339]
+Macular degeneration, age-related, susceptibility to [MIM:603075]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CXCL10">
+ <field name="name">CXCL10</field>
+ <field name="long_name">chemokine (C-X-C motif) ligand 10</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CXCL11">
+ <field name="name">CXCL11</field>
+ <field name="long_name">chemokine (C-X-C motif) ligand 11</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CXCL12">
+ <field name="name">CXCL12</field>
+ <field name="long_name">chemokine (C-X-C motif) ligand 12 (stromal cell-derived factor 1)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q11.1</field>
+ <field name="info">
+AIDS, resistance to [MIM:609423]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CXCL16">
+ <field name="name">CXCL16</field>
+ <field name="long_name">chemokine (C-X-C motif) ligand 16</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CXCR4">
+ <field name="name">CXCR4</field>
+ <field name="long_name">chemokine (C-X-C motif) receptor 4</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q21</field>
+ <field name="info">
+WHIM syndrome [MIM:193670]
+Myelokathexis, isolated</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYB5A">
+ <field name="name">CYB5A</field>
+ <field name="long_name">cytochrome b5 type A (microsomal)</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q23</field>
+ <field name="info">
+Methemoglobinemia due to cytochrome b5 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYB5R3">
+ <field name="name">CYB5R3</field>
+ <field name="long_name">cytochrome b5 reductase 3</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.31-qter</field>
+ <field name="info">
+Methemoglobinemia, type I
+Methemoglobinemia, type II</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYBA">
+ <field name="name">CYBA</field>
+ <field name="long_name">cytochrome b-245, alpha polypeptide</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24</field>
+ <field name="info">
+Chronic granulomatous disease, autosomal, due to deficiency of CYBA [MIM:233690]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYBB">
+ <field name="name">CYBB</field>
+ <field name="long_name">cytochrome b-245, beta polypeptide</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp21.1</field>
+ <field name="info">
+Chronic granulomatous disease, X-linked [MIM:306400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYCS">
+ <field name="name">CYCS</field>
+ <field name="long_name">cytochrome c, somatic</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15.2</field>
+ <field name="info">
+Thrombocytopenia 4 [MIM:612004]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP11B1">
+ <field name="name">CYP11B1</field>
+ <field name="long_name">cytochrome P450, family 11, subfamily B, polypeptide 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21</field>
+ <field name="info">
+Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency [MIM:202010]
+Aldosteronism, glucocorticoid-remediable [MIM:103900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP11B2">
+ <field name="name">CYP11B2</field>
+ <field name="long_name">cytochrome P450, family 11, subfamily B, polypeptide 2</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21</field>
+ <field name="info">
+Hypoaldosteronism, congenital, due to CMO II deficiency [MIM:610600]
+Hypoaldosteronism, congenital, due to CMO I deficiency [MIM:203400]
+Low renin hypertension, susceptibility to
+Aldosterone to renin ratio raised</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP17A1">
+ <field name="name">CYP17A1</field>
+ <field name="long_name">cytochrome P450, family 17, subfamily A, polypeptide 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24.3</field>
+ <field name="info">
+17-alpha-hydroxylase/17,20-lyase deficiency [MIM:202110]
+17,20-lyase deficiency, isolated [MIM:202110]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP19A1">
+ <field name="name">CYP19A1</field>
+ <field name="long_name">cytochrome P450, family 19, subfamily A, polypeptide 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21.1</field>
+ <field name="info">
+Aromatase deficiency
+Aromatase excess syndrome [MIM:139300]
+Pseudohermaphroditism, female, due to placental aromatase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP1A1">
+ <field name="name">CYP1A1</field>
+ <field name="long_name">cytochrome P450, family 1, subfamily A, polypeptide 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22-q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP1A2">
+ <field name="name">CYP1A2</field>
+ <field name="long_name">cytochrome P450, family 1, subfamily A, polypeptide 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22-qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP1B1">
+ <field name="name">CYP1B1</field>
+ <field name="long_name">cytochrome P450, family 1, subfamily B, polypeptide 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p22-p21</field>
+ <field name="info">
+Glaucoma 3A, primary congenital [MIM:231300]
+Peters anomaly [MIM:604229]
+Glaucoma, early-onset, digenic
+Glaucoma, primary open angle, adult-onset [MIM:137760]
+Glaucoma, primary open angle, juvenile-onset [MIM:137750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP21A2">
+ <field name="name">CYP21A2</field>
+ <field name="long_name">cytochrome P450, family 21, subfamily A, polypeptide 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
+Hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP26A1">
+ <field name="name">CYP26A1</field>
+ <field name="long_name">cytochrome P450, family 26, subfamily A, polypeptide 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23-q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP27A1">
+ <field name="name">CYP27A1</field>
+ <field name="long_name">cytochrome P450, family 27, subfamily A, polypeptide 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33-qter</field>
+ <field name="info">
+Cerebrotendinous xanthomatosis [MIM:213700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP27B1">
+ <field name="name">CYP27B1</field>
+ <field name="long_name">cytochrome P450, family 27, subfamily B, polypeptide 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13.1-q13.3</field>
+ <field name="info">
+Vitamin D-dependent rickets, type I [MIM:264700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP2A13">
+ <field name="name">CYP2A13</field>
+ <field name="long_name">cytochrome P450, family 2, subfamily A, polypeptide 13</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP2A6">
+ <field name="name">CYP2A6</field>
+ <field name="long_name">cytochrome P450, family 2, subfamily A, polypeptide 6</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+Coumarin resistance [MIM:122700]
+Nicotine addiction, protection from [MIM:188890]
+Lung cancer, resistance to [MIM:211980]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP2B6">
+ <field name="name">CYP2B6</field>
+ <field name="long_name">cytochrome P450, family 2, subfamily B, polypeptide 6</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP2C19">
+ <field name="name">CYP2C19</field>
+ <field name="long_name">cytochrome P450, family 2, subfamily C, polypeptide 19</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24.1-q24.3</field>
+ <field name="info">
+Mephenytoin poor metabolizer [MIM:609535]
+Opremazole poor metagolizer [MIM:609535]
+Proguanil poor metabolizer [MIM:609535]
+Clopidogrel, impaired responsiveness to [MIM:609535]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP2C8">
+ <field name="name">CYP2C8</field>
+ <field name="long_name">cytochrome P450, family 2, subfamily C, polypeptide 8</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23.3</field>
+ <field name="info">
+Rhabdomyolysis, cerivastatin-induced</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP2C9">
+ <field name="name">CYP2C9</field>
+ <field name="long_name">cytochrome P450, family 2, subfamily C, polypeptide 9</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+Tolbutamide poor metabolizer
+Warfarin sensitivity [MIM:122700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP2D6">
+ <field name="name">CYP2D6</field>
+ <field name="long_name">cytochrome P450, family 2, subfamily D, polypeptide 6</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.1</field>
+ <field name="info">
+Debrisoquine sensitivity [MIM:608902]
+Codeine sensitivity [MIM:608902]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP2E1">
+ <field name="name">CYP2E1</field>
+ <field name="long_name">cytochrome P450, family 2, subfamily E, polypeptide 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24.3-qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP2F1">
+ <field name="name">CYP2F1</field>
+ <field name="long_name">cytochrome P450, family 2, subfamily F, polypeptide 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP2J2">
+ <field name="name">CYP2J2</field>
+ <field name="long_name">cytochrome P450, family 2, subfamily J, polypeptide 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31.3-p31.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP2R1">
+ <field name="name">CYP2R1</field>
+ <field name="long_name">cytochrome P450, family 2, subfamily R, polypeptide 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.2</field>
+ <field name="info">
+Rickets due to defect in vitamin D 25-hydroxylation [MIM:600081]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP3A43">
+ <field name="name">CYP3A43</field>
+ <field name="long_name">cytochrome P450, family 3, subfamily A, polypeptide 43</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP3A4">
+ <field name="name">CYP3A4</field>
+ <field name="long_name">cytochrome P450, family 3, subfamily A, polypeptide 4</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP3A5">
+ <field name="name">CYP3A5</field>
+ <field name="long_name">cytochrome P450, family 3, subfamily A, polypeptide 5</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22.1</field>
+ <field name="info">
+Hypertension, salt-sensitive essential, susceptibility to [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP3A7">
+ <field name="name">CYP3A7</field>
+ <field name="long_name">cytochrome P450, family 3, subfamily A, polypeptide 7</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP46A1">
+ <field name="name">CYP46A1</field>
+ <field name="long_name">cytochrome P450, family 46, subfamily A, polypeptide 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP4A11">
+ <field name="name">CYP4A11</field>
+ <field name="long_name">cytochrome P450, family 4, subfamily A, polypeptide 11</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p33</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP4B1">
+ <field name="name">CYP4B1</field>
+ <field name="long_name">cytochrome P450, family 4, subfamily B, polypeptide 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP4F12">
+ <field name="name">CYP4F12</field>
+ <field name="long_name">cytochrome P450, family 4, subfamily F, polypeptide 12</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP4F22">
+ <field name="name">CYP4F22</field>
+ <field name="long_name">cytochrome P450, family 4, subfamily F, polypeptide 22</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.12</field>
+ <field name="info">
+Ichthyosis, lamellar, 3 [MIM:604777]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP4V2">
+ <field name="name">CYP4V2</field>
+ <field name="long_name">cytochrome P450, family 4, subfamily V, polypeptide 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q35.1</field>
+ <field name="info">
+Bietti crystalline corneoretinal dystrophy [MIM:210370]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP7A1">
+ <field name="name">CYP7A1</field>
+ <field name="long_name">cytochrome P450, family 7, subfamily A, polypeptide 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q11-q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYP7B1">
+ <field name="name">CYP7B1</field>
+ <field name="long_name">cytochrome P450, family 7, subfamily B, polypeptide 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21.3</field>
+ <field name="info">
+Bile acid synthesis defect, congenital, 3
+Spastic paraplegia-5A [MIM:270800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYSLTR1">
+ <field name="name">CYSLTR1</field>
+ <field name="long_name">cysteinyl leukotriene receptor 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13-q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="CYSLTR2">
+ <field name="name">CYSLTR2</field>
+ <field name="long_name">cysteinyl leukotriene receptor 2</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="D13S25">
+ <field name="name">D13S25</field>
+ <field name="long_name">Disrupted in B-cell neoplasia</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14</field>
+ <field name="info">
+Leukemia, chronic lymphocytic, susceptibility to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="D2HGDH">
+ <field name="name">D2HGDH</field>
+ <field name="long_name">D-2-hydroxyglutarate dehydrogenase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.3</field>
+ <field name="info">
+D-2-hydroxyglutaric aciduria [MIM:600721]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DAG1">
+ <field name="name">DAG1</field>
+ <field name="long_name">dystroglycan 1 (dystrophin-associated glycoprotein 1)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DAOA">
+ <field name="name">DAOA</field>
+ <field name="long_name">D-amino acid oxidase activator</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q34</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DAO">
+ <field name="name">DAO</field>
+ <field name="long_name">D-amino-acid oxidase</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DAPK1">
+ <field name="name">DAPK1</field>
+ <field name="long_name">death-associated protein kinase 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DARS2">
+ <field name="name">DARS2</field>
+ <field name="long_name">aspartyl-tRNA synthetase 2, mitochondrial</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q25.1</field>
+ <field name="info">
+Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation [MIM:611105]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DAZ2">
+ <field name="name">DAZ2</field>
+ <field name="long_name">deleted in azoospermia 2</field>
+ <field name="chromosome">Y</field>
+ <field name="location">Yq11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DAZL">
+ <field name="name">DAZL</field>
+ <field name="long_name">deleted in azoospermia-like</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p24</field>
+ <field name="info">
+Spermatogenic failure, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DBA2">
+ <field name="name">DBA2</field>
+ <field name="long_name">Diamond-Blackfan anemia 2</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23.3-p22</field>
+ <field name="info">
+Anemia, Diamond-Blackfan [MIM:105650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DBH">
+ <field name="name">DBH</field>
+ <field name="long_name">dopamine beta-hydroxylase (dopamine beta-monooxygenase)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+Dopamine-beta-hydroxylase activity levels, plasma
+Parkinson disease, resistance to [MIM:168600]
+Dopamine beta-hydroxylase deficiency [MIM:223360]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DBQD">
+ <field name="name">DBQD</field>
+ <field name="long_name">Desbuquois syndrome</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25.3</field>
+ <field name="info">
+Desbuquois syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DBT">
+ <field name="name">DBT</field>
+ <field name="long_name">dihydrolipoamide branched chain transacylase E2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+Maple syrup urine disease, type II [MIM:248600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DCC">
+ <field name="name">DCC</field>
+ <field name="long_name">deleted in colorectal carcinoma</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.3</field>
+ <field name="info">
+Colorectal cancer</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DCK">
+ <field name="name">DCK</field>
+ <field name="long_name">deoxycytidine kinase</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q13.3-q21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DCLRE1C">
+ <field name="name">DCLRE1C</field>
+ <field name="long_name">DNA cross-link repair 1C (PSO2 homolog, S. cerevisiae)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p</field>
+ <field name="info">
+Severe combined immunodeficiency, Athabascan type [MIM:602450]
+Omenn syndrome [MIM:603554]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DCN">
+ <field name="name">DCN</field>
+ <field name="long_name">decorin</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q21.3</field>
+ <field name="info">
+Corneal dystrophy, congenital stromal [MIM:610048]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DCR">
+ <field name="name">DCR</field>
+ <field name="long_name">Down syndrome chromosome region</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Down syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DCTN1">
+ <field name="name">DCTN1</field>
+ <field name="long_name">dynactin 1 (p150, glued homolog, Drosophila)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p13</field>
+ <field name="info">
+Neuropathy, distal hereditary motor, type VIIB [MIM:607641]
+Amyotrophic lateral sclerosis, susceptibility to [MIM:105400]
+Perry syndrome [MIM:168605]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DCX">
+ <field name="name">DCX</field>
+ <field name="long_name">doublecortin</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22.3-q23</field>
+ <field name="info">
+Lissencephaly, X-linked [MIM:300067]
+Subcortical laminal heteropia, X-linked [MIM:300067]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DDAH2">
+ <field name="name">DDAH2</field>
+ <field name="long_name">dimethylarginine dimethylaminohydrolase 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DDB1">
+ <field name="name">DDB1</field>
+ <field name="long_name">damage-specific DNA binding protein 1, 127kDa</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q12-q13</field>
+ <field name="info">
+Xeroderma pigmentosum, group E, subtype 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DDB2">
+ <field name="name">DDB2</field>
+ <field name="long_name">damage-specific DNA binding protein 2, 48kDa</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p12-p11</field>
+ <field name="info">
+Xeroderma pigmentosum, group E, DDB-negative subtype [MIM:278740]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DDC">
+ <field name="name">DDC</field>
+ <field name="long_name">dopa decarboxylase (aromatic L-amino acid decarboxylase)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p11</field>
+ <field name="info">
+Aromatic L-amino acid decarboxylase deficiency [MIM:608643]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DDIT3">
+ <field name="name">DDIT3</field>
+ <field name="long_name">DNA-damage-inducible transcript 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13.1-q13.2</field>
+ <field name="info">
+Myxoid liposarcoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DDX20">
+ <field name="name">DDX20</field>
+ <field name="long_name">DEAD (Asp-Glu-Ala-Asp) box polypeptide 20</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p21.1-p13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DDX3Y">
+ <field name="name">DDX3Y</field>
+ <field name="long_name">DEAD (Asp-Glu-Ala-Asp) box polypeptide 3, Y-linked</field>
+ <field name="chromosome">Y</field>
+ <field name="location">Yq11</field>
+ <field name="info">
+Y Chromosome Infertility</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DDX5">
+ <field name="name">DDX5</field>
+ <field name="long_name">DEAD (Asp-Glu-Ala-Asp) box polypeptide 5</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23-q25</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DEC1">
+ <field name="name">DEC1</field>
+ <field name="long_name">deleted in esophageal cancer 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q32</field>
+ <field name="info">
+Esophageal squamous cell carcinoma [MIM:133239]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DECR1">
+ <field name="name">DECR1</field>
+ <field name="long_name">2,4-dienoyl CoA reductase 1, mitochondrial</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21.3</field>
+ <field name="info">
+DECR deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DEC">
+ <field name="name">DEC</field>
+ <field name="long_name">Deleted in endometrial carcinoma</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q26</field>
+ <field name="info">
+Endometrial carcinoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DEFB1">
+ <field name="name">DEFB1</field>
+ <field name="long_name">defensin, beta 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DEFB4">
+ <field name="name">DEFB4</field>
+ <field name="long_name">defensin, beta 4</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23.1</field>
+ <field name="info">
+Crohn disease, susceptibility to [MIM:266600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DEK">
+ <field name="name">DEK</field>
+ <field name="long_name">DEK oncogene</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p23</field>
+ <field name="info">
+Leukemia, acute nonlymphocytic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DES">
+ <field name="name">DES</field>
+ <field name="long_name">desmin</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35</field>
+ <field name="info">
+Myopathy, desmin-related, cardioskeletal [MIM:601419]
+Cardiomyopathy, dilated, 1I [MIM:604765]
+Scapuloperoneal syndrome, neurogenic, Kaeser type [MIM:181400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFCTRPS">
+ <field name="name">DFCTRPS</field>
+ <field name="long_name">Deafness, cataract, retinitis pigmentosa, and sperm abnormalities</field>
+ <field name="chromosome">X</field>
+ <field name="location">X</field>
+ <field name="info">
+Deafness, cataract, retinitis pigmentosa, and sperm abnormalities</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFN2">
+ <field name="name">DFN2</field>
+ <field name="long_name">deafness, X-linked 2, perceptive, congenital</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22</field>
+ <field name="info">
+Deafness, X-linked 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFN4">
+ <field name="name">DFN4</field>
+ <field name="long_name">deafness, X-linked 4, congenital sensorineural</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp21.2</field>
+ <field name="info">
+Deafness, X-linked 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFN6">
+ <field name="name">DFN6</field>
+ <field name="long_name">deafness, X-linked 6, sensorineural</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22</field>
+ <field name="info">
+Deafness, X-linked 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA16">
+ <field name="name">DFNA16</field>
+ <field name="long_name">deafness, autosomal dominant 16</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q23-q24.3</field>
+ <field name="info">
+Deafness, autosomal dominant 16</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA18">
+ <field name="name">DFNA18</field>
+ <field name="long_name">deafness, autosomal dominant 18</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q22</field>
+ <field name="info">
+Deafness, autosomal dominant 18</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA21">
+ <field name="name">DFNA21</field>
+ <field name="long_name">deafness, autosomal dominant 21</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Deafness, autosomal dominant 21</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA24">
+ <field name="name">DFNA24</field>
+ <field name="long_name">deafness, autosomal dominant 24</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q35-qter</field>
+ <field name="info">
+Deafness, autosomal dominant 24</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA27">
+ <field name="name">DFNA27</field>
+ <field name="long_name">deafness, autosomal dominant 27</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q12-q13.1</field>
+ <field name="info">
+Deafness, autosomal dominant 27</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA30">
+ <field name="name">DFNA30</field>
+ <field name="long_name">deafness, autosomal dominant 30</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q25-q26</field>
+ <field name="info">
+Deafness, autosomal dominant 30</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA31">
+ <field name="name">DFNA31</field>
+ <field name="long_name">deafness, autosomal dominant 31</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Deafness, autosomal dominant 31</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA40">
+ <field name="name">DFNA40</field>
+ <field name="long_name">deafness, autosomal dominant 40</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.11-p12.3</field>
+ <field name="info">
+Deafness, autosomal dominant 40</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA41">
+ <field name="name">DFNA41</field>
+ <field name="long_name">deafness, autosomal dominant 41</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.32-qter</field>
+ <field name="info">
+Deafness, autosomal dominant 41</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA49">
+ <field name="name">DFNA49</field>
+ <field name="long_name">deafness, autosomal dominant 49</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21-q23</field>
+ <field name="info">
+Deafness, autosomal dominant 49</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA52">
+ <field name="name">DFNA52</field>
+ <field name="long_name">deafness, autosomal dominant 52</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q28</field>
+ <field name="info">
+Deafness, autosomal dominant 52</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA53">
+ <field name="name">DFNA53</field>
+ <field name="long_name">deafness, autosomal dominant 53</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2-q12</field>
+ <field name="info">
+Deafness, autosomal dominant 53</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA59">
+ <field name="name">DFNA59</field>
+ <field name="long_name">deafness, autosomal dominant 59</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p14.2-q12.3</field>
+ <field name="info">
+Deafness, autosomal dominant 59</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA5">
+ <field name="name">DFNA5</field>
+ <field name="long_name">deafness, autosomal dominant 5</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15</field>
+ <field name="info">
+Deafness, autosomal dominant 5 [MIM:600994]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNA7">
+ <field name="name">DFNA7</field>
+ <field name="long_name">deafness, autosomal dominant 7</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21-q23</field>
+ <field name="info">
+Deafness, autosomal dominant 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB13">
+ <field name="name">DFNB13</field>
+ <field name="long_name">deafness, autosomal recessive 13</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q34-q36</field>
+ <field name="info">
+Deafness, autosomal recessive 13</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB14">
+ <field name="name">DFNB14</field>
+ <field name="long_name">deafness, autosomal recessive 14</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31</field>
+ <field name="info">
+Deafness, autosomal recessive 14</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB15">
+ <field name="name">DFNB15</field>
+ <field name="long_name">deafness, autosomal recessive 15</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q</field>
+ <field name="info">
+Deafness, autosomal recessive 15</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB17">
+ <field name="name">DFNB17</field>
+ <field name="long_name">deafness, autosomal recessive 17</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31</field>
+ <field name="info">
+Deafness, autosomal recessive 17</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB20">
+ <field name="name">DFNB20</field>
+ <field name="long_name">deafness, autosomal recessive 20</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q25-qter</field>
+ <field name="info">
+Deafness, autosomal recessive 20</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB26">
+ <field name="name">DFNB26</field>
+ <field name="long_name">deafness, autosomal recessive 26</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q31</field>
+ <field name="info">
+Deafness, autosomal recessive 26</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB27">
+ <field name="name">DFNB27</field>
+ <field name="long_name">deafness, autosomal recessive 27</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q23-q31</field>
+ <field name="info">
+Deafness, autosomal recessive 27</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB31">
+ <field name="name">DFNB31</field>
+ <field name="long_name">deafness, autosomal recessive 31</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q32-q34</field>
+ <field name="info">
+Deafness, autosomal recessive 31 [MIM:607084]
+Usher syndrome, type IID [MIM:611383]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB33">
+ <field name="name">DFNB33</field>
+ <field name="long_name">deafness, autosomal recessive 33</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p11.23-q21.1</field>
+ <field name="info">
+Deafness, autosomal recessive 33</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB38">
+ <field name="name">DFNB38</field>
+ <field name="long_name">deafness, autosomal recessive 38</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q26-q27</field>
+ <field name="info">
+Deafness, autosomal recessive 38</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB39">
+ <field name="name">DFNB39</field>
+ <field name="long_name">deafness, autosomal recessive 39</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.22-q21.12</field>
+ <field name="info">
+Deafness, autosomal recessive 39</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB40">
+ <field name="name">DFNB40</field>
+ <field name="long_name">deafness, autosomal recessive 40</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.21-q12.1</field>
+ <field name="info">
+Deafness, autosomal recessive 40</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB44">
+ <field name="name">DFNB44</field>
+ <field name="long_name">deafness, autosomal recessive 44</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14.1-q11.22</field>
+ <field name="info">
+Deafness, autosomal recessive 44</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB45">
+ <field name="name">DFNB45</field>
+ <field name="long_name">deafness, autosomal recessive 45</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q43-q44</field>
+ <field name="info">
+Deafness, autosomal recessive 45</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB46">
+ <field name="name">DFNB46</field>
+ <field name="long_name">deafness, autosomal recessive 46</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.32-p11.31</field>
+ <field name="info">
+Deafness, neurosensory, autosomal recessive 46</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB47">
+ <field name="name">DFNB47</field>
+ <field name="long_name">deafness, autosomal recessive 47</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p25.1-p24.3</field>
+ <field name="info">
+Deafness, neurosensory, autosomal recessive 47</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB51">
+ <field name="name">DFNB51</field>
+ <field name="long_name">deafness, autosomal recessive 51</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13-p12</field>
+ <field name="info">
+Deafness, autosomal recessive 51</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB55">
+ <field name="name">DFNB55</field>
+ <field name="long_name">deafness, autosomal recessive 55</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q12-q13.2</field>
+ <field name="info">
+Deafness, autosomal recessive 55</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB59">
+ <field name="name">DFNB59</field>
+ <field name="long_name">deafness, autosomal recessive 59</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31.1-q31.3</field>
+ <field name="info">
+Deafness, autosomal recessive 59 [MIM:610220]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB5">
+ <field name="name">DFNB5</field>
+ <field name="long_name">deafness, autosomal recessive 5</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q12</field>
+ <field name="info">
+Deafness, autosomal recessive 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB62">
+ <field name="name">DFNB62</field>
+ <field name="long_name">deafness, autosomal recessive 62</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.2-p11.23</field>
+ <field name="info">
+Deafness, autosomal recessive 62</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB65">
+ <field name="name">DFNB65</field>
+ <field name="long_name">deafness, autosomal recessive 65</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.2-q13.3</field>
+ <field name="info">
+Deafness, autosomal recessive 65</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB66">
+ <field name="name">DFNB66</field>
+ <field name="long_name">deafness, autosomal recessive 66</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p22.3-p21.2</field>
+ <field name="info">
+Deafness, autosomal recessive 66</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNB72">
+ <field name="name">DFNB72</field>
+ <field name="long_name">deafness, autosomal recessive 72</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Deafness, autosomal recessive 72</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNM1">
+ <field name="name">DFNM1</field>
+ <field name="long_name">deafness (recessive, nonsyndromic) modifier 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q24</field>
+ <field name="info">
+Deafness, nonsyndromic, modifier 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DFNY1">
+ <field name="name">DFNY1</field>
+ <field name="long_name">deafness, Y-linked 1</field>
+ <field name="chromosome">Y</field>
+ <field name="location">Y</field>
+ <field name="info">
+Deafness, Y-linked 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DGAT1">
+ <field name="name">DGAT1</field>
+ <field name="long_name">diacylglycerol O-acyltransferase homolog 1 (mouse)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DGCR2">
+ <field name="name">DGCR2</field>
+ <field name="long_name">DiGeorge syndrome critical region gene 2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p14-p13</field>
+ <field name="info">
+DiGeorge syndrome/velocardiofacial syndrome complex-2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DGCR">
+ <field name="name">DGCR</field>
+ <field name="long_name">DiGeorge syndrome chromosome region</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+Conotruncal anomaly face syndrome [MIM:217095]
+DiGeorge syndrome [MIM:188400]
+Velocardiofacial syndrome [MIM:192430]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DGKD">
+ <field name="name">DGKD</field>
+ <field name="long_name">diacylglycerol kinase, delta 130kDa</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DGS2">
+ <field name="name">DGS2</field>
+ <field name="long_name">DiGeorge syndrome chromosome region-2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p14-p13</field>
+ <field name="info">
+DiGeorge syndrome/velocardiofacial syndrome complex-2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DGUOK">
+ <field name="name">DGUOK</field>
+ <field name="long_name">deoxyguanosine kinase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p13</field>
+ <field name="info">
+Mitochondrial DNA-depletion syndrome, hepatocerebral form [MIM:251880]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DHCR24">
+ <field name="name">DHCR24</field>
+ <field name="long_name">24-dehydrocholesterol reductase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p33-p31.1</field>
+ <field name="info">
+Desmosterolosis [MIM:602398]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DHCR7">
+ <field name="name">DHCR7</field>
+ <field name="long_name">7-dehydrocholesterol reductase</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q12-q13</field>
+ <field name="info">
+Smith-Lemli-Opitz syndrome [MIM:270400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DHFRP1">
+ <field name="name">DHFRP1</field>
+ <field name="long_name">dihydrofolate reductase pseudogene 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q11.2-q13.2</field>
+ <field name="info">
+Anemia, megaloblastic, due to DHFR deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DHFR">
+ <field name="name">DHFR</field>
+ <field name="long_name">dihydrofolate reductase</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q11.2-q13.2</field>
+ <field name="info">
+Anemia, megaloblastic, due to DHFR deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DHH">
+ <field name="name">DHH</field>
+ <field name="long_name">desert hedgehog homolog (Drosophila)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13.1</field>
+ <field name="info">
+Gonadal dysgenesis, 46XY, partial, with minifascicular neuropathy [MIM:607080]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DHOF">
+ <field name="name">DHOF</field>
+ <field name="long_name">dermal hypoplasia, focal</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23</field>
+ <field name="info">
+Focal dermal hypoplasia [MIM:305600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DHS">
+ <field name="name">DHS</field>
+ <field name="long_name">dehydrated hereditary stomatocytosis</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q23-q24</field>
+ <field name="info">
+Dehydrated hereditary stomatocytosis
+Pseudohyperkalemia, familial [MIM:177720]
+Dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema [MIM:603528]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DHX16">
+ <field name="name">DHX16</field>
+ <field name="long_name">DEAH (Asp-Glu-Ala-His) box polypeptide 16</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DHX36">
+ <field name="name">DHX36</field>
+ <field name="long_name">DEAH (Asp-Glu-Ala-His) box polypeptide 36</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q25.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DIAPH1">
+ <field name="name">DIAPH1</field>
+ <field name="long_name">diaphanous homolog 1 (Drosophila)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Deafness, autosomal dominant 1 [MIM:124900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DIAPH2">
+ <field name="name">DIAPH2</field>
+ <field name="long_name">diaphanous homolog 2 (Drosophila)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22</field>
+ <field name="info">
+Premature ovarian failure [MIM:300511]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DIH1">
+ <field name="name">DIH1</field>
+ <field name="long_name">diaphragmatic hernia 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26.1</field>
+ <field name="info">
+Hernia, congenital diaphragmatic 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DIH2">
+ <field name="name">DIH2</field>
+ <field name="long_name">Hernia, congenital diaphragmatic 2</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23.1</field>
+ <field name="info">
+Hernia, congenital diaphragmatic 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DIO1">
+ <field name="name">DIO1</field>
+ <field name="long_name">deiodinase, iodothyronine, type I</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p33-p32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DIO2">
+ <field name="name">DIO2</field>
+ <field name="long_name">deiodinase, iodothyronine, type II</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DIP2B">
+ <field name="name">DIP2B</field>
+ <field name="long_name">DIP2 disco-interacting protein 2 homolog B (Drosophila)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13.12</field>
+ <field name="info">
+Mental retardation, FRA12A type [MIM:136630]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DIRC2">
+ <field name="name">DIRC2</field>
+ <field name="long_name">disrupted in renal carcinoma 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21</field>
+ <field name="info">
+Renal cell carcinoma [MIM:144700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DISC1">
+ <field name="name">DISC1</field>
+ <field name="long_name">disrupted in schizophrenia 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42.1</field>
+ <field name="info">
+Schizophrenia, susceptibility to [MIM:604906]
+Schizoaffective disorder, susceptibility to [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DISC2">
+ <field name="name">DISC2</field>
+ <field name="long_name">disrupted in schizophrenia 2 (non-protein coding)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42.1</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DKBI">
+ <field name="name">DKBI</field>
+ <field name="long_name">Dyskeratosis, hereditary benign intraepithelial</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q35</field>
+ <field name="info">
+Dyskeratosis, hereditary benign intraepithelial</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DKC1">
+ <field name="name">DKC1</field>
+ <field name="long_name">dyskeratosis congenita 1, dyskerin</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Dyskeratosis congenita-1 [MIM:305000]
+Hoyeraal-Hreidarsson syndrome [MIM:300240]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DLAT">
+ <field name="name">DLAT</field>
+ <field name="long_name">dihydrolipoamide S-acetyltransferase</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.1</field>
+ <field name="info">
+Pyruvate dehydrogenase E2 deficiency [MIM:245348]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DLC1">
+ <field name="name">DLC1</field>
+ <field name="long_name">deleted in liver cancer 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p22-p21.3</field>
+ <field name="info">
+Colorectal cancer, somatic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DLD">
+ <field name="name">DLD</field>
+ <field name="long_name">dihydrolipoamide dehydrogenase</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31-q32</field>
+ <field name="info">
+Maple syrup urine disease, type III [MIM:248600]
+Leigh syndrome [MIM:256000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DLEC1">
+ <field name="name">DLEC1</field>
+ <field name="long_name">deleted in lung and esophageal cancer 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p22-p21.3</field>
+ <field name="info">
+Lung cancer [MIM:211980]
+Esophageal cancer [MIM:133239]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DLG3">
+ <field name="name">DLG3</field>
+ <field name="long_name">discs, large homolog 3 (Drosophila)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.1</field>
+ <field name="info">
+Mental retardation, X-linked-90</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DLG5">
+ <field name="name">DLG5</field>
+ <field name="long_name">discs, large homolog 5 (Drosophila)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23</field>
+ <field name="info">
+Crohn disease, susceptibility to [MIM:266600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DLL3">
+ <field name="name">DLL3</field>
+ <field name="long_name">delta-like 3 (Drosophila)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+Spondylocostal dysostosis, autosomal recessive, 1 [MIM:277300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DLX3">
+ <field name="name">DLX3</field>
+ <field name="long_name">distal-less homeobox 3</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.3-q22</field>
+ <field name="info">
+Trichodontoosseous syndrome [MIM:190320]
+Amelogenesis imperfecta, hypomaturation-hypoplastic type, with taurodontism [MIM:104510]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DMBT1">
+ <field name="name">DMBT1</field>
+ <field name="long_name">deleted in malignant brain tumors 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q25.3-q26.1</field>
+ <field name="info">
+Glioblastoma multiforme, somatic [MIM:137800]
+Medulloblastoma [MIM:155255]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DMC1">
+ <field name="name">DMC1</field>
+ <field name="long_name">DMC1 dosage suppressor of mck1 homolog, meiosis-specific homologous recombination (yeast)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DMD">
+ <field name="name">DMD</field>
+ <field name="long_name">dystrophin</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp21.2</field>
+ <field name="info">
+Duchenne muscular dystrophy [MIM:310200]
+Becker muscular dystrophy [MIM:300376]
+Cardiomyopathy, dilated, 3B [MIM:302045]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DMGDH">
+ <field name="name">DMGDH</field>
+ <field name="long_name">dimethylglycine dehydrogenase</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q12.2-q12.3</field>
+ <field name="info">
+Dimethylglycine dehydrogenase deficiency [MIM:605850]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DMP1">
+ <field name="name">DMP1</field>
+ <field name="long_name">dentin matrix acidic phosphoprotein 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21</field>
+ <field name="info">
+Hypophosphatemic rickets, AR [MIM:241520]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DMPK">
+ <field name="name">DMPK</field>
+ <field name="long_name">dystrophia myotonica-protein kinase</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2-q13.3</field>
+ <field name="info">
+Myotonic dystrophy [MIM:160900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DMRT1">
+ <field name="name">DMRT1</field>
+ <field name="long_name">doublesex and mab-3 related transcription factor 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p24.3</field>
+ <field name="info">
+XY sex reversal</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DNAH11">
+ <field name="name">DNAH11</field>
+ <field name="long_name">dynein, axonemal, heavy chain 11</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p21</field>
+ <field name="info">
+Ciliary dyskinesia, primary, 7, with out without situs inversus [MIM:611884]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DNAH5">
+ <field name="name">DNAH5</field>
+ <field name="long_name">dynein, axonemal, heavy chain 5</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15-p14</field>
+ <field name="info">
+Ciliary dyskinesia, primary, 3, with or without situs inversus [MIM:608644]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DNAH9">
+ <field name="name">DNAH9</field>
+ <field name="long_name">dynein, axonemal, heavy chain 9</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DNAI1">
+ <field name="name">DNAI1</field>
+ <field name="long_name">dynein, axonemal, intermediate chain 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21-p13</field>
+ <field name="info">
+Ciliary dyskinesia, primary, 1, with our without situs inversus [MIM:244400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DNAI2">
+ <field name="name">DNAI2</field>
+ <field name="long_name">dynein, axonemal, intermediate chain 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+Ciliary dyskinesia, primary, 9, with our without situs inversus [MIM:612444]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DNAJC19">
+ <field name="name">DNAJC19</field>
+ <field name="long_name">DnaJ (Hsp40) homolog, subfamily C, member 19</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.3</field>
+ <field name="info">
+3-methylglutaconic aciduria, type V [MIM:610198]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DNASE1">
+ <field name="name">DNASE1</field>
+ <field name="long_name">deoxyribonuclease I</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+Systemic lupus erythematosus, susceptibility to [MIM:152700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DNASE2">
+ <field name="name">DNASE2</field>
+ <field name="long_name">deoxyribonuclease II, lysosomal</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2-q13.4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DND1">
+ <field name="name">DND1</field>
+ <field name="long_name">dead end homolog 1 (zebrafish)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DNM1L">
+ <field name="name">DNM1L</field>
+ <field name="long_name">dynamin 1-like</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p11.21</field>
+ <field name="info">
+Encephalopahty, lethal, due to defective mitochondrial peroxisomal fission</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DNM2">
+ <field name="name">DNM2</field>
+ <field name="long_name">dynamin 2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, dominant intermediate B [MIM:606482]
+Myopathy, centronuclear [MIM:160150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DNMT3B">
+ <field name="name">DNMT3B</field>
+ <field name="long_name">DNA (cytosine-5-)-methyltransferase 3 beta</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11.2</field>
+ <field name="info">
+Immunodeficiency-centromeric instability-facial anomalies syndrome [MIM:242860]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DOCK3">
+ <field name="name">DOCK3</field>
+ <field name="long_name">dedicator of cytokinesis 3</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DOCK8">
+ <field name="name">DOCK8</field>
+ <field name="long_name">dedicator of cytokinesis 8</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p24</field>
+ <field name="info">
+Mental retardation, autosomal dominant 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DOK7">
+ <field name="name">DOK7</field>
+ <field name="long_name">docking protein 7</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.2</field>
+ <field name="info">
+Myasthenia, limb-girdle, familial [MIM:254300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DPM1">
+ <field name="name">DPM1</field>
+ <field name="long_name">dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunit</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.13</field>
+ <field name="info">
+Congenital disorder of glycosylation, type Ie [MIM:608799]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DPYD">
+ <field name="name">DPYD</field>
+ <field name="long_name">dihydropyrimidine dehydrogenase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p22</field>
+ <field name="info">
+Dihydropyrimidine dehydrogenase deficiency [MIM:274270]
+5-fluorouracil toxicity [MIM:274270]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DPYSL2">
+ <field name="name">DPYSL2</field>
+ <field name="long_name">dihydropyrimidinase-like 2</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DPYS">
+ <field name="name">DPYS</field>
+ <field name="long_name">dihydropyrimidinase</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q22</field>
+ <field name="info">
+Dihydropyrimidinuria</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DRD1">
+ <field name="name">DRD1</field>
+ <field name="long_name">dopamine receptor D1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q35.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DRD2">
+ <field name="name">DRD2</field>
+ <field name="long_name">dopamine receptor D2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.1</field>
+ <field name="info">
+Dystonia, myoclonic [MIM:159900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DRD3">
+ <field name="name">DRD3</field>
+ <field name="long_name">dopamine receptor D3</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q13.3</field>
+ <field name="info">
+Schizophrenia, susceptibility to [MIM:181500]
+Essential tremor, susceptibility to [MIM:190300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DRD4">
+ <field name="name">DRD4</field>
+ <field name="long_name">dopamine receptor D4</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Autonomic nervous system dysfunction
+Novelty seeking personality [MIM:601696]
+Attention deficit-hyperactivity disorder [MIM:143465]
+Parkinson disease, protection against [MIM:168600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DRD5">
+ <field name="name">DRD5</field>
+ <field name="long_name">dopamine receptor D5</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.1-p15.3</field>
+ <field name="info">
+Blepharospasm, primary benign [MIM:606798]
+Dystonia, primary cervical
+Attention deficit-hyperactivity disorder, susceptibility to [MIM:143465]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DSAP2">
+ <field name="name">DSAP2</field>
+ <field name="long_name">disseminated superficial actinic porokeratosis 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q25.1-q26.1</field>
+ <field name="info">
+Porokeratosis, disseminated superficial actinic, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DSAP3">
+ <field name="name">DSAP3</field>
+ <field name="long_name">Porokeratosis, disseminated superficial actinic, 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31.3-p31.1</field>
+ <field name="info">
+Porokeratosis, disseminated superficial actinic, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DSAP4">
+ <field name="name">DSAP4</field>
+ <field name="long_name">Porokeratosis, disseminated superficial actinic, 4</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.3</field>
+ <field name="info">
+Porokeratosis, disseminated superficial actinic, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DSC2">
+ <field name="name">DSC2</field>
+ <field name="long_name">desmocollin 2</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q12.1</field>
+ <field name="info">
+Arrhythmogenic right ventricular dysplasia, familial, 11 [MIM:610476]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DSCAM">
+ <field name="name">DSCAM</field>
+ <field name="long_name">Down syndrome cell adhesion molecule</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.2-q22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DSG1">
+ <field name="name">DSG1</field>
+ <field name="long_name">desmoglein 1</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q12.1-q12.2</field>
+ <field name="info">
+Keratosis palmoplantaris striata I [MIM:148700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DSG2">
+ <field name="name">DSG2</field>
+ <field name="long_name">desmoglein 2</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q12.1-q12.2</field>
+ <field name="info">
+Arrhythmogenic right ventricular dysplasia, familial, 10 [MIM:610193]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DSG4">
+ <field name="name">DSG4</field>
+ <field name="long_name">desmoglein 4</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q12</field>
+ <field name="info">
+Hypotrichosis, localized, autosomal recessive [MIM:607903]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DSPP">
+ <field name="name">DSPP</field>
+ <field name="long_name">dentin sialophosphoprotein</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21.3</field>
+ <field name="info">
+Dentinogenesis imperfecta, Shields type II [MIM:125490]
+Deafness, autosomal dominant 36, with dentinogenesis [MIM:605594]
+Dentinogenesis imperfecta, Shields type III [MIM:125500]
+Dentin dysplasia, type II [MIM:125420]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DSP">
+ <field name="name">DSP</field>
+ <field name="long_name">desmoplakin</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p24</field>
+ <field name="info">
+Keratosis palmoplantaris striata II
+Dilated cardiomyopathy with woolly hair and keratoderma [MIM:605676]
+Arrhythmogenic right ventricular dysplasia 8 [MIM:607450]
+Skin fragility-woolly hair syndrome [MIM:607655]
+Epidermolysis bullosa, lethal acantholytic [MIM:609638]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DST">
+ <field name="name">DST</field>
+ <field name="long_name">dystonin</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12-p11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DTNA">
+ <field name="name">DTNA</field>
+ <field name="long_name">dystrobrevin, alpha</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q12.1-q12.2</field>
+ <field name="info">
+Left ventricular noncompaction with congenital heart defects [MIM:606617]
+Left ventricular noncompaction, familial isolated, 1 [MIM:604169]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DTNBP1">
+ <field name="name">DTNBP1</field>
+ <field name="long_name">dystrobrevin binding protein 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p22.3</field>
+ <field name="info">
+Schizophrenia [MIM:181500]
+Hermansky-Pudlak syndrome 7 [MIM:203300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DUH2">
+ <field name="name">DUH2</field>
+ <field name="long_name">Dyschromatosis universalis hereditaria 2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q21-q23</field>
+ <field name="info">
+Dyschromatosis universalis hereditaria 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DUH">
+ <field name="name">DUH</field>
+ <field name="long_name">Dyschromatosis universalis hereditaria</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q24.2-q25.2</field>
+ <field name="info">
+Dyschromatosis universalis hereditaria 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DUOX2">
+ <field name="name">DUOX2</field>
+ <field name="long_name">dual oxidase 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15.3</field>
+ <field name="info">
+Hypothyroidism, congenital, due to DUOX2 deficiency [MIM:607200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DUOXA2">
+ <field name="name">DUOXA2</field>
+ <field name="long_name">dual oxidase maturation factor 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DUPC1">
+ <field name="name">DUPC1</field>
+ <field name="long_name">Dupuytren contracture 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q11.1-q22</field>
+ <field name="info">
+Dupuytren contracture 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DURS1">
+ <field name="name">DURS1</field>
+ <field name="long_name">Duane retraction syndrome 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q13</field>
+ <field name="info">
+Duane syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DUX4">
+ <field name="name">DUX4</field>
+ <field name="long_name">double homeobox, 4</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q35</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYM">
+ <field name="name">DYM</field>
+ <field name="long_name">dymeclin</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q12-q21.1</field>
+ <field name="info">
+Dyggve-Melchior-Clausen disease [MIM:223800]
+Smith-McCort dysplasia [MIM:607326]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYRK1A">
+ <field name="name">DYRK1A</field>
+ <field name="long_name">dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYSF">
+ <field name="name">DYSF</field>
+ <field name="long_name">dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p13.3-p13.1</field>
+ <field name="info">
+Muscular dystrophy, limb-girdle, type 2B [MIM:253601]
+Miyoshi myopathy [MIM:254130]
+Myopathy, distal, with anterior tibial onset [MIM:606768]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYT13">
+ <field name="name">DYT13</field>
+ <field name="long_name">dystonia 13, torsion</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.32-p36.13</field>
+ <field name="info">
+Dystonia 13, torsion</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYT15">
+ <field name="name">DYT15</field>
+ <field name="long_name">dystonia 15, myoclonic</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11</field>
+ <field name="info">
+Dystonia-15, myoclonic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYT17">
+ <field name="name">DYT17</field>
+ <field name="long_name">dystonia 17</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p11.2-q13.12</field>
+ <field name="info">
+Dystonia-17, primary torsion</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYT3">
+ <field name="name">DYT3</field>
+ <field name="long_name">dystonia 3 (with Parkinsonism)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13</field>
+ <field name="info">
+Dystonia-Parkinsonism, X-linked [MIM:314250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYT6">
+ <field name="name">DYT6</field>
+ <field name="long_name">dystonia 6, torsion (autosomal dominant)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p11.21</field>
+ <field name="info">
+Dystonia 6, torsion [MIM:602629]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYT7">
+ <field name="name">DYT7</field>
+ <field name="long_name">dystonia 7, torsion (autosomal dominant)</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p</field>
+ <field name="info">
+Dystonia-7, torsion</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYX1C1">
+ <field name="name">DYX1C1</field>
+ <field name="long_name">dyslexia susceptibility 1 candidate 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21</field>
+ <field name="info">
+Dyslexia, susceptibility to, 1 [MIM:127700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYX1">
+ <field name="name">DYX1</field>
+ <field name="long_name">dyslexia susceptibility 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21</field>
+ <field name="info">
+Dyslexia, susceptibility to, 1 [MIM:127700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYX2">
+ <field name="name">DYX2</field>
+ <field name="long_name">dyslexia susceptibility 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p22.2</field>
+ <field name="info">
+Dyslexia, susceptibility to, 2 [MIM:600202]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYX3">
+ <field name="name">DYX3</field>
+ <field name="long_name">dyslexia susceptibility 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p16-p15</field>
+ <field name="info">
+Dyslexia, susceptibility to, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYX5">
+ <field name="name">DYX5</field>
+ <field name="long_name">dyslexia susceptibility 5</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p12-q13</field>
+ <field name="info">
+Dyslexia, susceptibility to, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYX6">
+ <field name="name">DYX6</field>
+ <field name="long_name">dyslexia susceptibility 6</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.2</field>
+ <field name="info">
+Dyslexia, susceptibility to, 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYX8">
+ <field name="name">DYX8</field>
+ <field name="long_name">dyslexia susceptibility 8</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36-p34</field>
+ <field name="info">
+Dyslexia, susceptibility to, 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="DYX9">
+ <field name="name">DYX9</field>
+ <field name="long_name">dyslexia susceptibility 9</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq27.3</field>
+ <field name="info">
+Dyslexia, susceptibility to, 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EA3">
+ <field name="name">EA3</field>
+ <field name="long_name">Episodic ataxia, type 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42</field>
+ <field name="info">
+Episodic ataxia, type 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EA7">
+ <field name="name">EA7</field>
+ <field name="long_name">Episodic ataxia, type 7</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+Episodic ataxia, type 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EBP">
+ <field name="name">EBP</field>
+ <field name="long_name">emopamil binding protein (sterol isomerase)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23-p11.22</field>
+ <field name="info">
+Chondrodysplasia punctata, X-linked dominant [MIM:302960]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ECA1">
+ <field name="name">ECA1</field>
+ <field name="long_name">epilepsy, childhood absence 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24</field>
+ <field name="info">
+Epilepsy, childhood absence, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ECE1">
+ <field name="name">ECE1</field>
+ <field name="long_name">endothelin converting enzyme 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.1</field>
+ <field name="info">
+Hirschsprung disease, cardiac defects, and autonomic dysfunction
+Hypertension, essential, susceptibility to [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ECM1">
+ <field name="name">ECM1</field>
+ <field name="long_name">extracellular matrix protein 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Lipoid proteinosis [MIM:247100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EDARADD">
+ <field name="name">EDARADD</field>
+ <field name="long_name">EDAR-associated death domain</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42.2-q43</field>
+ <field name="info">
+Ectodermal dysplasia, anhidrotic, autosomal recessive [MIM:224900]
+Ectodermal dysplasia, anhidrotic, autosomal dominant [MIM:129490]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EDAR">
+ <field name="name">EDAR</field>
+ <field name="long_name">ectodysplasin A receptor</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q11-q13</field>
+ <field name="info">
+Ectodermal dysplasia, hypohidrotic, autosomal dominant [MIM:129490]
+Ectodermal dysplasia, hypohidrotic, autosomal recessive [MIM:224900]
+Hair morphology 1, hair thickness [MIM:612630]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EDA">
+ <field name="name">EDA</field>
+ <field name="long_name">ectodysplasin A</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq12-q13.1</field>
+ <field name="info">
+Ectodermal dysplasia, anhidrotic, X-linked [MIM:305100]
+Hypodontia, X-linked [MIM:300606]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EDN1">
+ <field name="name">EDN1</field>
+ <field name="long_name">endothelin 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p24-p23</field>
+ <field name="info">
+High density lipoprotein cholesterol level QTL 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EDN2">
+ <field name="name">EDN2</field>
+ <field name="long_name">endothelin 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="EDN3">
+ <field name="name">EDN3</field>
+ <field name="long_name">endothelin 3</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.2-q13.3</field>
+ <field name="info">
+Shah-Waardenburg syndrome [MIM:277580]
+Central hypoventilation syndrome, congenital [MIM:209880]
+Hirschsprung disease [MIM:142623]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EDNRA">
+ <field name="name">EDNRA</field>
+ <field name="long_name">endothelin receptor type A</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q31.2</field>
+ <field name="info">
+Migraine, resistance to [MIM:157300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EDNRB">
+ <field name="name">EDNRB</field>
+ <field name="long_name">endothelin receptor type B</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q22</field>
+ <field name="info">
+Hirschsprung disease-2 [MIM:600155]
+ABCD syndrome [MIM:600501]
+Waardenburg-Shah syndrome [MIM:277580]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EDS8">
+ <field name="name">EDS8</field>
+ <field name="long_name">Ehlers-Danlos syndrome, type VIII</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+Ehlers-Danlos syndrome, type VIII</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EEC1">
+ <field name="name">EEC1</field>
+ <field name="long_name">ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.2-q21.3</field>
+ <field name="info">
+EEC syndrome-1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EEF2K">
+ <field name="name">EEF2K</field>
+ <field name="long_name">eukaryotic elongation factor-2 kinase</field>
+ <field name="chromosome">16</field>
+ <field name="location">16</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="EFEMP1">
+ <field name="name">EFEMP1</field>
+ <field name="long_name">EGF-containing fibulin-like extracellular matrix protein 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p16</field>
+ <field name="info">
+Doyne honeycomb degeneration of retina [MIM:126600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EFEMP2">
+ <field name="name">EFEMP2</field>
+ <field name="long_name">EGF-containing fibulin-like extracellular matrix protein 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Cutis laxa, autosomal recessive, type I [MIM:219100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EFHC1">
+ <field name="name">EFHC1</field>
+ <field name="long_name">EF-hand domain (C-terminal) containing 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12-p11</field>
+ <field name="info">
+Myoclonic epilepsy, juvenile, 1 [MIM:254770]
+Epilepsy, juvenile absence [MIM:607631]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EFMR">
+ <field name="name">EFMR</field>
+ <field name="long_name">epilepsy, female restricted, with mental retardation (Juberg-Hellman syndrome)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.3</field>
+ <field name="info">
+Epilepsy, female-restricted, with mental retardation [MIM:300088]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EFNB1">
+ <field name="name">EFNB1</field>
+ <field name="long_name">ephrin-B1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq12</field>
+ <field name="info">
+Craniofrontonasal dysplasia [MIM:304110]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EGFR">
+ <field name="name">EGFR</field>
+ <field name="long_name">epidermal growth factor receptor (erythroblastic leukemia viral (v-erb-b) oncogene homolog, avian)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p12.3-p12.1</field>
+ <field name="info">
+Nonsmall cell lung cancer, response to tyrosine kinase inhibitor in [MIM:211980]
+Adenocarcinoma of lung, response to tyrosine kinase inhibitor in [MIM:211980]
+Nonsmall cell lung cancer, susceptibility to [MIM:211980]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EGF">
+ <field name="name">EGF</field>
+ <field name="long_name">epidermal growth factor (beta-urogastrone)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q25</field>
+ <field name="info">
+Hypomagnesemia 4, renal [MIM:611718]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EGLN1">
+ <field name="name">EGLN1</field>
+ <field name="long_name">egl nine homolog 1 (C. elegans)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42-q43</field>
+ <field name="info">
+Erythrocytosis, familial, 3 [MIM:609820]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EGR2">
+ <field name="name">EGR2</field>
+ <field name="long_name">early growth response 2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21.1-q22.1</field>
+ <field name="info">
+Neuropathy, congenital hypomyelinating, 1 [MIM:605253]
+Charcot-Marie-Tooth disease, type 1D [MIM:607678]
+Dejerine-Sottas neuropathy [MIM:145900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EGR3">
+ <field name="name">EGR3</field>
+ <field name="long_name">early growth response 3</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23-p21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="EHBP1">
+ <field name="name">EHBP1</field>
+ <field name="long_name">EH domain binding protein 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p15</field>
+ <field name="info">
+Prostate cancer, hereditary, 12 [MIM:611868]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EHMT1">
+ <field name="name">EHMT1</field>
+ <field name="long_name">euchromatic histone-lysine N-methyltransferase 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.3</field>
+ <field name="info">
+Chromosome 9q subtelomeric deletion syndrome [MIM:610253]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EIF2AK3">
+ <field name="name">EIF2AK3</field>
+ <field name="long_name">eukaryotic translation initiation factor 2-alpha kinase 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p12</field>
+ <field name="info">
+Wolcott-Rallison syndrome [MIM:226980]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EIF2B1">
+ <field name="name">EIF2B1</field>
+ <field name="long_name">eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa</field>
+ <field name="chromosome">12</field>
+ <field name="location">12</field>
+ <field name="info">
+Leukoencephalopathy with vanishing white matter [MIM:603896]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EIF2B2">
+ <field name="name">EIF2B2</field>
+ <field name="long_name">eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24</field>
+ <field name="info">
+Leukoencephalopathy with vanishing white matter [MIM:603896]
+Ovarioleukodystrophy [MIM:603896]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EIF2B3">
+ <field name="name">EIF2B3</field>
+ <field name="long_name">eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34.1</field>
+ <field name="info">
+Leukoencephalopathy with vanishing white matter [MIM:603896]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EIF2B4">
+ <field name="name">EIF2B4</field>
+ <field name="long_name">eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p23.3</field>
+ <field name="info">
+Leukoencephaly with vanishing white matter [MIM:603896]
+Ovarioleukodystrophy [MIM:603896]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EIF2B5">
+ <field name="name">EIF2B5</field>
+ <field name="long_name">eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27</field>
+ <field name="info">
+Leukoencephalopathy with vanishing white matter [MIM:603896]
+Ovarioleukodystrophy [MIM:603896]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EIG2">
+ <field name="name">EIG2</field>
+ <field name="long_name">Epilepsy, idiopathic generalized, susceptibility to 2</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q23</field>
+ <field name="info">
+Epilepsy, idiopathic generalized [MIM:600669]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EIG3">
+ <field name="name">EIG3</field>
+ <field name="long_name">Epilepsy, idiopathic generalized, susceptibility to 3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q32-q33</field>
+ <field name="info">
+Epilepsy, idiopathic generalized [MIM:600669]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EIG4">
+ <field name="name">EIG4</field>
+ <field name="long_name">Epilepsy, idiopathic generalized, susceptibility to 4</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q25-q26</field>
+ <field name="info">
+Epilepsy, idiopathic generalized, susceptibility to 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EIG5">
+ <field name="name">EIG5</field>
+ <field name="long_name">Epilepsy, idiopathic generalized, susceptibility to, 5</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p11.22</field>
+ <field name="info">
+Epilepsy, idiopathic generalized, susceptibility to, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EIM">
+ <field name="name">EIM</field>
+ <field name="long_name">Infantile myoclonic epilepsy</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13</field>
+ <field name="info">
+Epilepsy, myoclonic, infantile</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EJM1">
+ <field name="name">EJM1</field>
+ <field name="long_name">epilepsy, juvenile myoclonic 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12-p11</field>
+ <field name="info">
+Myoclonic epilepsy, juvenile, 1 [MIM:254770]
+Epilepsy, juvenile absence [MIM:607631]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EJM2">
+ <field name="name">EJM2</field>
+ <field name="long_name">epilepsy, juvenile myoclonic 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q14</field>
+ <field name="info">
+Epilepsy, juvenile myoclonic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EJM3">
+ <field name="name">EJM3</field>
+ <field name="long_name">Epilepsy, juvenile myoclonic 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21</field>
+ <field name="info">
+Epilepsy, juvenile myoclonic 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EJM4">
+ <field name="name">EJM4</field>
+ <field name="long_name">Myoclonic epilepsy, juvenile, 4</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q12-q14</field>
+ <field name="info">
+Myoclonic epilepsy, juvenile, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EKD2">
+ <field name="name">EKD2</field>
+ <field name="long_name">Episodic kinesigenic dyskinesia 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q13-q22.1</field>
+ <field name="info">
+Episodic kinesigenic dyskinesia 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EKV3">
+ <field name="name">EKV3</field>
+ <field name="long_name">erythrokeratodermia variabilis 3 (Kamouraska type)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22</field>
+ <field name="info">
+Erythrokeratodermia variabilis 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ELAC2">
+ <field name="name">ELAC2</field>
+ <field name="long_name">elaC homolog 2 (E. coli)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11</field>
+ <field name="info">
+Prostate cancer, susceptibility to [MIM:176807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ELAVL4">
+ <field name="name">ELAVL4</field>
+ <field name="long_name">ELAV (embryonic lethal, abnormal vision, Drosophila)-like 4 (Hu antigen D)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34</field>
+ <field name="info">
+Neuropathy, paraneoplastic sensory</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ELK1">
+ <field name="name">ELK1</field>
+ <field name="long_name">ELK1, member of ETS oncogene family</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ELL">
+ <field name="name">ELL</field>
+ <field name="long_name">elongation factor RNA polymerase II</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ELN">
+ <field name="name">ELN</field>
+ <field name="long_name">elastin</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.2</field>
+ <field name="info">
+Supravalvar aortic stenosis [MIM:185500]
+Cutis laxa, AD [MIM:123700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ELOVL4">
+ <field name="name">ELOVL4</field>
+ <field name="long_name">elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q14</field>
+ <field name="info">
+Stargardt disease 3 [MIM:600110]
+Macular dystrophy, autosomal dominant, chromosome 6-linked [MIM:600110]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ELP4">
+ <field name="name">ELP4</field>
+ <field name="long_name">elongation protein 4 homolog (S. cerevisiae)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="EMD">
+ <field name="name">EMD</field>
+ <field name="long_name">emerin</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Emery-Dreifuss muscular dystrophy [MIM:310300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EMWX">
+ <field name="name">EMWX</field>
+ <field name="long_name">episodic muscle weakness, X-linked</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3</field>
+ <field name="info">
+Episodic muscle weakness, X-linked</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EMX2">
+ <field name="name">EMX2</field>
+ <field name="long_name">empty spiracles homeobox 2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q26.1</field>
+ <field name="info">
+Schizencephaly [MIM:269160]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EN2">
+ <field name="name">EN2</field>
+ <field name="long_name">engrailed homeobox 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q36</field>
+ <field name="info">
+Autism, susceptibility to, 10 [MIM:611016]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ENAM">
+ <field name="name">ENAM</field>
+ <field name="long_name">enamelin</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21</field>
+ <field name="info">
+Amelogenesis imperfecta 2, hypoplastic local [MIM:104500]
+Amelogenesis imperfecta, type IC [MIM:204650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ENDO1">
+ <field name="name">ENDO1</field>
+ <field name="long_name">Endometriosis, susceptibility to, 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q26</field>
+ <field name="info">
+Endometriosis, susceptibility to, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ENFL2">
+ <field name="name">ENFL2</field>
+ <field name="long_name">Epilepsy, nocturnal frontal lobe, type 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q24</field>
+ <field name="info">
+Epilepsy, nocturnal frontal lobe, type 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ENG">
+ <field name="name">ENG</field>
+ <field name="long_name">endoglin</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.1</field>
+ <field name="info">
+Hereditary hemorrhagic telangiectasia-1 [MIM:187300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ENO1">
+ <field name="name">ENO1</field>
+ <field name="long_name">enolase 1, (alpha)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1pter-p36.13</field>
+ <field name="info">
+Enolase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ENO3">
+ <field name="name">ENO3</field>
+ <field name="long_name">enolase 3 (beta, muscle)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17pter-p12</field>
+ <field name="info">
+Enolase-beta deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ENPP1">
+ <field name="name">ENPP1</field>
+ <field name="long_name">ectonucleotide pyrophosphatase/phosphodiesterase 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q22-q23</field>
+ <field name="info">
+Ossification of posterior longitudinal ligament of spine [MIM:602475]
+Diabetes mellitus, non-insulin-dependent, susceptibility to [MIM:125853]
+Obesity, susceptibility to [MIM:601665]
+Arterial calcification, generalized, of infancy [MIM:208000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ENSA">
+ <field name="name">ENSA</field>
+ <field name="long_name">endosulfine alpha</field>
+ <field name="chromosome">1</field>
+ <field name="location">1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ENUR1">
+ <field name="name">ENUR1</field>
+ <field name="long_name">enuresis, nocturnal 1</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q13-q14.3</field>
+ <field name="info">
+Enuresis, nocturnal, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ENUR2">
+ <field name="name">ENUR2</field>
+ <field name="long_name">enuresis, nocturnal 2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13-q21</field>
+ <field name="info">
+Enuresis, nocturnal, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EOMES">
+ <field name="name">EOMES</field>
+ <field name="long_name">eomesodermin homolog (Xenopus laevis)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.3-p21.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="EOS">
+ <field name="name">EOS</field>
+ <field name="long_name">eosinophilia, familial</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31-q33</field>
+ <field name="info">
+Eosinophilia, familial</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EP300">
+ <field name="name">EP300</field>
+ <field name="long_name">E1A binding protein p300</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13</field>
+ <field name="info">
+Colorectal cancer [MIM:114500]
+Rubinstein-Taybi syndrome [MIM:180849]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPAS1">
+ <field name="name">EPAS1</field>
+ <field name="long_name">endothelial PAS domain protein 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p21-p16</field>
+ <field name="info">
+Erythrocytosis, familial, 4 [MIM:611783]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPB41">
+ <field name="name">EPB41</field>
+ <field name="long_name">erythrocyte membrane protein band 4.1 (elliptocytosis 1, RH-linked)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2-p34</field>
+ <field name="info">
+Elliptocytosis-1 [MIM:611804]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPB42">
+ <field name="name">EPB42</field>
+ <field name="long_name">erythrocyte membrane protein band 4.2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15</field>
+ <field name="info">
+Spherocytosis, hereditary, type 5 [MIM:612690]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPHA2">
+ <field name="name">EPHA2</field>
+ <field name="long_name">EPH receptor A2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPHA5">
+ <field name="name">EPHA5</field>
+ <field name="long_name">EPH receptor A5</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPHB2">
+ <field name="name">EPHB2</field>
+ <field name="long_name">EPH receptor B2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.1-p35</field>
+ <field name="info">
+Prostate cancer, progression and metastasis of [MIM:603688]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPHX1">
+ <field name="name">EPHX1</field>
+ <field name="long_name">epoxide hydrolase 1, microsomal (xenobiotic)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42.1</field>
+ <field name="info">
+Fetal hydantoin syndrome
+Diphenylhydantoin toxicity
+Hypercholanemia, familial [MIM:607748]
+Preeclampsia, susceptibility to [MIM:189800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPHX2">
+ <field name="name">EPHX2</field>
+ <field name="long_name">epoxide hydrolase 2, cytoplasmic</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21-p12</field>
+ <field name="info">
+Hypercholesterolemia, familial, due to LDLR defect, modifier of [MIM:143890]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPM2A">
+ <field name="name">EPM2A</field>
+ <field name="long_name">epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q24</field>
+ <field name="info">
+Epilepsy, myoclonic, Lafora type [MIM:254780]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPOLM">
+ <field name="name">EPOLM</field>
+ <field name="long_name">epilepsy, occipitotemporal lobe, and migraine with aura</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q21-q22</field>
+ <field name="info">
+Epilepsy, occipitotemporal lobe, and migraine with aura</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPOR">
+ <field name="name">EPOR</field>
+ <field name="long_name">erythropoietin receptor</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3-p13.2</field>
+ <field name="info">
+Erythrocytosis, familial [MIM:133100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPO">
+ <field name="name">EPO</field>
+ <field name="long_name">erythropoietin</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21</field>
+ <field name="info">
+Microvascular complications of diabetes 2 [MIM:612623]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPPS">
+ <field name="name">EPPS</field>
+ <field name="long_name">Epilepsy, partial, with pericentral spikes</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15</field>
+ <field name="info">
+Epilepsy, partial, with pericentral spikes</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPRPDC">
+ <field name="name">EPRPDC</field>
+ <field name="long_name">Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12-p11.2</field>
+ <field name="info">
+Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EPX">
+ <field name="name">EPX</field>
+ <field name="long_name">eosinophil peroxidase</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23.1</field>
+ <field name="info">
+Eosinophil peroxidase deficiency [MIM:261500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ERBB2">
+ <field name="name">ERBB2</field>
+ <field name="long_name">v-erb-b2 erythroblastic leukemia viral oncogene homolog 2, neuro/glioblastoma derived oncogene homolog (avian)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.1</field>
+ <field name="info">
+Adenocarcinoma of lung, somatic [MIM:211980]
+Glioblastoma, somatic [MIM:137800]
+Gastric cancer, somatic [MIM:137215]
+Ovarian cancer, somatic </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ERBB3">
+ <field name="name">ERBB3</field>
+ <field name="long_name">v-erb-b2 erythroblastic leukemia viral oncogene homolog 3 (avian)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Lethal congenital contractural syndrome 2 [MIM:607598]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ERBB4">
+ <field name="name">ERBB4</field>
+ <field name="long_name">v-erb-a erythroblastic leukemia viral oncogene homolog 4 (avian)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33.3-q34</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ERCC1">
+ <field name="name">ERCC1</field>
+ <field name="long_name">excision repair cross-complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2-q13.3</field>
+ <field name="info">
+Cerebrooculofacioskeletal syndrome 4 [MIM:610758]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ERCC2">
+ <field name="name">ERCC2</field>
+ <field name="long_name">excision repair cross-complementing rodent repair deficiency, complementation group 2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2-q13.3</field>
+ <field name="info">
+Xeroderma pigmentosum, group D [MIM:278730]
+Trichothiodystrophy [MIM:601675]
+Cerebrooculofacioskeletal syndrome 2 [MIM:610756]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ERCC3">
+ <field name="name">ERCC3</field>
+ <field name="long_name">excision repair cross-complementing rodent repair deficiency, complementation group 3 (xeroderma pigmentosum group B complementing)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q21</field>
+ <field name="info">
+Xeroderma pigmentosum, group B [MIM:610651]
+Trichothiodystrophy [MIM:601675]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ERCC4">
+ <field name="name">ERCC4</field>
+ <field name="long_name">excision repair cross-complementing rodent repair deficiency, complementation group 4</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3-p13.13</field>
+ <field name="info">
+Xeroderma pigmentosum, group F [MIM:278760]
+XFE progeroid syndrome [MIM:610965]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ERCC5">
+ <field name="name">ERCC5</field>
+ <field name="long_name">excision repair cross-complementing rodent repair deficiency, complementation group 5</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q33</field>
+ <field name="info">
+Xeroderma pigmentosum, group G [MIM:278780]
+Cerebrooculofacioskeletal syndrome 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ERCC6">
+ <field name="name">ERCC6</field>
+ <field name="long_name">excision repair cross-complementing rodent repair deficiency, complementation group 6</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q11</field>
+ <field name="info">
+Cockayne syndrome, type B [MIM:133540]
+Cerebrooculofacioskeletal syndrome 1 [MIM:214150]
+De Sanctis-Cacchione syndrome [MIM:278800]
+Macular degeneration, age-related, susceptibility to 5
+Lung cancer [MIM:211980]
+UV-sensitive syndrome [MIM:600630]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ERCC8">
+ <field name="name">ERCC8</field>
+ <field name="long_name">excision repair cross-complementing rodent repair deficiency, complementation group 8</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q12</field>
+ <field name="info">
+Cockayne syndrome, type A [MIM:216400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ERF">
+ <field name="name">ERF</field>
+ <field name="long_name">Ets2 repressor factor</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ERMAP">
+ <field name="name">ERMAP</field>
+ <field name="long_name">erythroblast membrane-associated protein (Scianna blood group)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34</field>
+ <field name="info">
+Blood group, Scianna system [MIM:111750]
+Blood group, Radin [MIM:111620]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ESCO2">
+ <field name="name">ESCO2</field>
+ <field name="long_name">establishment of cohesion 1 homolog 2 (S. cerevisiae)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21.1</field>
+ <field name="info">
+Roberts syndrome [MIM:268300]
+SC phocomelia syndrome [MIM:269000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ESPN">
+ <field name="name">ESPN</field>
+ <field name="long_name">espin</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3-p36.1</field>
+ <field name="info">
+Deafness, autosomal recessive 36 [MIM:609006]
+Deafness, neurosensory, without vestibular involvement, autosomal dominant</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ESR1">
+ <field name="name">ESR1</field>
+ <field name="long_name">estrogen receptor 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25.1</field>
+ <field name="info">
+Breast cancer
+Estrogen resistance
+HDL response to hormone replacement, augmented
+Migraine, susceptibility to [MIM:157300]
+Atherosclerosis, susceptibility to
+Myocardial infarction, susceptibility to [MIM:608446]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ESR2">
+ <field name="name">ESR2</field>
+ <field name="long_name">estrogen receptor 2 (ER beta)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ESRRB">
+ <field name="name">ESRRB</field>
+ <field name="long_name">estrogen-related receptor beta</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3</field>
+ <field name="info">
+Deafness, autosomal recessive 35 [MIM:608565]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ETFA">
+ <field name="name">ETFA</field>
+ <field name="long_name">electron-transfer-flavoprotein, alpha polypeptide</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q23-q25</field>
+ <field name="info">
+Glutaricaciduria, type IIA [MIM:231680]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ETFB">
+ <field name="name">ETFB</field>
+ <field name="long_name">electron-transfer-flavoprotein, beta polypeptide</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+Glutaricaciduria, type IIB [MIM:231680]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ETFDH">
+ <field name="name">ETFDH</field>
+ <field name="long_name">electron-transferring-flavoprotein dehydrogenase</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q32-qter</field>
+ <field name="info">
+Glutaricaciduria, type IIC [MIM:231680]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ETHE1">
+ <field name="name">ETHE1</field>
+ <field name="long_name">ethylmalonic encephalopathy 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.32</field>
+ <field name="info">
+Ethylmalonic encephalopathy [MIM:602473]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ETL2">
+ <field name="name">ETL2</field>
+ <field name="long_name">epilepsy, familial temporal lobe</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q22-q23.3</field>
+ <field name="info">
+Epilepsy, familial temporal lobe</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ETM1">
+ <field name="name">ETM1</field>
+ <field name="long_name">essential tremor 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q13.3</field>
+ <field name="info">
+Schizophrenia, susceptibility to [MIM:181500]
+Essential tremor, susceptibility to [MIM:190300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ETM2">
+ <field name="name">ETM2</field>
+ <field name="long_name">essential tremor 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p25-p22</field>
+ <field name="info">
+Tremor, hereditary essential, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ETV6">
+ <field name="name">ETV6</field>
+ <field name="long_name">ets variant 6</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+Leukemia, acute myeloid, somatic [MIM:601626]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EVC2">
+ <field name="name">EVC2</field>
+ <field name="long_name">Ellis van Creveld syndrome 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16</field>
+ <field name="info">
+Ellis-van Creveld syndrome [MIM:225500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EVC">
+ <field name="name">EVC</field>
+ <field name="long_name">Ellis van Creveld syndrome</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16</field>
+ <field name="info">
+Ellis-van Creveld syndrome [MIM:225500]
+Weyers acrodental dysostosis [MIM:193530]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EVI1">
+ <field name="name">EVI1</field>
+ <field name="long_name">ecotropic viral integration site 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26</field>
+ <field name="info">
+3q21q26 syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EVR3">
+ <field name="name">EVR3</field>
+ <field name="long_name">exudative vitreoretinopathy 3</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13-p12</field>
+ <field name="info">
+Exudative vitreoretinopathy-3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EWSR1">
+ <field name="name">EWSR1</field>
+ <field name="long_name">Ewing sarcoma breakpoint region 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12</field>
+ <field name="info">
+Ewing sarcoma [MIM:612219]
+Neuroepithelioma [MIM:612219]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EXO1">
+ <field name="name">EXO1</field>
+ <field name="long_name">exonuclease 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42-q43</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="EXT1">
+ <field name="name">EXT1</field>
+ <field name="long_name">exostoses (multiple) 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.11-q24.13</field>
+ <field name="info">
+Exostoses, multiple, type 1 [MIM:133700]
+Chondrosarcoma [MIM:215300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EXT2">
+ <field name="name">EXT2</field>
+ <field name="long_name">exostoses (multiple) 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p12-p11</field>
+ <field name="info">
+Exostoses, multiple, type 2 [MIM:133701]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EXT3">
+ <field name="name">EXT3</field>
+ <field name="long_name">exostoses (multiple) 3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p</field>
+ <field name="info">
+Exostoses, multiple, type 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EYA1">
+ <field name="name">EYA1</field>
+ <field name="long_name">eyes absent homolog 1 (Drosophila)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q13.3</field>
+ <field name="info">
+Branchiootorenal syndrome [MIM:113650]
+Branchiootic syndrome
+Anterior segment anomalies and cataract
+Branchiootorenal syndrome with cataract [MIM:113650]
+Otofaciocervical syndrome [MIM:166780]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EYA4">
+ <field name="name">EYA4</field>
+ <field name="long_name">eyes absent homolog 4 (Drosophila)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23</field>
+ <field name="info">
+Deafness, autosomal dominant 10 [MIM:601316]
+Cardiomyopathy, dilated, 1J [MIM:605362]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="EYS">
+ <field name="name">EYS</field>
+ <field name="long_name">eyes shut homolog (Drosophila)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q12</field>
+ <field name="info">
+Retinitis pigmentosa-25 [MIM:602772]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="F10">
+ <field name="name">F10</field>
+ <field name="long_name">coagulation factor X</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q34</field>
+ <field name="info">
+Factor X deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="F11">
+ <field name="name">F11</field>
+ <field name="long_name">coagulation factor XI</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q35</field>
+ <field name="info">
+Factor XI deficiency, autosomal recessive [MIM:612416]
+Factor XI deficiency, autosomal dominant [MIM:612416]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="F12">
+ <field name="name">F12</field>
+ <field name="long_name">coagulation factor XII (Hageman factor)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q33-qter</field>
+ <field name="info">
+Factor XII deficiency [MIM:234000]
+Angioedema, hereditary, type III [MIM:610618]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="F13A1">
+ <field name="name">F13A1</field>
+ <field name="long_name">coagulation factor XIII, A1 polypeptide</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p25-p24</field>
+ <field name="info">
+Factor XIIIA deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="F13B">
+ <field name="name">F13B</field>
+ <field name="long_name">coagulation factor XIII, B polypeptide</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31-q32.1</field>
+ <field name="info">
+Factor XIIIB deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="F2R">
+ <field name="name">F2R</field>
+ <field name="long_name">coagulation factor II (thrombin) receptor</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="F2">
+ <field name="name">F2</field>
+ <field name="long_name">coagulation factor II (thrombin)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p11-q12</field>
+ <field name="info">
+Hypoprothrombinemia
+Dysprothrombinemia
+Hyperprothrombinemia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="F3">
+ <field name="name">F3</field>
+ <field name="long_name">coagulation factor III (thromboplastin, tissue factor)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p22-p21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="F5">
+ <field name="name">F5</field>
+ <field name="long_name">coagulation factor V (proaccelerin, labile factor)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23</field>
+ <field name="info">
+Factor V deficiency [MIM:227400]
+Thrombophilia, susceptibility to, due to factor V Leiden [MIM:188055]
+Stroke, ischemic, susceptiblity to [MIM:601367]
+Budd-Chiari syndrome [MIM:600880]
+Thrombophilia, susceptiblity to, due to activated protein C resistance [MIM:188055]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="F7">
+ <field name="name">F7</field>
+ <field name="long_name">coagulation factor VII (serum prothrombin conversion accelerator)</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q34</field>
+ <field name="info">
+Factor VII deficiency
+Myocardial infarction, decreased susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="F8">
+ <field name="name">F8</field>
+ <field name="long_name">coagulation factor VIII, procoagulant component</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Hemophilia A</field>
+</record>
+<record model="gnuhealth.disease.gene" id="F9">
+ <field name="name">F9</field>
+ <field name="long_name">coagulation factor IX</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq27.1-q27.2</field>
+ <field name="info">
+Hemophilia B [MIM:306900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FA2H">
+ <field name="name">FA2H</field>
+ <field name="long_name">fatty acid 2-hydroxylase</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q23</field>
+ <field name="info">
+Leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia [MIM:612443]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FAAH">
+ <field name="name">FAAH</field>
+ <field name="long_name">fatty acid amide hydrolase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p35-p34</field>
+ <field name="info">
+Drug addiction, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FABP1">
+ <field name="name">FABP1</field>
+ <field name="long_name">fatty acid binding protein 1, liver</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FABP2">
+ <field name="name">FABP2</field>
+ <field name="long_name">fatty acid binding protein 2, intestinal</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q28-q31</field>
+ <field name="info">
+insulin resistance,increased fatty oxidation in Pima Indian population (FABP2 polymorphism,A94T)</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FABP3">
+ <field name="name">FABP3</field>
+ <field name="long_name">fatty acid binding protein 3, muscle and heart (mammary-derived growth inhibitor)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p33-p31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FABP4">
+ <field name="name">FABP4</field>
+ <field name="long_name">fatty acid binding protein 4, adipocyte</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FAH">
+ <field name="name">FAH</field>
+ <field name="long_name">fumarylacetoacetate hydrolase (fumarylacetoacetase)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q23-q25</field>
+ <field name="info">
+Tyrosinemia, type I</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FAM123B">
+ <field name="name">FAM123B</field>
+ <field name="long_name">family with sequence similarity 123B</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq11.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FAM126A">
+ <field name="name">FAM126A</field>
+ <field name="long_name">family with sequence similarity 126, member A</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15.3</field>
+ <field name="info">
+Leukodystrophy, hypolyelinating, 5 [MIM:610532]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FAM20C">
+ <field name="name">FAM20C</field>
+ <field name="long_name">family with sequence similarity 20, member C</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p22</field>
+ <field name="info">
+Raine syndrome [MIM:259775]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FAM58A">
+ <field name="name">FAM58A</field>
+ <field name="long_name">family with sequence similarity 58, member A</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+STAR syndrome [MIM:300707]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FAM83H">
+ <field name="name">FAM83H</field>
+ <field name="long_name">family with sequence similarity 83, member H</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.3</field>
+ <field name="info">
+Amelogenesis imperfecta, type 3 [MIM:130900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FANCA">
+ <field name="name">FANCA</field>
+ <field name="long_name">Fanconi anemia, complementation group A</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.3</field>
+ <field name="info">
+Fanconi anemia, complementation group A [MIM:227650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FANCB">
+ <field name="name">FANCB</field>
+ <field name="long_name">Fanconi anemia, complementation group B</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.31</field>
+ <field name="info">
+Fanconi anemia, complementation group B [MIM:300514]
+VACTERL association with hydrocephalus, X-linked [MIM:314390]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FANCC">
+ <field name="name">FANCC</field>
+ <field name="long_name">Fanconi anemia, complementation group C</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22.3</field>
+ <field name="info">
+Fanconi anemia, complementation group C</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FANCD2">
+ <field name="name">FANCD2</field>
+ <field name="long_name">Fanconi anemia, complementation group D2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25.3</field>
+ <field name="info">
+Fanconi anemia, complementation group D2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FANCE">
+ <field name="name">FANCE</field>
+ <field name="long_name">Fanconi anemia, complementation group E</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p22-p21</field>
+ <field name="info">
+Fanconi anemia, complementation group E</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FANCF">
+ <field name="name">FANCF</field>
+ <field name="long_name">Fanconi anemia, complementation group F</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15</field>
+ <field name="info">
+Fanconi anemia, complementation group F</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FANCG">
+ <field name="name">FANCG</field>
+ <field name="long_name">Fanconi anemia, complementation group G</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p13</field>
+ <field name="info">
+Fanconi anemia, complementation group G</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FANCI">
+ <field name="name">FANCI</field>
+ <field name="long_name">Fanconi anemia, complementation group I</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q25-q26</field>
+ <field name="info">
+Fanconi anemia, complementation group I [MIM:608053]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FANCL">
+ <field name="name">FANCL</field>
+ <field name="long_name">Fanconi anemia, complementation group L</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p16.1</field>
+ <field name="info">
+Fanconi anemia, complementation group L</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FANCM">
+ <field name="name">FANCM</field>
+ <field name="long_name">Fanconi anemia, complementation group M</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q21.3</field>
+ <field name="info">
+Fanconi anemia, complementation group M</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FASN">
+ <field name="name">FASN</field>
+ <field name="long_name">fatty acid synthase</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FASTKD2">
+ <field name="name">FASTKD2</field>
+ <field name="long_name">FAST kinase domains 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33.3</field>
+ <field name="info">
+Mitochondrial complex IV deficiency [MIM:220110]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FAS">
+ <field name="name">FAS</field>
+ <field name="long_name">Fas (TNF receptor superfamily, member 6)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Autoimmune Lymphoproliferative Syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FBLN1">
+ <field name="name">FBLN1</field>
+ <field name="long_name">fibulin 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.3</field>
+ <field name="info">
+Synpolydactyly, 3/3'4, associated with metacarpal and metatarsal synostoses [MIM:608180]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FBLN5">
+ <field name="name">FBLN5</field>
+ <field name="long_name">fibulin 5</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.1</field>
+ <field name="info">
+Cutis laxa, autosomal recessive [MIM:219100]
+Cutis laxa, autosomal dominant [MIM:123700]
+Macular degeneration, age-related, 3 [MIM:608895]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FBN1">
+ <field name="name">FBN1</field>
+ <field name="long_name">fibrillin 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21.1</field>
+ <field name="info">
+Marfan syndrome [MIM:154700]
+Shprintzen-Goldberg syndrome [MIM:182212]
+Ectopia lentis, familial [MIM:129600]
+MASS syndrome [MIM:604308]
+Weill-Marchesani syndrome, dominant [MIM:608328]
+Aortic aneurysm, ascending, and dissection</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FBN2">
+ <field name="name">FBN2</field>
+ <field name="long_name">fibrillin 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q23-q31</field>
+ <field name="info">
+Contractural arachnodactyly, congenital [MIM:121050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FBP1">
+ <field name="name">FBP1</field>
+ <field name="long_name">fructose-1,6-bisphosphatase 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22.2-q22.3</field>
+ <field name="info">
+Fructose-1,6-bidphosphatase deficiency [MIM:229700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FBXO33">
+ <field name="name">FBXO33</field>
+ <field name="long_name">F-box protein 33</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q13.3</field>
+ <field name="info">
+Bone mineral density QTL 12 [MIM:612560]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FBXO7">
+ <field name="name">FBXO7</field>
+ <field name="long_name">F-box protein 7</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12-q13</field>
+ <field name="info">
+Parkinson disease 15, autosomal recessive [MIM:260300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FBXW11">
+ <field name="name">FBXW11</field>
+ <field name="long_name">F-box and WD repeat domain containing 11</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q35.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FBXW4">
+ <field name="name">FBXW4</field>
+ <field name="long_name">F-box and WD repeat domain containing 4</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FCAR">
+ <field name="name">FCAR</field>
+ <field name="long_name">Fc fragment of IgA, receptor for</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FCER1A">
+ <field name="name">FCER1A</field>
+ <field name="long_name">Fc fragment of IgE, high affinity I, receptor for; alpha polypeptide</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FCGR1A">
+ <field name="name">FCGR1A</field>
+ <field name="long_name">Fc fragment of IgG, high affinity Ia, receptor (CD64)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21.2-q21.3</field>
+ <field name="info">
+IgG receptor I, phagocytic, familial deficiency of</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FCGR2A">
+ <field name="name">FCGR2A</field>
+ <field name="long_name">Fc fragment of IgG, low affinity IIa, receptor (CD32)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21-q23</field>
+ <field name="info">
+Lupus nephritis, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FCGR2B">
+ <field name="name">FCGR2B</field>
+ <field name="long_name">Fc fragment of IgG, low affinity IIb, receptor (CD32)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q22</field>
+ <field name="info">
+Systemic lupus erythematosus, susceptibility to [MIM:152700]
+Malaria, resistance to [MIM:611162]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FCGR2C">
+ <field name="name">FCGR2C</field>
+ <field name="long_name">Fc fragment of IgG, low affinity IIc, receptor for (CD32)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23</field>
+ <field name="info">
+Thrombocytopenic purpura, autoimmune [MIM:188030]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FCGR3A">
+ <field name="name">FCGR3A</field>
+ <field name="long_name">Fc fragment of IgG, low affinity IIIa, receptor (CD16a)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23</field>
+ <field name="info">
+Lupus erythematosus, systemic, susceptibility [MIM:152700]
+Neutropenia, alloimmune neonatal
+Viral infections, recurrent</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FCGR3B">
+ <field name="name">FCGR3B</field>
+ <field name="long_name">Fc fragment of IgG, low affinity IIIb, receptor (CD16b)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23</field>
+ <field name="info">
+autoimmune thyroiditis,recurrent bacterial infections in some FCGR3B deficient people</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FCGRT">
+ <field name="name">FCGRT</field>
+ <field name="long_name">Fc fragment of IgG, receptor, transporter, alpha</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FCN2">
+ <field name="name">FCN2</field>
+ <field name="long_name">ficolin (collagen/fibrinogen domain containing lectin) 2 (hucolin)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FCN3">
+ <field name="name">FCN3</field>
+ <field name="long_name">ficolin (collagen/fibrinogen domain containing) 3 (Hakata antigen)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FCP1">
+ <field name="name">FCP1</field>
+ <field name="long_name">F-cell production 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.2</field>
+ <field name="info">
+Fetal hemoglobin quantitative trait locus 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FDFT1">
+ <field name="name">FDFT1</field>
+ <field name="long_name">farnesyl-diphosphate farnesyltransferase 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23.1-p22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="01/02/10">
+ <field name="name">01/02/10</field>
+ <field name="long_name">Febrile convulsions, familial, 10</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.2-q26.33</field>
+ <field name="info">
+Febrile convulsions, familial, 10</field>
+</record>
+<record model="gnuhealth.disease.gene" id="01/02/01">
+ <field name="name">01/02/01</field>
+ <field name="long_name">febrile convulsions 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q13-q21</field>
+ <field name="info">
+Convulsions, familial febrile, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="01/02/02">
+ <field name="name">01/02/02</field>
+ <field name="long_name">febrile convulsions 2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Convulsions, familial febrile, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="01/02/04">
+ <field name="name">01/02/04</field>
+ <field name="long_name">febrile convulsions 4</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q14</field>
+ <field name="info">
+Convulsions, familial febrile, 4 [MIM:604352]
+Usher syndrome, type IIC [MIM:605472]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="01/02/05">
+ <field name="name">01/02/05</field>
+ <field name="long_name">febrile convulsions 5</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q22-q24</field>
+ <field name="info">
+Febrile convulsions, familial, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="01/02/06">
+ <field name="name">01/02/06</field>
+ <field name="long_name">febrile convulsions 6</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.2</field>
+ <field name="info">
+Febrile convulsions, familial, 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="01/02/07">
+ <field name="name">01/02/07</field>
+ <field name="long_name">febrile convulsions 7</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22</field>
+ <field name="info">
+Febrile convulsions, familial, 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="01/02/09">
+ <field name="name">01/02/09</field>
+ <field name="long_name">Febrile convulsions, familial, 9</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p24.2-p23</field>
+ <field name="info">
+Febrile convulsions, familial, 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FECH">
+ <field name="name">FECH</field>
+ <field name="long_name">ferrochelatase (protoporphyria)</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.3</field>
+ <field name="info">
+Protoporphyria, erythropoietic, autosomal dominant [MIM:177000]
+Protoporphyria, erythropoietic, autosomal recessive [MIM:177000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FEOM3A">
+ <field name="name">FEOM3A</field>
+ <field name="long_name">Fibrosis of extraocular muscles, congenital, 3A</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p11.2-q12</field>
+ <field name="info">
+Fibrosis of extraocular muscles, congenital, 3A</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FEOM3">
+ <field name="name">FEOM3</field>
+ <field name="long_name">fibrosis of extraocular muscles, congenital, 3</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.2-q24.3</field>
+ <field name="info">
+Fibrosis of extraocular muscles, congenital, 3
+Fibrosis, congenital, of vertically acting extraocular muscles</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FER">
+ <field name="name">FER</field>
+ <field name="long_name">fer (fps/fes related) tyrosine kinase</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q21-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FES">
+ <field name="name">FES</field>
+ <field name="long_name">feline sarcoma oncogene</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FEV">
+ <field name="name">FEV</field>
+ <field name="long_name">FEV (ETS oncogene family)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGA">
+ <field name="name">FGA</field>
+ <field name="long_name">fibrinogen alpha chain</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q28</field>
+ <field name="info">
+Dysfibrinogenemia, alpha type, causing bleeding diathesis
+Dysfibrinogenemia, alpha type, causing recurrent thrombosis
+Amyloidosis, hereditary renal [MIM:105200]
+Afibrinogenemia, congenital [MIM:202400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGB">
+ <field name="name">FGB</field>
+ <field name="long_name">fibrinogen beta chain</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q28</field>
+ <field name="info">
+Dysfibrinogenemia, beta type
+Afibrinogenemia, congenital [MIM:202400]
+Thrombophilia, dysfibrinogenemic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGD1">
+ <field name="name">FGD1</field>
+ <field name="long_name">FYVE, RhoGEF and PH domain containing 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.21</field>
+ <field name="info">
+Aarskog-Scott syndrome [MIM:305400]
+Mental retardation, X-linked nonsyndromic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGD2">
+ <field name="name">FGD2</field>
+ <field name="long_name">FYVE, RhoGEF and PH domain containing 2</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.1</field>
+ <field name="info">
+Glucocorticoid deficiency 2 [MIM:607398]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGD4">
+ <field name="name">FGD4</field>
+ <field name="long_name">FYVE, RhoGEF and PH domain containing 4</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p11.2</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 4H [MIM:609311]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGF10">
+ <field name="name">FGF10</field>
+ <field name="long_name">fibroblast growth factor 10</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13-p12</field>
+ <field name="info">
+Aplasia of lacrimal and salivary glands [MIM:180920]
+LADD syndrome [MIM:149730]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGF14">
+ <field name="name">FGF14</field>
+ <field name="long_name">fibroblast growth factor 14</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q34</field>
+ <field name="info">
+Spinocerebellar ataxia-27 [MIM:609307]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGF1">
+ <field name="name">FGF1</field>
+ <field name="long_name">fibroblast growth factor 1 (acidic)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGF20">
+ <field name="name">FGF20</field>
+ <field name="long_name">fibroblast growth factor 20</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p22-p21.3</field>
+ <field name="info">
+Parkinson disease, susceptibility to [MIM:168600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGF23">
+ <field name="name">FGF23</field>
+ <field name="long_name">fibroblast growth factor 23</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.3</field>
+ <field name="info">
+Hypophosphatemic rickets, autosomal dominant [MIM:193100]
+Osteomalacia, tumor-induced
+Tumoral calcinosis, hyperphosphatemic, familial [MIM:211900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGF3">
+ <field name="name">FGF3</field>
+ <field name="long_name">fibroblast growth factor 3 (murine mammary tumor virus integration site (v-int-2) oncogene homolog)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Deafness, congenital with inner ear agenesis, microtia, and microdontia [MIM:610706]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGF8">
+ <field name="name">FGF8</field>
+ <field name="long_name">fibroblast growth factor 8 (androgen-induced)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+Kallmann syndrome 6 [MIM:612702]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGF9">
+ <field name="name">FGF9</field>
+ <field name="long_name">fibroblast growth factor 9 (glia-activating factor)</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q11-q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGFR1OP">
+ <field name="name">FGFR1OP</field>
+ <field name="long_name">FGFR1 oncogene partner</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q27</field>
+ <field name="info">
+Myeloproliferative disorder</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGFR1">
+ <field name="name">FGFR1</field>
+ <field name="long_name">fibroblast growth factor receptor 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p11.2-p11.1</field>
+ <field name="info">
+Pfeiffer syndrome [MIM:101600]
+Jackson-Weiss syndrome [MIM:123150]
+Kallmann syndrome 2 [MIM:147950]
+Hypogonadotropic hypogonadism [MIM:146110]
+Osteoglophonic dysplasia [MIM:166250]
+Trigonocephaly [MIM:190440]
+Antley-Bixler syndrome [MIM:207410]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGFR2">
+ <field name="name">FGFR2</field>
+ <field name="long_name">fibroblast growth factor receptor 2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q26</field>
+ <field name="info">
+Crouzon syndrome [MIM:123500]
+Jackson-Weiss syndrome [MIM:123150]
+Beare-Stevenson cutis gyrata syndrome [MIM:123790]
+Pfeiffer syndrome [MIM:101600]
+Apert syndrome [MIM:101200]
+Saethre-Chotzen syndrome [MIM:101400]
+Craniosynostosis, nonspecific
+Gastric cancer, somatic [MIM:137215]
+Craniofacial-skeletal-dermatologic dysplasia
+Antley-Bixler syndrome [MIM:207410]
+Scaphocephaly and Axenfeld-Rieger anomaly
+LADD syndrome [MIM:149730]
+Scaphocephaly, maxillary retrusion, and mental retardation [MIM:609579]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGFR3">
+ <field name="name">FGFR3</field>
+ <field name="long_name">fibroblast growth factor receptor 3</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.3</field>
+ <field name="info">
+Achondroplasia [MIM:100800]
+Hypochondroplasia [MIM:146000]
+Thanatophoric dysplasia, types I and II [MIM:187600]
+Crouzon syndrome with acanthosis nigricans [MIM:612247]
+Muenke syndrome [MIM:602849]
+Bladder cancer [MIM:109800]
+Colorectal cancer, somatic [MIM:109800]
+Cervical cancer, somatic [MIM:603956]
+LADD syndrome [MIM:149730]
+CATSHL syndrome [MIM:610474]
+Nevus, keratinocytic, nonepidermolytic [MIM:162900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGFR4">
+ <field name="name">FGFR4</field>
+ <field name="long_name">fibroblast growth factor receptor 4</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q35.1-qter</field>
+ <field name="info">
+Cancer progression/metastasis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGFRL1">
+ <field name="name">FGFRL1</field>
+ <field name="long_name">fibroblast growth factor receptor-like 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGG">
+ <field name="name">FGG</field>
+ <field name="long_name">fibrinogen gamma chain</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q28</field>
+ <field name="info">
+Dysfibrinogenemia, gamma type
+Hypofibrinogenemia, gamma type
+Thrombophilia, dysfibrinogenemic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGS1">
+ <field name="name">FGS1</field>
+ <field name="long_name">FG syndrome 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13</field>
+ <field name="info">
+Opitz-Kaveggia syndrome [MIM:305450]
+Lujan-Fryns syndrome [MIM:309520]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGS2">
+ <field name="name">FGS2</field>
+ <field name="long_name">FG syndrome 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+FG syndrome 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGS3">
+ <field name="name">FGS3</field>
+ <field name="long_name">FG syndrome 3</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3</field>
+ <field name="info">
+FG syndrome 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FGS5">
+ <field name="name">FGS5</field>
+ <field name="long_name">FG syndrome 5</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22.3</field>
+ <field name="info">
+FG syndrome 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FHASD">
+ <field name="name">FHASD</field>
+ <field name="long_name">Foveal hypoplasia and anterior segment dysgenesis</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q23.2-q24.2</field>
+ <field name="info">
+Foveal hypoplasia and anterior segment dysgenesis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FHBL2">
+ <field name="name">FHBL2</field>
+ <field name="long_name">Hypobetalipoproteinemia, familial, 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p22-p21.1</field>
+ <field name="info">
+Hypobetalipoproteinemia, familial, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FHL1">
+ <field name="name">FHL1</field>
+ <field name="long_name">four and a half LIM domains 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q21.3-q22</field>
+ <field name="info">
+Hemophagocytic lymphohistiocytosis, familial, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FH">
+ <field name="name">FH</field>
+ <field name="long_name">fumarate hydratase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42.1</field>
+ <field name="info">
+Fumarase deficiency [MIM:606812]
+Multiple cutaneous and uterine leiomyomata [MIM:150800]
+Leiomyomatosis and renal cell cancer [MIM:605839]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FIG4">
+ <field name="name">FIG4</field>
+ <field name="long_name">FIG4 homolog (S. cerevisiae)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 4J [MIM:611228]
+Amyotrophic lateral sclerosis 11 [MIM:612577]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FIGLA">
+ <field name="name">FIGLA</field>
+ <field name="long_name">folliculogenesis specific basic helix-loop-helix</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p12</field>
+ <field name="info">
+Premature ovarian failure 6 [MIM:612310]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FIP1L1">
+ <field name="name">FIP1L1</field>
+ <field name="long_name">FIP1 like 1 (S. cerevisiae)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FKBP5">
+ <field name="name">FKBP5</field>
+ <field name="long_name">FK506 binding protein 5</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3-p21.2</field>
+ <field name="info">
+Major depressive disorder and accelerated response to antidepressant drug treatment [MIM:608516]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FKBP6">
+ <field name="name">FKBP6</field>
+ <field name="long_name">FK506 binding protein 6, 36kDa</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FKRP">
+ <field name="name">FKRP</field>
+ <field name="long_name">fukutin related protein</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+Muscular dystrophy, congenital, 1C [MIM:606612]
+Muscular dystrophy, limb-girdle, type 2I [MIM:607155]
+Muscle-eye-brain disease [MIM:253280]
+Walker-Warburg syndrome [MIM:236670]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FKTN">
+ <field name="name">FKTN</field>
+ <field name="long_name">fukutin</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q31</field>
+ <field name="info">
+Muscular dystrophy, Fukuyama congenital [MIM:253800]
+Walker-Warburg syndrome [MIM:236670]
+Cardiomyopathy, dilated, 1X [MIM:611615]
+Muscular dystrophy, limb-girdle, type 2M [MIM:611588]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FLCN">
+ <field name="name">FLCN</field>
+ <field name="long_name">folliculin</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+Birt-Hogg-Dube syndrome [MIM:135150]
+Pneumothorax, primary spontaneous [MIM:173600]
+Renal carcinoma, chromophobe, somatic [MIM:144700]
+Colorectal cancer, somatic [MIM:114500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FLG">
+ <field name="name">FLG</field>
+ <field name="long_name">filaggrin</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Ichthyosis vulgaris [MIM:146700]
+Dermatitis, atopic, susceptibility to [MIM:605803]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FLNA">
+ <field name="name">FLNA</field>
+ <field name="long_name">filamin A, alpha (actin binding protein 280)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Heterotopia, periventricular [MIM:300049]
+Otopalatodigital syndrome, type I [MIM:311300]
+Otopalatodigital syndrome, type II [MIM:304120]
+Frontometaphyseal dysplasia [MIM:304120]
+Melnick-Needles syndrome [MIM:309350]
+Heterotopia, periventricular nodular, with frontometaphyseal dysplasia [MIM:300049]
+Heterotopia, periventricular, ED variant [MIM:300537]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FLNB">
+ <field name="name">FLNB</field>
+ <field name="long_name">filamin B, beta (actin binding protein 278)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p14.3</field>
+ <field name="info">
+Spondylocarpotarsal synostosis syndrome [MIM:272460]
+Larsen syndrome [MIM:150250]
+Atelostogenesis, type I [MIM:108720]
+Atelosteogenesis, type III [MIM:108721]
+Boomerang dysplasia [MIM:112310]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FLNC">
+ <field name="name">FLNC</field>
+ <field name="long_name">filamin C, gamma (actin binding protein 280)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q32</field>
+ <field name="info">
+Myopathy, myofibrillar, filamin C-related [MIM:609524]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FLT1">
+ <field name="name">FLT1</field>
+ <field name="long_name">fms-related tyrosine kinase 1 (vascular endothelial growth factor/vascular permeability factor receptor)</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FLT3">
+ <field name="name">FLT3</field>
+ <field name="long_name">fms-related tyrosine kinase 3</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12</field>
+ <field name="info">
+Leukemia, acute myeloid, reduced survival in
+Leukemia, acute myeloid [MIM:601626]
+Leukemia, acute lymphoblastic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FLT4">
+ <field name="name">FLT4</field>
+ <field name="long_name">fms-related tyrosine kinase 4</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q35.3</field>
+ <field name="info">
+Lymphedema, hereditary I [MIM:153100]
+Hemangioma, capillary infantile, somatic [MIM:602089]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FMO1">
+ <field name="name">FMO1</field>
+ <field name="long_name">flavin containing monooxygenase 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23-q25</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FMO2">
+ <field name="name">FMO2</field>
+ <field name="long_name">flavin containing monooxygenase 2 (non-functional)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23-q25</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FMO3">
+ <field name="name">FMO3</field>
+ <field name="long_name">flavin containing monooxygenase 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23-q25</field>
+ <field name="info">
+Trimethylaminuria [MIM:602079]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FMO4">
+ <field name="name">FMO4</field>
+ <field name="long_name">flavin containing monooxygenase 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23-q25</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FMO5">
+ <field name="name">FMO5</field>
+ <field name="long_name">flavin containing monooxygenase 5</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FMR1">
+ <field name="name">FMR1</field>
+ <field name="long_name">fragile X mental retardation 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq27.3</field>
+ <field name="info">
+Fragile X syndrome [MIM:300624]
+Fragile X tremor/ataxia syndrome [MIM:300623]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FMTLE">
+ <field name="name">FMTLE</field>
+ <field name="long_name">Epilepsy, familial mesial temporal lobe</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q13.2-q21.3</field>
+ <field name="info">
+Epilepsy, familial mesial temporal lobe</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FN1">
+ <field name="name">FN1</field>
+ <field name="long_name">fibronectin 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q34</field>
+ <field name="info">
+Glomerulopathy with fibronectin deposits 2 [MIM:601894]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOLH1">
+ <field name="name">FOLH1</field>
+ <field name="long_name">folate hydrolase (prostate-specific membrane antigen) 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOLR1">
+ <field name="name">FOLR1</field>
+ <field name="long_name">folate receptor 1 (adult)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.3-q13.5</field>
+ <field name="info">
+Congenital anomalies, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOP">
+ <field name="name">FOP</field>
+ <field name="long_name">Fibrodysplasia ossificans progressiva</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p11.2-p11.1</field>
+ <field name="info">
+Pfeiffer syndrome [MIM:101600]
+Jackson-Weiss syndrome [MIM:123150]
+Kallmann syndrome 2 [MIM:147950]
+Hypogonadotropic hypogonadism [MIM:146110]
+Osteoglophonic dysplasia [MIM:166250]
+Trigonocephaly [MIM:190440]
+Antley-Bixler syndrome [MIM:207410]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXA1">
+ <field name="name">FOXA1</field>
+ <field name="long_name">forkhead box A1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXA2">
+ <field name="name">FOXA2</field>
+ <field name="long_name">forkhead box A2</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXA3">
+ <field name="name">FOXA3</field>
+ <field name="long_name">forkhead box A3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2-q13.4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXC1">
+ <field name="name">FOXC1</field>
+ <field name="long_name">forkhead box C1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p25</field>
+ <field name="info">
+Iridogoniodysgenesis, type 1 [MIM:601631]
+Rieger or Axenfeld anomalies [MIM:602482]
+Axenfeld-Rieger syndrome, type 3 [MIM:602482]
+Iris hypoplasia and glaucoma [MIM:601631]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXC2">
+ <field name="name">FOXC2</field>
+ <field name="long_name">forkhead box C2 (MFH-1, mesenchyme forkhead 1)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.3</field>
+ <field name="info">
+Lymphedema-distichiasis syndrome [MIM:153400]
+Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus [MIM:153400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXD3">
+ <field name="name">FOXD3</field>
+ <field name="long_name">forkhead box D3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+Autoimmune disease, susceptibility to, 1 [MIM:607836]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXD4">
+ <field name="name">FOXD4</field>
+ <field name="long_name">forkhead box D4</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p1-q1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXE1">
+ <field name="name">FOXE1</field>
+ <field name="long_name">forkhead box E1 (thyroid transcription factor 2)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22</field>
+ <field name="info">
+Bamforth-Lazarus syndrome [MIM:241850]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXE3">
+ <field name="name">FOXE3</field>
+ <field name="long_name">forkhead box E3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+Anterior segment mesenchymal dysgenesis [MIM:107250]
+Aphakia, congenital primary [MIM:610256]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXI1">
+ <field name="name">FOXI1</field>
+ <field name="long_name">forkhead box I1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q34</field>
+ <field name="info">
+Enlarged vestibular aqueduct [MIM:600791]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXL2">
+ <field name="name">FOXL2</field>
+ <field name="long_name">forkhead box L2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q23</field>
+ <field name="info">
+Blepharophimosis, epicanthus inversus, and ptosis, type 1 [MIM:110100]
+Blepharophimosis, epicanthus inversus, and ptosis, type 2 [MIM:110100]
+Premature ovarian failure 3 [MIM:608996]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXN1">
+ <field name="name">FOXN1</field>
+ <field name="long_name">forkhead box N1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11-q12</field>
+ <field name="info">
+T-cell immunodeficiency, congenital alopecia, and nail dystrophy [MIM:601705]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXP2">
+ <field name="name">FOXP2</field>
+ <field name="long_name">forkhead box P2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31</field>
+ <field name="info">
+Speech-language disorder-1 [MIM:602081]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FOXP3">
+ <field name="name">FOXP3</field>
+ <field name="long_name">forkhead box P3</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23-q13.3</field>
+ <field name="info">
+Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked [MIM:304790]
+Diabetes mellitus, type I, susceptibility to [MIM:222100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FPEVF">
+ <field name="name">FPEVF</field>
+ <field name="long_name">Epilepsy, partial, with variable foci</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11-q12</field>
+ <field name="info">
+Epilepsy, partial, with variable foci</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FPGS">
+ <field name="name">FPGS</field>
+ <field name="long_name">folylpolyglutamate synthase</field>
+ <field name="chromosome">9</field>
+ <field name="location">9cen-q34</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FPH">
+ <field name="name">FPH</field>
+ <field name="long_name">Hyperpigmentation, familial progressive</field>
+ <field name="chromosome">19</field>
+ <field name="location">19pter-p13.1</field>
+ <field name="info">
+Hyperpigmentation, familial progressive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FPR1">
+ <field name="name">FPR1</field>
+ <field name="long_name">formyl peptide receptor 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FRA10A">
+ <field name="name">FRA10A</field>
+ <field name="long_name">fragile site, folic acid type, rare, fra(10)(q23.3) or fra(10)(q24.2)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23.33</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FRA12A">
+ <field name="name">FRA12A</field>
+ <field name="long_name">fragile site, folic acid type, rare, fra(12)(q13.1)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13.12</field>
+ <field name="info">
+Mental retardation, FRA12A type [MIM:136630]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FRAS1">
+ <field name="name">FRAS1</field>
+ <field name="long_name">Fraser syndrome 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21</field>
+ <field name="info">
+Fraser syndrome [MIM:219000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FRAXA">
+ <field name="name">FRAXA</field>
+ <field name="long_name">fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq27.3</field>
+ <field name="info">
+Fragile X syndrome [MIM:300624]
+Fragile X tremor/ataxia syndrome [MIM:300623]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FRAXE">
+ <field name="name">FRAXE</field>
+ <field name="long_name">fragile site, folic acid type, rare, fra(X)(q28) E</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Mental retardation, X-linked, FRAXE type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FRDA2">
+ <field name="name">FRDA2</field>
+ <field name="long_name">Friedreich ataxia 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p23-p11</field>
+ <field name="info">
+Friedreich ataxia [MIM:229300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FREM2">
+ <field name="name">FREM2</field>
+ <field name="long_name">FRAS1 related extracellular matrix protein 2</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q13.3</field>
+ <field name="info">
+Fraser syndrome [MIM:219000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FRK">
+ <field name="name">FRK</field>
+ <field name="long_name">fyn-related kinase</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21-q22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FRMD7">
+ <field name="name">FRMD7</field>
+ <field name="long_name">FERM domain containing 7</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26.2</field>
+ <field name="info">
+Nystagmus 1, congenital, X-linked [MIM:310700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FRTS">
+ <field name="name">FRTS</field>
+ <field name="long_name">Fanconi renotubular syndrome</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15.3</field>
+ <field name="info">
+Fanconi renotubular syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FRZB">
+ <field name="name">FRZB</field>
+ <field name="long_name">frizzled-related protein</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31-q33</field>
+ <field name="info">
+Osteoarthritis susceptibility 1 [MIM:165720]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FSCN2">
+ <field name="name">FSCN2</field>
+ <field name="long_name">fascin homolog 2, actin-bundling protein, retinal (Strongylocentrotus purpuratus)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+Retinitis pigmentosa-30 [MIM:607921]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FSGS1">
+ <field name="name">FSGS1</field>
+ <field name="long_name">focal segmental glomerulosclerosis 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+Glomerulosclerosis, focal segmental, 1 [MIM:603278]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FSGS2">
+ <field name="name">FSGS2</field>
+ <field name="long_name">focal segmental glomerulosclerosis 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q21-q22</field>
+ <field name="info">
+Glomerulosclerosis, focal segmental, 2 [MIM:603965]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FSGS4">
+ <field name="name">FSGS4</field>
+ <field name="long_name">Focal segmental glomerulosclerosis 4</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12</field>
+ <field name="info">
+Focal segmental glomerulosclerosis 4
+End-stage renal disease, nondiabetic, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FSHB">
+ <field name="name">FSHB</field>
+ <field name="long_name">follicle stimulating hormone, beta polypeptide</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13</field>
+ <field name="info">
+Follicle-stimulating hormone deficiency, isolated [MIM:229070]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FSHMD1A">
+ <field name="name">FSHMD1A</field>
+ <field name="long_name">facioscapulohumeral muscular dystrophy 1A</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q35</field>
+ <field name="info">
+Facioscapulohumeral muscular dystrophy-1A</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FSHR">
+ <field name="name">FSHR</field>
+ <field name="long_name">follicle stimulating hormone receptor</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p21-p16</field>
+ <field name="info">
+Ovarian dysgenesis 1 [MIM:233300]
+Ovarian sex cord tumors
+Ovarian response to FSH stimulation [MIM:276400]
+Ovarian hyperstimulation syndrome [MIM:608115]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FSTL3">
+ <field name="name">FSTL3</field>
+ <field name="long_name">follistatin-like 3 (secreted glycoprotein)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13</field>
+ <field name="info">
+B cell chronic leukemia with a translocation t(11;19)(p13;q13) juxtaposing CCND1 and FSTL3 with an expression of the FSTL3 in hematopoietic cells</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FST">
+ <field name="name">FST</field>
+ <field name="long_name">follistatin</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q11.2</field>
+ <field name="info">
+Polycystic ovary syndrome [MIM:184700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FTCD">
+ <field name="name">FTCD</field>
+ <field name="long_name">formiminotransferase cyclodeaminase</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Glutamate formiminotransferase deficiency [MIM:229100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FTH1">
+ <field name="name">FTH1</field>
+ <field name="long_name">ferritin, heavy polypeptide 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q12-q13</field>
+ <field name="info">
+Iron overload, autosomal dominant</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FTL">
+ <field name="name">FTL</field>
+ <field name="long_name">ferritin, light polypeptide</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3-q13.4</field>
+ <field name="info">
+Hyperferritinemia-cataract syndrome [MIM:600886]
+Basal ganglia disease, adult-onset [MIM:606159]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FTO">
+ <field name="name">FTO</field>
+ <field name="long_name">fat mass and obesity associated</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q12.2</field>
+ <field name="info">
+Obesity, associated with [MIM:601665]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FTSJ1">
+ <field name="name">FTSJ1</field>
+ <field name="long_name">FtsJ homolog 1 (E. coli)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23</field>
+ <field name="info">
+Mental retardation, X-linked-9 [MIM:309549]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FTX">
+ <field name="name">FTX</field>
+ <field name="long_name">Thrombocytosis, familial X-linked</field>
+ <field name="chromosome">X</field>
+ <field name="location">X</field>
+ <field name="info">
+Thrombocytosis, familial X-linked</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FUCA1">
+ <field name="name">FUCA1</field>
+ <field name="long_name">fucosidase, alpha-L- 1, tissue</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34</field>
+ <field name="info">
+Fucosidosis [MIM:230000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FUS">
+ <field name="name">FUS</field>
+ <field name="long_name">fusion (involved in t(12;16) in malignant liposarcoma)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p11.2</field>
+ <field name="info">
+myxoid and round cell subtype liposarcoma,with breakpoint in t(12;16)(q13;p11) translocation</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FUT1">
+ <field name="name">FUT1</field>
+ <field name="long_name">fucosyltransferase 1 (galactoside 2-alpha-L-fucosyltransferase, H blood group)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+Bombay phenotype</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FUT2">
+ <field name="name">FUT2</field>
+ <field name="long_name">fucosyltransferase 2 (secretor status included)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+Norwalk virus infection, resistance to
+Bombay phenotype
+Vitamin B12 plasma level QTL1 [MIM:612542]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FUT3">
+ <field name="name">FUT3</field>
+ <field name="long_name">fucosyltransferase 3 (galactoside 3(4)-L-fucosyltransferase, Lewis blood group)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Blood group, Lewis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FUT6">
+ <field name="name">FUT6</field>
+ <field name="long_name">fucosyltransferase 6 (alpha (1,3) fucosyltransferase)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Fucosyltransferase-6 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FUT7">
+ <field name="name">FUT7</field>
+ <field name="long_name">fucosyltransferase 7 (alpha (1,3) fucosyltransferase)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="FXN">
+ <field name="name">FXN</field>
+ <field name="long_name">frataxin</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q13</field>
+ <field name="info">
+Friedreich ataxia [MIM:229300]
+Friedreich ataxia with retained reflexes [MIM:229300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FXYD2">
+ <field name="name">FXYD2</field>
+ <field name="long_name">FXYD domain containing ion transport regulator 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Hypomagnesemia-2, renal [MIM:154020]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FZD4">
+ <field name="name">FZD4</field>
+ <field name="long_name">frizzled homolog 4 (Drosophila)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q14-q21</field>
+ <field name="info">
+Exudative vitreoretinopathy [MIM:133780]
+Retinopathy of prematurity [MIM:133780]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="FZD9">
+ <field name="name">FZD9</field>
+ <field name="long_name">frizzled homolog 9 (Drosophila)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="G6PC2">
+ <field name="name">G6PC2</field>
+ <field name="long_name">glucose-6-phosphatase, catalytic, 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q24-q32</field>
+ <field name="info">
+Fasting plasma glucose level QTL 1 [MIM:612108]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="G6PC3">
+ <field name="name">G6PC3</field>
+ <field name="long_name">glucose 6 phosphatase, catalytic, 3</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+Neutropenia, severe congenital, autosomal recessive 4 [MIM:612541]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="G6PC">
+ <field name="name">G6PC</field>
+ <field name="long_name">glucose-6-phosphatase, catalytic subunit</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+Glycogen storage disease I</field>
+</record>
+<record model="gnuhealth.disease.gene" id="G6PD">
+ <field name="name">G6PD</field>
+ <field name="long_name">glucose-6-phosphate dehydrogenase</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+G6PD deficiency
+Favism
+Hemolytic anemia due to G6PD deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GAA">
+ <field name="name">GAA</field>
+ <field name="long_name">glucosidase, alpha; acid</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25.2-q25.3</field>
+ <field name="info">
+Glycogen storage disease II [MIM:232300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GAB2">
+ <field name="name">GAB2</field>
+ <field name="long_name">GRB2-associated binding protein 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.4-q13.5</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GABBR2">
+ <field name="name">GABBR2</field>
+ <field name="long_name">gamma-aminobutyric acid (GABA) B receptor, 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22.1</field>
+ <field name="info">
+Nicotine dependence, susceptibility to [MIM:188890]
+Nicotine dependence, protection against [MIM:188890]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GABRA1">
+ <field name="name">GABRA1</field>
+ <field name="long_name">gamma-aminobutyric acid (GABA) A receptor, alpha 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q34-q35</field>
+ <field name="info">
+Epilepsy, juvenile myoclonic [MIM:606904]
+Epilepsy, childhood absence, 4 [MIM:611136]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GABRA2">
+ <field name="name">GABRA2</field>
+ <field name="long_name">gamma-aminobutyric acid (GABA) A receptor, alpha 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p13-p12</field>
+ <field name="info">
+Alcoholism, susceptibility to [MIM:103780]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GABRB3">
+ <field name="name">GABRB3</field>
+ <field name="long_name">gamma-aminobutyric acid (GABA) A receptor, beta 3</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q11.2-q12</field>
+ <field name="info">
+Insomnia
+Epilepsy, childhood absence, 5 [MIM:612269]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GABRD">
+ <field name="name">GABRD</field>
+ <field name="long_name">gamma-aminobutyric acid (GABA) A receptor, delta</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GABRG2">
+ <field name="name">GABRG2</field>
+ <field name="long_name">gamma-aminobutyric acid (GABA) A receptor, gamma 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1-q33.1</field>
+ <field name="info">
+Epilepsy, generalized, with febrile seizures plus, type 3 [MIM:604233]
+Epilepsy, childhood absence, 2 [MIM:607681]
+Febrile convulsions, familial, 8 [MIM:611277]
+Myoclonic epilepsy, severe, of infancy [MIM:607208]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GAD1">
+ <field name="name">GAD1</field>
+ <field name="long_name">glutamate decarboxylase 1 (brain, 67kDa)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31</field>
+ <field name="info">
+Cerebral palsy, spastic, symmetric, autosomal recessive [MIM:603513]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GAD2">
+ <field name="name">GAD2</field>
+ <field name="long_name">glutamate decarboxylase 2 (pancreatic islets and brain, 65kDa)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p11.23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GALC">
+ <field name="name">GALC</field>
+ <field name="long_name">galactosylceramidase</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q31</field>
+ <field name="info">
+Krabbe disease [MIM:245200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GALE">
+ <field name="name">GALE</field>
+ <field name="long_name">UDP-galactose-4-epimerase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36-p35</field>
+ <field name="info">
+Galactose epimerase deficiency [MIM:230350]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GALK1">
+ <field name="name">GALK1</field>
+ <field name="long_name">galactokinase 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q24</field>
+ <field name="info">
+Galactokinase deficiency with cataracts [MIM:230200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GALNS">
+ <field name="name">GALNS</field>
+ <field name="long_name">galactosamine (N-acetyl)-6-sulfate sulfatase</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.3</field>
+ <field name="info">
+Mucopolysaccharidosis IVA [MIM:253000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GALNT3">
+ <field name="name">GALNT3</field>
+ <field name="long_name">UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 3 (GalNAc-T3)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q24-q31</field>
+ <field name="info">
+Tumoral calcinosis, hyperphosphatemic, familial [MIM:211900]
+Hyperostosis-hyperphosphatemia syndrome [MIM:610233]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GALT">
+ <field name="name">GALT</field>
+ <field name="long_name">galactose-1-phosphate uridylyltransferase</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p13</field>
+ <field name="info">
+Galactosemia [MIM:230400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GAMT">
+ <field name="name">GAMT</field>
+ <field name="long_name">guanidinoacetate N-methyltransferase</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+GAMT deficiency [MIM:612736]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GAN">
+ <field name="name">GAN</field>
+ <field name="long_name">gigaxonin</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.1</field>
+ <field name="info">
+Giant axonal neuropathy-1 [MIM:256850]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GARS">
+ <field name="name">GARS</field>
+ <field name="long_name">glycyl-tRNA synthetase</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 2D [MIM:601472]
+Neuropathy, distal hereditary motor, type V [MIM:600794]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GATA1">
+ <field name="name">GATA1</field>
+ <field name="long_name">GATA binding protein 1 (globin transcription factor 1)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23</field>
+ <field name="info">
+Dyserythropoietic anemia with thrombocytopenia [MIM:300367]
+Macrothrombocytopenia [MIM:300367]
+Leukemia, megakaryoblastic, with or without Down syndrome [MIM:190685]
+Leukemia, megakaryoblastic, of Down syndrome [MIM:190685]
+Thrombocytopenia with beta-thalassemia, X-linked [MIM:314050]
+Anemia, X-linked, without thrombocytopenia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GATA2">
+ <field name="name">GATA2</field>
+ <field name="long_name">GATA binding protein 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GATA3">
+ <field name="name">GATA3</field>
+ <field name="long_name">GATA binding protein 3</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p15</field>
+ <field name="info">
+Hypoparathyroidism, sensorineural deafness, and renal dysplasia [MIM:146255]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GATA4">
+ <field name="name">GATA4</field>
+ <field name="long_name">GATA binding protein 4</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23.1-p22</field>
+ <field name="info">
+Atrial septal defect-2 [MIM:607941]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GATM">
+ <field name="name">GATM</field>
+ <field name="long_name">glycine amidinotransferase (L-arginine:glycine amidinotransferase)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15.3</field>
+ <field name="info">
+AGAT deficiency [MIM:612718]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GBA3">
+ <field name="name">GBA3</field>
+ <field name="long_name">glucosidase, beta, acid 3 (cytosolic)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15.31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GBAP">
+ <field name="name">GBAP</field>
+ <field name="long_name">glucosidase, beta; acid, pseudogene</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Gaucher disease, type I [MIM:230800]
+Gaucher disease, type II [MIM:230900]
+Gaucher disease, type III [MIM:231000]
+Gaucher disease, type IIIC [MIM:231005]
+Gaucher disease, perinatal lethal [MIM:608013]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GBA">
+ <field name="name">GBA</field>
+ <field name="long_name">glucosidase, beta; acid (includes glucosylceramidase)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Gaucher disease, type I [MIM:230800]
+Gaucher disease, type II [MIM:230900]
+Gaucher disease, type III [MIM:231000]
+Gaucher disease, type IIIC [MIM:231005]
+Gaucher disease, perinatal lethal [MIM:608013]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GBE1">
+ <field name="name">GBE1</field>
+ <field name="long_name">glucan (1,4-alpha-), branching enzyme 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p12</field>
+ <field name="info">
+Glycogen storage disease IV [MIM:232500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GCCD2">
+ <field name="name">GCCD2</field>
+ <field name="long_name">Glucocorticoid deficiency 2</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.1</field>
+ <field name="info">
+Glucocorticoid deficiency 2 [MIM:607398]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GCDH">
+ <field name="name">GCDH</field>
+ <field name="long_name">glutaryl-Coenzyme A dehydrogenase</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2</field>
+ <field name="info">
+Glutaricaciduria, type I [MIM:231670]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GCGR">
+ <field name="name">GCGR</field>
+ <field name="long_name">glucagon receptor</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GCG">
+ <field name="name">GCG</field>
+ <field name="long_name">glucagon</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q36-q37</field>
+ <field name="info">
+Hyperproglucagonemia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GCH1">
+ <field name="name">GCH1</field>
+ <field name="long_name">GTP cyclohydrolase 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q22.1-q22.2</field>
+ <field name="info">
+Dystonia, DOPA-responsive, with or without hyperphenylalainemia [MIM:233910]
+Hyperpehnylalaninemia, BH4-deficient, B [MIM:233910]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GCKR">
+ <field name="name">GCKR</field>
+ <field name="long_name">glucokinase (hexokinase 4) regulator</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p23.3-p23.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GCK">
+ <field name="name">GCK</field>
+ <field name="long_name">glucokinase (hexokinase 4)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15-p13</field>
+ <field name="info">
+MODY, type II [MIM:125851]
+Diabetes mellitus, noninsulin-dependent, late onset [MIM:125853]
+Diabetes mellitus, gestational [MIM:125851]
+Hyperinsulinemic hypoglycemia, familial, 3 [MIM:602485]
+Diabetes mellitus, permanent neonatal [MIM:606176]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GCLC">
+ <field name="name">GCLC</field>
+ <field name="long_name">glutamate-cysteine ligase, catalytic subunit</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12</field>
+ <field name="info">
+Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency [MIM:230450]
+Myocardial infarction, susceptibility to [MIM:608446]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GCLM">
+ <field name="name">GCLM</field>
+ <field name="long_name">glutamate-cysteine ligase, modifier subunit</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p22.1</field>
+ <field name="info">
+Myocardial infarction, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GCNT2">
+ <field name="name">GCNT2</field>
+ <field name="long_name">glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p24-p23</field>
+ <field name="info">
+Blood group, Ii [MIM:110800]
+Adult i phenotype with congenital cataract [MIM:110800]
+Adult i phenotype without cataract [MIM:110800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GCSH">
+ <field name="name">GCSH</field>
+ <field name="long_name">glycine cleavage system protein H (aminomethyl carrier)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24</field>
+ <field name="info">
+Glycine encephalopathy [MIM:605899]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GC">
+ <field name="name">GC</field>
+ <field name="long_name">group-specific component (vitamin D binding protein)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q12</field>
+ <field name="info">
+Graves disease, susceptibility to, 3 [MIM:275000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GDAP1">
+ <field name="name">GDAP1</field>
+ <field name="long_name">ganglioside-induced differentiation-associated protein 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q13-q21.1</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 4A [MIM:214400]
+Charcot-Marie-Tooth disease, axonal, with vocal cord paresis [MIM:607706]
+Charcot-Marie-Tooth disease, axonal, type 2K [MIM:607831]
+Charcot-Marie-Tooth disease, recessive intermediate A [MIM:608340]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GDB2">
+ <field name="name">GDB2</field>
+ <field name="long_name">Gallbladder disease 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.21</field>
+ <field name="info">
+Gallbladder disease 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GDF1">
+ <field name="name">GDF1</field>
+ <field name="long_name">growth differentiation factor 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p12</field>
+ <field name="info">
+Transposition of great arteries, dextro-looped 3
+Double-outlet right ventricle [MIM:217095]
+Tetralogy of Fallot [MIM:187500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GDF5">
+ <field name="name">GDF5</field>
+ <field name="long_name">growth differentiation factor 5</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11.2</field>
+ <field name="info">
+Acromesomelic dysplasia, Hunter-Thompson type [MIM:201250]
+Brachydactyly, type C [MIM:113100]
+Chondrodysplasia, Grebe type [MIM:200700]
+Fibular hypoplasia and complex brachydactyly [MIM:228900]
+Brachydactyly, type A2 [MIM:112600]
+Symphalangism, proximal [MIM:185800]
+Multiple synostoses syndrome type 1 [MIM:610017]
+Osteoarthritis [MIM:612400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GDF6">
+ <field name="name">GDF6</field>
+ <field name="long_name">growth differentiation factor 6</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q22.1</field>
+ <field name="info">
+Ocular coloboma [MIM:120200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GDI1">
+ <field name="name">GDI1</field>
+ <field name="long_name">GDP dissociation inhibitor 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Mental retardation, X-linked nonspecific [MIM:309541]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GDNF">
+ <field name="name">GDNF</field>
+ <field name="long_name">glial cell derived neurotrophic factor</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13.1-p12</field>
+ <field name="info">
+Hirschsprung disease [MIM:142623]
+Central hypoventilation syndrome [MIM:209880]
+Pheochromocytoma, modifier of [MIM:171300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GDXYM">
+ <field name="name">GDXYM</field>
+ <field name="long_name">Gonadal dysgenesis, XY type</field>
+ <field name="chromosome">5</field>
+ <field name="location">5cen</field>
+ <field name="info">
+Gonadal dysgenesis, XY type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GDXY">
+ <field name="name">GDXY</field>
+ <field name="long_name">gonadal dysgenesis, XY female type</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.11-p21.2</field>
+ <field name="info">
+Gonadal dysgenesis, XY female type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GEFSP4">
+ <field name="name">GEFSP4</field>
+ <field name="long_name">Epilepsy, generalized, with febrile seizures plus, type 4</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p24</field>
+ <field name="info">
+Epilepsy, generalized, with febrile seizures plus, type 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GEFSP6">
+ <field name="name">GEFSP6</field>
+ <field name="long_name">Generalized epilepsy with febrile seizures plus, type 6</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23-p21</field>
+ <field name="info">
+Generalized epilepsy with febrile seizures plus, type 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GEM">
+ <field name="name">GEM</field>
+ <field name="long_name">GTP binding protein overexpressed in skeletal muscle</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q13-q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GER">
+ <field name="name">GER</field>
+ <field name="long_name">Gastroesophageal reflux</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14</field>
+ <field name="info">
+Gastroesophageal reflux</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GEVQ1">
+ <field name="name">GEVQ1</field>
+ <field name="long_name">gene expression, variation in, quantitative trait locus</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32</field>
+ <field name="info">
+Gene expression, variation in, QTL</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GEVQ2">
+ <field name="name">GEVQ2</field>
+ <field name="long_name">gene expression, variation in, quantitative trait locus</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13</field>
+ <field name="info">
+Gene expression, variation in, QTL</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GFAP">
+ <field name="name">GFAP</field>
+ <field name="long_name">glial fibrillary acidic protein</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+Alexander disease [MIM:203450]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GFI1">
+ <field name="name">GFI1</field>
+ <field name="long_name">growth factor independent 1 transcription repressor</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p22</field>
+ <field name="info">
+Neutropenia, severe congenital [MIM:202700]
+Neutropenia, nonimmune chronic idiopathic, of adults [MIM:607847]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GFM1">
+ <field name="name">GFM1</field>
+ <field name="long_name">G elongation factor, mitochondrial 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q25.1-q26.2</field>
+ <field name="info">
+Combined oxidative phosphorylation deficiency 1 [MIM:609060]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GFPT2">
+ <field name="name">GFPT2</field>
+ <field name="long_name">glutamine-fructose-6-phosphate transaminase 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q34-q35</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GFRA1">
+ <field name="name">GFRA1</field>
+ <field name="long_name">GDNF family receptor alpha 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q26</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GGCX">
+ <field name="name">GGCX</field>
+ <field name="long_name">gamma-glutamyl carboxylase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p12</field>
+ <field name="info">
+Vitamin K-dependent coagulation defect [MIM:277450]
+Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency [MIM:610842]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GGH">
+ <field name="name">GGH</field>
+ <field name="long_name">gamma-glutamyl hydrolase (conjugase, folylpolygammaglutamyl hydrolase)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q12.2-q13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GGT1">
+ <field name="name">GGT1</field>
+ <field name="long_name">gamma-glutamyltransferase 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.1-q11.2</field>
+ <field name="info">
+Glutathioninuria</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GGT2">
+ <field name="name">GGT2</field>
+ <field name="long_name">gamma-glutamyltransferase 2</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.1</field>
+ <field name="info">
+Gamma-glutamyltransferase, familial high serum</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GGT6">
+ <field name="name">GGT6</field>
+ <field name="long_name">gamma-glutamyltransferase 6</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.2</field>
+ <field name="info">
+glutathionuria</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GH1">
+ <field name="name">GH1</field>
+ <field name="long_name">growth hormone 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q22-q24</field>
+ <field name="info">
+Growth hormone deficiency
+Growth hormone deficiency, isolated, type IA [MIM:262400]
+Growth hormone deficiency, isolated, type IB [MIM:262400]
+Growth hormone deficiency, isolated, type II [MIM:173100]
+Kowarski syndrome [MIM:262650]
+Short stature, familial [MIM:604271]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GH2">
+ <field name="name">GH2</field>
+ <field name="long_name">growth hormone 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q22-q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GHRHR">
+ <field name="name">GHRHR</field>
+ <field name="long_name">growth hormone releasing hormone receptor</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15-p14</field>
+ <field name="info">
+Growth hormone deficient dwarfism</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GHRH">
+ <field name="name">GHRH</field>
+ <field name="long_name">growth hormone releasing hormone</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11.2</field>
+ <field name="info">
+Isolated growth hormone deficiency due to defect in GHRF
+Gigantism due to GHRF hypersecretion</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GHRL">
+ <field name="name">GHRL</field>
+ <field name="long_name">ghrelin/obestatin prepropeptide</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26-p25</field>
+ <field name="info">
+Obesity, susceptibility to [MIM:601665]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GHR">
+ <field name="name">GHR</field>
+ <field name="long_name">growth hormone receptor</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13-p12</field>
+ <field name="info">
+Laron dwarfism [MIM:262500]
+Short stature, idiopathic
+Short stature, autosomal dominant, with normal serum growth hormone binding protein
+Increased responsiveness to growth hormone</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GHSR">
+ <field name="name">GHSR</field>
+ <field name="long_name">growth hormone secretagogue receptor</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.3</field>
+ <field name="info">
+Short stature [MIM:604271]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GIF">
+ <field name="name">GIF</field>
+ <field name="long_name">gastric intrinsic factor (vitamin B synthesis)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Intrinsic factor deficiency [MIM:261000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GIGYF2">
+ <field name="name">GIGYF2</field>
+ <field name="long_name">GRB10 interacting GYF protein 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.1</field>
+ <field name="info">
+Parkinson disease 11 [MIM:607688]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GINGF2">
+ <field name="name">GINGF2</field>
+ <field name="long_name">gingival fibromatosis, hereditary, 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13-q22</field>
+ <field name="info">
+Fibromatosis, gingival, 2 [MIM:135300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GINGF3">
+ <field name="name">GINGF3</field>
+ <field name="long_name">Fibromatosis, gingival, 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p23.3-p22.3</field>
+ <field name="info">
+Fibromatosis, gingival, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GINGF4">
+ <field name="name">GINGF4</field>
+ <field name="long_name">Fibromatosis, gingival, 4</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15</field>
+ <field name="info">
+Fibromatosis, gingival, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GIPR">
+ <field name="name">GIPR</field>
+ <field name="long_name">gastric inhibitory polypeptide receptor</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GJA1">
+ <field name="name">GJA1</field>
+ <field name="long_name">gap junction protein, alpha 1, 43kDa</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21-q23.2</field>
+ <field name="info">
+Oculodentodigital dysplasia [MIM:164200]
+Syndactyly, type III [MIM:186100]
+Hypoplastic left heart syndrome [MIM:241550]
+Atrioventricular septal defect [MIM:600309]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GJA3">
+ <field name="name">GJA3</field>
+ <field name="long_name">gap junction protein, alpha 3, 46kDa</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q11</field>
+ <field name="info">
+Cataract, zonular pulverulent-3 [MIM:601885]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GJA4">
+ <field name="name">GJA4</field>
+ <field name="long_name">gap junction protein, alpha 4, 37kDa</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p35.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GJA5">
+ <field name="name">GJA5</field>
+ <field name="long_name">gap junction protein, alpha 5, 40kDa</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21.1</field>
+ <field name="info">
+Atrial fibrillation [MIM:608583]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GJA8">
+ <field name="name">GJA8</field>
+ <field name="long_name">gap junction protein, alpha 8, 50kDa</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21.1</field>
+ <field name="info">
+Cataract, zonular pulverulent-1 [MIM:116200]
+Cataract, nuclear progressive
+Cataract-microcornea syndrome [MIM:116150]
+Cataract, nuclear pulverulent</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GJB1">
+ <field name="name">GJB1</field>
+ <field name="long_name">gap junction protein, beta 1, 32kDa</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.1</field>
+ <field name="info">
+Charcot-Marie-Tooth neuropathy, X-linked dominant, 1 [MIM:302800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GJB2">
+ <field name="name">GJB2</field>
+ <field name="long_name">gap junction protein, beta 2, 26kDa</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q11-q12</field>
+ <field name="info">
+Deafness, autosomal recessive 1A [MIM:220290]
+Deafness, autosomal dominant 3A [MIM:601544]
+Vohwinkel syndrome [MIM:124500]
+Keratoderma, palmoplantar, with deafness [MIM:148350]
+Keratitis-ichthyosis-deafness syndrome [MIM:148210]
+Hystrix-like ichthyosis with deafness [MIM:602540]
+Bart-Pumphrey syndrome [MIM:149200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GJB3">
+ <field name="name">GJB3</field>
+ <field name="long_name">gap junction protein, beta 3, 31kDa</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p35.1</field>
+ <field name="info">
+Erythrokeratodermia variabilis [MIM:133200]
+Deafness, autosomal dominant 2B [MIM:612644]
+Deafness, autosomal recessive
+Deafness, autosomal dominant, with peripheral neuropathy
+Deafness, digenic, GJB2/GJB3 [MIM:220290]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GJB4">
+ <field name="name">GJB4</field>
+ <field name="long_name">gap junction protein, beta 4, 30.3kDa</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p35.1</field>
+ <field name="info">
+Erythrokeratodermia variabilis with erythema gyratum repens [MIM:133200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GJB6">
+ <field name="name">GJB6</field>
+ <field name="long_name">gap junction protein, beta 6, 30kDa</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12</field>
+ <field name="info">
+Deafness, autosomal dominant 3B [MIM:612643]
+Ectodermal dysplasia, hidrotic [MIM:129500]
+Deafness, autosomal recessive 1B [MIM:612645]
+Deafness, digenic GJB2/GJB6 [MIM:220290]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GJC2">
+ <field name="name">GJC2</field>
+ <field name="long_name">gap junction protein, gamma 2, 47kDa</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q41-q42</field>
+ <field name="info">
+Leukodystrophy, hypomyelinating, 2 [MIM:608804]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GJD2">
+ <field name="name">GJD2</field>
+ <field name="long_name">gap junction protein, delta 2, 36kDa</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GK">
+ <field name="name">GK</field>
+ <field name="long_name">glycerol kinase</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp21.3-p21.2</field>
+ <field name="info">
+Glycerol kinase deficiency [MIM:307030]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLA">
+ <field name="name">GLA</field>
+ <field name="long_name">galactosidase, alpha</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22</field>
+ <field name="info">
+Fabry disease [MIM:301500]
+Fabry disease, cardiac variant [MIM:301500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLB1">
+ <field name="name">GLB1</field>
+ <field name="long_name">galactosidase, beta 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.33</field>
+ <field name="info">
+GM1-gangliosidosis, type I [MIM:230500]
+GM1-gangliosidosis, type II [MIM:230600]
+GM1-gangliosidosis, type III [MIM:230650]
+Morquio syndrome B [MIM:253010]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLC1B">
+ <field name="name">GLC1B</field>
+ <field name="long_name">glaucoma 1, open angle, B (adult-onset)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2cen-q13</field>
+ <field name="info">
+Glaucoma 1B, primary open angle, adult onset [MIM:137760]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLC1C">
+ <field name="name">GLC1C</field>
+ <field name="long_name">glaucoma 1, open angle, C</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21-q24</field>
+ <field name="info">
+Glaucoma 1C, primary open angle</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLC1D">
+ <field name="name">GLC1D</field>
+ <field name="long_name">glaucoma 1, open angle, D (adult-onset)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q23</field>
+ <field name="info">
+Glaucoma 1D, primary open angle</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLC1F">
+ <field name="name">GLC1F</field>
+ <field name="long_name">glaucoma 1, open angle, F (adult-onset)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q35-q36</field>
+ <field name="info">
+Glaucoma 1F</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLC1I">
+ <field name="name">GLC1I</field>
+ <field name="long_name">glaucoma 1, open angle, I</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q11-q13</field>
+ <field name="info">
+Glaucoma 1, open angle, I</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLC1K">
+ <field name="name">GLC1K</field>
+ <field name="long_name">glaucoma 1, open angle, K (juvenile-onset)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p12</field>
+ <field name="info">
+Glaucoma 1K, primary open angle, juvenile-onset</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLC1M">
+ <field name="name">GLC1M</field>
+ <field name="long_name">glaucoma 1, open angle, M (juvenile-onset)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q22.1-q32</field>
+ <field name="info">
+Glaucoma 1, open angle, M</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLC3B">
+ <field name="name">GLC3B</field>
+ <field name="long_name">glaucoma 3, primary infantile, B</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2-p36.1</field>
+ <field name="info">
+Glaucoma 3, primary infantile, B</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLDC">
+ <field name="name">GLDC</field>
+ <field name="long_name">glycine dehydrogenase (decarboxylating)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p22</field>
+ <field name="info">
+Glycine encephalopathy [MIM:605899]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLE1">
+ <field name="name">GLE1</field>
+ <field name="long_name">GLE1 RNA export mediator homolog (yeast)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+Lethal congenital contracture syndrome 1 [MIM:253310]
+Arthrogryposis, lethal, with anterior horn cell disease [MIM:611890]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLI2">
+ <field name="name">GLI2</field>
+ <field name="long_name">GLI family zinc finger 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14</field>
+ <field name="info">
+Pituitary anomalies with holoprosencephaly-like features
+Holoprosencephaly-9 [MIM:610829]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLI3">
+ <field name="name">GLI3</field>
+ <field name="long_name">GLI family zinc finger 3</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p13</field>
+ <field name="info">
+Greig cephalopolysyndactyly syndrome [MIM:175700]
+Pallister-Hall syndrome [MIM:146510]
+Polydactyly, preaxial, type IV [MIM:174700]
+Polydactyly, postaxial, types A1 and B [MIM:174200]
+Acrocallosal syndrome [MIM:200990]
+Hypothalamic hamartomas, somatic [MIM:241800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLIS2">
+ <field name="name">GLIS2</field>
+ <field name="long_name">GLIS family zinc finger 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+Nephronophthisis 7 [MIM:611498]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLIS3">
+ <field name="name">GLIS3</field>
+ <field name="long_name">GLIS family zinc finger 3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p24.3-p23</field>
+ <field name="info">
+Diabetes mellitus, neonatal, with congenital hypothyroidism [MIM:610199]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLM1">
+ <field name="name">GLM1</field>
+ <field name="long_name">Glioma, familial, 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q23-q26.3</field>
+ <field name="info">
+Glioma of brain [MIM:137800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLO1">
+ <field name="name">GLO1</field>
+ <field name="long_name">glyoxalase I</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3-p21.2</field>
+ <field name="info">
+Autism, susceptibility to [MIM:209850]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLP1R">
+ <field name="name">GLP1R</field>
+ <field name="long_name">glucagon-like peptide 1 receptor</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLRA1">
+ <field name="name">GLRA1</field>
+ <field name="long_name">glycine receptor, alpha 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q32</field>
+ <field name="info">
+Startle disease/hyperekplexia, autosomal dominant [MIM:149400]
+Startle disease, autosomal recessive
+Hyperekplexia and spastic paraparesis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLRB">
+ <field name="name">GLRB</field>
+ <field name="long_name">glycine receptor, beta</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q31.3</field>
+ <field name="info">
+Hyperekplexia, autosomal recessive [MIM:149400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLRX5">
+ <field name="name">GLRX5</field>
+ <field name="long_name">glutaredoxin 5</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32</field>
+ <field name="info">
+Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive [MIM:205950]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLTSCR1">
+ <field name="name">GLTSCR1</field>
+ <field name="long_name">glioma tumor suppressor candidate region gene 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLUD1">
+ <field name="name">GLUD1</field>
+ <field name="long_name">glutamate dehydrogenase 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23.3</field>
+ <field name="info">
+Hyperinsulinism-hyperammonemia syndrome [MIM:606762]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GLUL">
+ <field name="name">GLUL</field>
+ <field name="long_name">glutamate-ammonia ligase (glutamine synthetase)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31</field>
+ <field name="info">
+Glutamine deficiency, congenital [MIM:610015]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GM2A">
+ <field name="name">GM2A</field>
+ <field name="long_name">GM2 ganglioside activator</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.3-q33.1</field>
+ <field name="info">
+GM2-gangliosidosis, AB variant</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GMIP">
+ <field name="name">GMIP</field>
+ <field name="long_name">GEM interacting protein</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p12-p11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GMPS">
+ <field name="name">GMPS</field>
+ <field name="long_name">guanine monphosphate synthetase</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q24</field>
+ <field name="info">
+Leukemia, acute myelogenous [MIM:601626]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNAI2">
+ <field name="name">GNAI2</field>
+ <field name="long_name">guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21</field>
+ <field name="info">
+Pituitary ACTH-secreting adenoma
+Ventricular tachycardia, idiopathic [MIM:192605]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNAQ">
+ <field name="name">GNAQ</field>
+ <field name="long_name">guanine nucleotide binding protein (G protein), q polypeptide</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q21</field>
+ <field name="info">
+Bleeding diathesis due to GNAQ deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNASAS">
+ <field name="name">GNASAS</field>
+ <field name="long_name">GNAS antisense RNA (non-protein coding)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.2</field>
+ <field name="info">
+Pseudohypoparathyroidism, type IB [MIM:603233]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNAS">
+ <field name="name">GNAS</field>
+ <field name="long_name">GNAS complex locus</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.2</field>
+ <field name="info">
+Pseudohypoparathyroidism Ia [MIM:103580]
+McCune-Albright syndrome [MIM:174800]
+Pituitary ACTH secreting adenoma, somatic [MIM:219090]
+Osseous heteroplasia, progressive [MIM:166350]
+Pseudohypoparathyroidism Ib [MIM:603233]
+Prolonged bleeding time, brachydactyly and mental retardation
+Acromegaly [MIM:102200]
+Pseudopseudohypoparathyroidism [MIM:612463]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNAT1">
+ <field name="name">GNAT1</field>
+ <field name="long_name">guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21</field>
+ <field name="info">
+Night blindness, congenital stationary</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNAT2">
+ <field name="name">GNAT2</field>
+ <field name="long_name">guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13</field>
+ <field name="info">
+Achromatopsia-4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNB1L">
+ <field name="name">GNB1L</field>
+ <field name="long_name">guanine nucleotide binding protein (G protein), beta polypeptide 1-like</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNB3">
+ <field name="name">GNB3</field>
+ <field name="long_name">guanine nucleotide binding protein (G protein), beta polypeptide 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+Hypertension, essential, susceptibility to [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNE">
+ <field name="name">GNE</field>
+ <field name="long_name">glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p13.3</field>
+ <field name="info">
+Sialuria [MIM:269921]
+Inclusion body myopathy, autosomal recessive [MIM:600737]
+Nonaka myopathy [MIM:605820]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNMT">
+ <field name="name">GNMT</field>
+ <field name="long_name">glycine N-methyltransferase</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12</field>
+ <field name="info">
+Glycine N-methyltransferase deficiency [MIM:606664]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNPAT">
+ <field name="name">GNPAT</field>
+ <field name="long_name">glyceronephosphate O-acyltransferase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42</field>
+ <field name="info">
+Chondrodysplasia punctata, rhizomelic, type 2 [MIM:222765]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNPTAB">
+ <field name="name">GNPTAB</field>
+ <field name="long_name">N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q23.3</field>
+ <field name="info">
+Mucolipidosis III alpha/beta [MIM:252600]
+Mucolipidosis II alpha/beta [MIM:252500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNRH1">
+ <field name="name">GNRH1</field>
+ <field name="long_name">gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21-p11.2</field>
+ <field name="info">
+Hypogonadotropic hypogonadism due to GNRH deficiency [MIM:227200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNRHR">
+ <field name="name">GNRHR</field>
+ <field name="long_name">gonadotropin-releasing hormone receptor</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21.2</field>
+ <field name="info">
+Hypogonadotropic hypogonadism
+Fertile eunuch syndrome [MIM:228300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GNS">
+ <field name="name">GNS</field>
+ <field name="long_name">glucosamine (N-acetyl)-6-sulfatase</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q14</field>
+ <field name="info">
+Mucopolysaccharidosis type IIID [MIM:252940]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GOA1">
+ <field name="name">GOA1</field>
+ <field name="long_name">Osteoarthritis, generalized, without dysplasia, susceptibility to</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33.3</field>
+ <field name="info">
+Osteoarthritis susceptibility 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GOLGA5">
+ <field name="name">GOLGA5</field>
+ <field name="long_name">golgi autoantigen, golgin subfamily a, 5</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q</field>
+ <field name="info">
+Thyroid carcinoma, papillary [MIM:188550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GOPC">
+ <field name="name">GOPC</field>
+ <field name="long_name">golgi associated PDZ and coiled-coil motif containing</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+Globozoospermia [MIM:102530]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GOUT1">
+ <field name="name">GOUT1</field>
+ <field name="long_name">gout susceptibility 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q25</field>
+ <field name="info">
+Gout, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GP1BA">
+ <field name="name">GP1BA</field>
+ <field name="long_name">glycoprotein Ib (platelet), alpha polypeptide</field>
+ <field name="chromosome">17</field>
+ <field name="location">17pter-p12</field>
+ <field name="info">
+Bernard-Soulier syndrome, type A [MIM:231200]
+von Willebrand disease, platelet-type [MIM:177820]
+Nonarteritic anterior ischemic optic neuropathy, susceptibility to [MIM:258660]
+Bernard-Soulier syndrome, benign autosomal dominant [MIM:153670]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GP1BB">
+ <field name="name">GP1BB</field>
+ <field name="long_name">glycoprotein Ib (platelet), beta polypeptide</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+Bernard-Soulier syndrome, type B [MIM:231200]
+Giant platelet disorder, isolated</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GP6">
+ <field name="name">GP6</field>
+ <field name="long_name">glycoprotein VI (platelet)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GP9">
+ <field name="name">GP9</field>
+ <field name="long_name">glycoprotein IX (platelet)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21</field>
+ <field name="info">
+Bernard-Soulier syndrome, type C [MIM:231200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPAM">
+ <field name="name">GPAM</field>
+ <field name="long_name">glycerol-3-phosphate acyltransferase, mitochondrial</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24-q26</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPC3">
+ <field name="name">GPC3</field>
+ <field name="long_name">glypican 3</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26</field>
+ <field name="info">
+Simpson-Golabi-Behmel syndrome, type 1 [MIM:312870]
+Wilms tumor, somatic [MIM:194070]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPD1L">
+ <field name="name">GPD1L</field>
+ <field name="long_name">glycerol-3-phosphate dehydrogenase 1-like</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p22.3</field>
+ <field name="info">
+Brugada syndrome 2 [MIM:611777]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPD2">
+ <field name="name">GPD2</field>
+ <field name="long_name">glycerol-3-phosphate dehydrogenase 2 (mitochondrial)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q24.1</field>
+ <field name="info">
+Diabetes, type 2, susceptibility to [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPDS1">
+ <field name="name">GPDS1</field>
+ <field name="long_name">glaucoma-related pigment dispersion syndrome 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q35-q36</field>
+ <field name="info">
+Pigment dispersion syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPIHBP1">
+ <field name="name">GPIHBP1</field>
+ <field name="long_name">glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPI">
+ <field name="name">GPI</field>
+ <field name="long_name">glucose phosphate isomerase</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+Hemolytic anemia due to glucosephosphate isomerase deficiency
+Hydrops fetalis, one form</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPR143">
+ <field name="name">GPR143</field>
+ <field name="long_name">G protein-coupled receptor 143</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3</field>
+ <field name="info">
+Ocular albinism, Nettleship-Falls type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPR44">
+ <field name="name">GPR44</field>
+ <field name="long_name">G protein-coupled receptor 44</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q12-q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPR56">
+ <field name="name">GPR56</field>
+ <field name="long_name">G protein-coupled receptor 56</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q13</field>
+ <field name="info">
+Polymicrogyria, bilateral frontoparietal [MIM:606854]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPR68">
+ <field name="name">GPR68</field>
+ <field name="long_name">G protein-coupled receptor 68</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPR98">
+ <field name="name">GPR98</field>
+ <field name="long_name">G protein-coupled receptor 98</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q14</field>
+ <field name="info">
+Convulsions, familial febrile, 4 [MIM:604352]
+Usher syndrome, type IIC [MIM:605472]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPSC">
+ <field name="name">GPSC</field>
+ <field name="long_name">gliosis, familial progressive subcortical</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+Gliosis, familial progressive subcortical</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPX1">
+ <field name="name">GPX1</field>
+ <field name="long_name">glutathione peroxidase 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.3</field>
+ <field name="info">
+Hemolytic anemia due to glutathione peroxidase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GPX4">
+ <field name="name">GPX4</field>
+ <field name="long_name">glutathione peroxidase 4 (phospholipid hydroperoxidase)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRB10">
+ <field name="name">GRB10</field>
+ <field name="long_name">growth factor receptor-bound protein 10</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p12-p11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRD2">
+ <field name="name">GRD2</field>
+ <field name="long_name">Graves disease, susceptibility to, 2</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.11</field>
+ <field name="info">
+Graves disease, susceptibility to, 2 [MIM:275000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRDX">
+ <field name="name">GRDX</field>
+ <field name="long_name">Graves disease, susceptibility to, X-linked</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11</field>
+ <field name="info">
+Graves disease, susceptibility to, X-linked [MIM:275000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRHL2">
+ <field name="name">GRHL2</field>
+ <field name="long_name">grainyhead-like 2 (Drosophila)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q22</field>
+ <field name="info">
+Deafness, autosomal dominant 28 [MIM:608641]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRHPR">
+ <field name="name">GRHPR</field>
+ <field name="long_name">glyoxylate reductase/hydroxypyruvate reductase</field>
+ <field name="chromosome">9</field>
+ <field name="location">9cen</field>
+ <field name="info">
+Hyperoxaluria, primary, type II [MIM:260000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRIA3">
+ <field name="name">GRIA3</field>
+ <field name="long_name">glutamate receptor, ionotrophic, AMPA 3</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq25-q26</field>
+ <field name="info">
+Mental retardation, X-linked 94 [MIM:300699]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRIK1">
+ <field name="name">GRIK1</field>
+ <field name="long_name">glutamate receptor, ionotropic, kainate 1</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRIK2">
+ <field name="name">GRIK2</field>
+ <field name="long_name">glutamate receptor, ionotropic, kainate 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+Mental retardation, autosomal recessive, 6 [MIM:611092]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRIK3">
+ <field name="name">GRIK3</field>
+ <field name="long_name">glutamate receptor, ionotropic, kainate 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34-p33</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRIK4">
+ <field name="name">GRIK4</field>
+ <field name="long_name">glutamate receptor, ionotropic, kainate 4</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRIN2A">
+ <field name="name">GRIN2A</field>
+ <field name="long_name">glutamate receptor, ionotropic, N-methyl D-aspartate 2A</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRIN2B">
+ <field name="name">GRIN2B</field>
+ <field name="long_name">glutamate receptor, ionotropic, N-methyl D-aspartate 2B</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRK1">
+ <field name="name">GRK1</field>
+ <field name="long_name">G protein-coupled receptor kinase 1</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q34</field>
+ <field name="info">
+Oguchi disease-2 [MIM:258100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRK5">
+ <field name="name">GRK5</field>
+ <field name="long_name">G protein-coupled receptor kinase 5</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24-qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRM3">
+ <field name="name">GRM3</field>
+ <field name="long_name">glutamate receptor, metabotropic 3</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.1-q21.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRM6">
+ <field name="name">GRM6</field>
+ <field name="long_name">glutamate receptor, metabotropic 6</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q35</field>
+ <field name="info">
+Night blindness, congenital stationary, type 1B [MIM:257270]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRM7">
+ <field name="name">GRM7</field>
+ <field name="long_name">glutamate receptor, metabotropic 7</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26.1-p25.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRN">
+ <field name="name">GRN</field>
+ <field name="long_name">granulin</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.32</field>
+ <field name="info">
+Frontotemporal lobar degeneration with ubiquitin-positive inclusions [MIM:607485]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GRPR">
+ <field name="name">GRPR</field>
+ <field name="long_name">gastrin-releasing peptide receptor</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3-p21.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSK3B">
+ <field name="name">GSK3B</field>
+ <field name="long_name">glycogen synthase kinase 3 beta</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSM1">
+ <field name="name">GSM1</field>
+ <field name="long_name">geniospasm 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q13-q21</field>
+ <field name="info">
+Geniospasm</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSN">
+ <field name="name">GSN</field>
+ <field name="long_name">gelsolin (amyloidosis, Finnish type)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+Amyloidosis, Finnish type [MIM:105120]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSPT1">
+ <field name="name">GSPT1</field>
+ <field name="long_name">G1 to S phase transition 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSR">
+ <field name="name">GSR</field>
+ <field name="long_name">glutathione reductase</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21.1</field>
+ <field name="info">
+Hemolytic anemia due to glutathione reductase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSS">
+ <field name="name">GSS</field>
+ <field name="long_name">glutathione synthetase</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11.2</field>
+ <field name="info">
+Hemolytic anemia due to glutathione synthetase deficiency [MIM:231900]
+Glutathione synthetase deficiency [MIM:266130]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSTA1">
+ <field name="name">GSTA1</field>
+ <field name="long_name">glutathione S-transferase alpha 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSTA2">
+ <field name="name">GSTA2</field>
+ <field name="long_name">glutathione S-transferase alpha 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSTA3">
+ <field name="name">GSTA3</field>
+ <field name="long_name">glutathione S-transferase alpha 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSTM1">
+ <field name="name">GSTM1</field>
+ <field name="long_name">glutathione S-transferase mu 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSTM3">
+ <field name="name">GSTM3</field>
+ <field name="long_name">glutathione S-transferase mu 3 (brain)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSTM4">
+ <field name="name">GSTM4</field>
+ <field name="long_name">glutathione S-transferase mu 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSTO1">
+ <field name="name">GSTO1</field>
+ <field name="long_name">glutathione S-transferase omega 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSTP1">
+ <field name="name">GSTP1</field>
+ <field name="long_name">glutathione S-transferase pi 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSTT1">
+ <field name="name">GSTT1</field>
+ <field name="long_name">glutathione S-transferase theta 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSTT2">
+ <field name="name">GSTT2</field>
+ <field name="long_name">glutathione S-transferase theta 2</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GSTZ1">
+ <field name="name">GSTZ1</field>
+ <field name="long_name">glutathione transferase zeta 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3</field>
+ <field name="info">
+Tyrosinemia, type Ib</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GTF2H1">
+ <field name="name">GTF2H1</field>
+ <field name="long_name">general transcription factor IIH, polypeptide 1, 62kDa</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.1-p14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GTF2H5">
+ <field name="name">GTF2H5</field>
+ <field name="long_name">general transcription factor IIH, polypeptide 5</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25.3</field>
+ <field name="info">
+Trichothiodystrophy, complementation group A [MIM:601675]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GTF2IRD1">
+ <field name="name">GTF2IRD1</field>
+ <field name="long_name">GTF2I repeat domain containing 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GTS">
+ <field name="name">GTS</field>
+ <field name="long_name">Gilles de la Tourette syndrome</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Tourette syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GUCA1A">
+ <field name="name">GUCA1A</field>
+ <field name="long_name">guanylate cyclase activator 1A (retina)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.1</field>
+ <field name="info">
+Cone dystrophy-3 [MIM:602093]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GUCA1B">
+ <field name="name">GUCA1B</field>
+ <field name="long_name">guanylate cyclase activator 1B (retina)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="GUCY2D">
+ <field name="name">GUCY2D</field>
+ <field name="long_name">guanylate cyclase 2D, membrane (retina-specific)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.1</field>
+ <field name="info">
+Leber congenital amaurosis 1 [MIM:204000]
+Cone-rod dystrophy 6 [MIM:601777]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GULOP">
+ <field name="name">GULOP</field>
+ <field name="long_name">gulonolactone (L-) oxidase pseudogene</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21.1</field>
+ <field name="info">
+Scurvy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GUSB">
+ <field name="name">GUSB</field>
+ <field name="long_name">glucuronidase, beta</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.11</field>
+ <field name="info">
+Mucopolysaccharidosis VII [MIM:253220]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GUST">
+ <field name="name">GUST</field>
+ <field name="long_name">Gustavson mental retardation syndrome (with microcephaly, optic</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26</field>
+ <field name="info">
+Gustavson syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GYPA">
+ <field name="name">GYPA</field>
+ <field name="long_name">glycophorin A (MNS blood group)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q28.2-q31.1</field>
+ <field name="info">
+Blood group, MN
+Malaria, resistance to [MIM:611162]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GYPB">
+ <field name="name">GYPB</field>
+ <field name="long_name">glycophorin B (MNS blood group)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q28-q31</field>
+ <field name="info">
+Blood group, Ss</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GYPC">
+ <field name="name">GYPC</field>
+ <field name="long_name">glycophorin C (Gerbich blood group)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14-q21</field>
+ <field name="info">
+Malaria, resistance to [MIM:611162]
+Blood group, Gerbich</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GYS1">
+ <field name="name">GYS1</field>
+ <field name="long_name">glycogen synthase 1 (muscle)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+Glycogen storage disease 0, muscle [MIM:611556]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GYS2">
+ <field name="name">GYS2</field>
+ <field name="long_name">glycogen synthase 2 (liver)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p12.2</field>
+ <field name="info">
+Glycogen storage disease, type 0 [MIM:240600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="GZMB">
+ <field name="name">GZMB</field>
+ <field name="long_name">granzyme B (granzyme 2, cytotoxic T-lymphocyte-associated serine esterase 1)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="H19">
+ <field name="name">H19</field>
+ <field name="long_name">H19, imprinted maternally expressed transcript (non-protein coding)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Beckwith-Wiedemann syndrome [MIM:130650]
+Silver-Russell syndrome [MIM:180860]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="H6PD">
+ <field name="name">H6PD</field>
+ <field name="long_name">hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Cortisone reductase deficiency [MIM:604931]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HABP2">
+ <field name="name">HABP2</field>
+ <field name="long_name">hyaluronan binding protein 2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q25-q26</field>
+ <field name="info">
+Carotid stenosis, susceptibility to
+Venous thromboembolism, susceptibility to [MIM:188050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HADHA">
+ <field name="name">HADHA</field>
+ <field name="long_name">hydroxyacyl-Coenzyme A dehydrogenase/3-ketoacyl-Coenzyme A thiolase/enoyl-Coenzyme A hydratase (trifunctional protein), alpha subunit</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p23</field>
+ <field name="info">
+LCHAD deficiency [MIM:609016]
+Trifunctional protein deficiency [MIM:609015]
+HELLP syndrome, maternal, of pregnancy [MIM:609016]
+Fatty liver, acute, of pregnancy [MIM:609016]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HADHB">
+ <field name="name">HADHB</field>
+ <field name="long_name">hydroxyacyl-Coenzyme A dehydrogenase/3-ketoacyl-Coenzyme A thiolase/enoyl-Coenzyme A hydratase (trifunctional protein), beta subunit</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p23</field>
+ <field name="info">
+Trifunctional protein deficiency [MIM:609015]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HAGH">
+ <field name="name">HAGH</field>
+ <field name="long_name">hydroxyacylglutathione hydrolase</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13</field>
+ <field name="info">
+Glyoxalase II deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HAL">
+ <field name="name">HAL</field>
+ <field name="long_name">histidine ammonia-lyase</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q22-q23</field>
+ <field name="info">
+Histidinemia [MIM:235800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HAMP">
+ <field name="name">HAMP</field>
+ <field name="long_name">hepcidin antimicrobial peptide</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+Hemochromatosis, juvenile [MIM:602390]
+Hemochromatosis, juvenile, digenic [MIM:602390]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HARS">
+ <field name="name">HARS</field>
+ <field name="long_name">histidyl-tRNA synthetase</field>
+ <field name="chromosome">5</field>
+ <field name="location">5</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HAVCR1">
+ <field name="name">HAVCR1</field>
+ <field name="long_name">hepatitis A virus cellular receptor 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q33.2</field>
+ <field name="info">
+Atopy, resistance to [MIM:147050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HAX1">
+ <field name="name">HAX1</field>
+ <field name="long_name">HCLS1 associated protein X-1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21.3</field>
+ <field name="info">
+Neutropenia, severe congenital, autosomal recessive 3 [MIM:610738]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HBA1">
+ <field name="name">HBA1</field>
+ <field name="long_name">hemoglobin, alpha 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16pter-p13.3</field>
+ <field name="info">
+Thalassemias, alpha- [MIM:604131]
+Methemoglobinemias, alpha-
+Erythremias, alpha-
+Heinz body anemias, alpha- [MIM:140700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HBA2">
+ <field name="name">HBA2</field>
+ <field name="long_name">hemoglobin, alpha 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16pter-p13.3</field>
+ <field name="info">
+Thalassemia, alpha- [MIM:604131]
+Hemoglobin H disease
+Heinz body anemia [MIM:140700]
+Erythrocytosis
+Hypochromic microcytic anemia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HBBP1">
+ <field name="name">HBBP1</field>
+ <field name="long_name">hemoglobin, beta pseudogene 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Sickle cell anemia [MIM:603903]
+Thalassemias, beta- [MIM:604131]
+Erythremias, beta-
+Methemoglobinemias, beta-
+Heinz body anemias, beta- [MIM:140700]
+Thalassemia-beta, dominant inclusion-body [MIM:603902]
+Hereditary persistence of fetal hemoglobin</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HBB">
+ <field name="name">HBB</field>
+ <field name="long_name">hemoglobin, beta</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Sickle cell anemia [MIM:603903]
+Thalassemias, beta- [MIM:604131]
+Erythremias, beta-
+Methemoglobinemias, beta-
+Heinz body anemias, beta- [MIM:140700]
+Thalassemia-beta, dominant inclusion-body [MIM:603902]
+Hereditary persistence of fetal hemoglobin</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HBD">
+ <field name="name">HBD</field>
+ <field name="long_name">hemoglobin, delta</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Thalassemia, delta-
+Thalassemia due to Hb Lepore</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HBE1">
+ <field name="name">HBE1</field>
+ <field name="long_name">hemoglobin, epsilon 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HBEGF">
+ <field name="name">HBEGF</field>
+ <field name="long_name">heparin-binding EGF-like growth factor</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q23</field>
+ <field name="info">
+Diphtheria, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HBG1">
+ <field name="name">HBG1</field>
+ <field name="long_name">hemoglobin, gamma A</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Fetal hemoglobin quantitative trait locus 1 [MIM:141749]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HBG2">
+ <field name="name">HBG2</field>
+ <field name="long_name">hemoglobin, gamma G</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Fetal hemoglobin quantitative trait locus 1 [MIM:141749]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HBHR">
+ <field name="name">HBHR</field>
+ <field name="long_name">alpha-thalassemia/mental retardation syndrome, type 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16pter-p13.3</field>
+ <field name="info">
+Alpha-thalassemia/mental retardation syndrome, type 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HBN1">
+ <field name="name">HBN1</field>
+ <field name="long_name">Progressive familial heart block, type I, locus 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2-q13.3</field>
+ <field name="info">
+Heart block, progressive familial, type IB [MIM:113900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HBZ">
+ <field name="name">HBZ</field>
+ <field name="long_name">hemoglobin, zeta</field>
+ <field name="chromosome">16</field>
+ <field name="location">16pter-p13.3</field>
+ <field name="info">
+Alpha-Thalassemia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HCA1">
+ <field name="name">HCA1</field>
+ <field name="long_name">Hypercalciuria, absorptive, 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q33-qter</field>
+ <field name="info">
+Hypercalciuria, absorptive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HCCS">
+ <field name="name">HCCS</field>
+ <field name="long_name">holocytochrome c synthase (cytochrome c heme-lyase)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22</field>
+ <field name="info">
+Microphthalmia, syndromic 7 [MIM:309801]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HCK">
+ <field name="name">HCK</field>
+ <field name="long_name">hemopoietic cell kinase</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11-q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HCL3">
+ <field name="name">HCL3</field>
+ <field name="long_name">hair color 3 (brown)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q11.2-q12</field>
+ <field name="info">
+Albinism, oculocutaneous, type II [MIM:203200]
+Albinism, brown oculocutaneous [MIM:203200]
+Skin/hair/eye pigmentation 1, blue/nonblue eyes [MIM:227220]
+Skin/hair/eye pigmentation 1, blond/brown hair [MIM:227220]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HCLS1">
+ <field name="name">HCLS1</field>
+ <field name="long_name">hematopoietic cell-specific Lyn substrate 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HCN2">
+ <field name="name">HCN2</field>
+ <field name="long_name">hyperpolarization activated cyclic nucleotide-gated potassium channel 2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HCN4">
+ <field name="name">HCN4</field>
+ <field name="long_name">hyperpolarization activated cyclic nucleotide-gated potassium channel 4</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q24-q25</field>
+ <field name="info">
+Sick sinus syndrome 2 [MIM:163800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HCRT">
+ <field name="name">HCRT</field>
+ <field name="long_name">hypocretin (orexin) neuropeptide precursor</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+Narcolepsy 1 [MIM:161400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HDAC9">
+ <field name="name">HDAC9</field>
+ <field name="long_name">histone deacetylase 9</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p21-p15</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HDLC3">
+ <field name="name">HDLC3</field>
+ <field name="long_name">High density lipoprotein cholesterol, low serum, 3</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.1</field>
+ <field name="info">
+High density lipoprotein cholesterol, low serum, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HDLCQ1">
+ <field name="name">HDLCQ1</field>
+ <field name="long_name">high density lipoprotein cholesterol level QTL 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p</field>
+ <field name="info">
+High density lipoprotein cholesterol level QTL 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HDLCQ4">
+ <field name="name">HDLCQ4</field>
+ <field name="long_name">High density lipoprotein cholesterol level QTL 4</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q32.3</field>
+ <field name="info">
+High density lipoprotein cholesterol level QTL 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HDLCQ5">
+ <field name="name">HDLCQ5</field>
+ <field name="long_name">High density lipoprotein cholesterol level QTL 5</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q24-q26</field>
+ <field name="info">
+High density lipoprotein cholesterol level QTL 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HDLCQ6">
+ <field name="name">HDLCQ6</field>
+ <field name="long_name">High density lipoprotein cholesterol level QTL 6</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q23-q24</field>
+ <field name="info">
+High density lipoprotein cholesterol level QTL 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HDPA">
+ <field name="name">HDPA</field>
+ <field name="long_name">Hodgkin disease, susceptibility, pseudoautosomal</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xpter-p22.32</field>
+ <field name="info">
+Hodgkin disease susceptibility, pseudoautosomal</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HEMC">
+ <field name="name">HEMC</field>
+ <field name="long_name">hemangioma, capillary, hereditary</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31-q33</field>
+ <field name="info">
+Hemangioma, capillary infantile</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HERC2">
+ <field name="name">HERC2</field>
+ <field name="long_name">hect domain and RLD 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q13.1</field>
+ <field name="info">
+Skin/hair/eye pigmentation 1, blue/nonblue eyes [MIM:227220]
+Skin/hair/eye pigmentation 1, blond/brown hair [MIM:227220]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HES7">
+ <field name="name">HES7</field>
+ <field name="long_name">hairy and enhancer of split 7 (Drosophila)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HESX1">
+ <field name="name">HESX1</field>
+ <field name="long_name">HESX homeobox 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.2-p21.1</field>
+ <field name="info">
+Septooptic dysplasia [MIM:182230]
+Pituitary hormone deficiency, combined, HESX1-related [MIM:182230]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HEXA">
+ <field name="name">HEXA</field>
+ <field name="long_name">hexosaminidase A (alpha polypeptide)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q23-q24</field>
+ <field name="info">
+Tay-Sachs disease [MIM:272800]
+GM2-gangliosidosis, several forms [MIM:272800]
+Hex A pseudodeficiency [MIM:272800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HEXB">
+ <field name="name">HEXB</field>
+ <field name="long_name">hexosaminidase B (beta polypeptide)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13</field>
+ <field name="info">
+Sandhoff disease, infantile, juvenile, and adult forms [MIM:268800]
+Spinal muscular atrophy, juvenile</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HEY">
+ <field name="name">HEY</field>
+ <field name="long_name">unknown</field>
+ <field name="chromosome">Y</field>
+ <field name="location">Yq</field>
+ <field name="info">
+Hairy ears, Y-linked</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HFE2">
+ <field name="name">HFE2</field>
+ <field name="long_name">hemochromatosis type 2 (juvenile)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+Hemochromatosis, juvenile [MIM:602390]
+Hemochromatosis, juvenile, digenic [MIM:602390]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HFE">
+ <field name="name">HFE</field>
+ <field name="long_name">hemochromatosis</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Hemochromatosis
+Transferrin serum level QTL [MIM:190000]
+Microvascular complications of diabetes 7 [MIM:612635]
+Porphyria variegata, susceptibility to [MIM:176200]
+Porphyria cutanea tarda, susceptibility to [MIM:176100]
+Alzheimer disease, susceptibility to [MIM:104300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HFM">
+ <field name="name">HFM</field>
+ <field name="long_name">Hemifacial microsomia</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32</field>
+ <field name="info">
+Hemifacial microsomia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HGD">
+ <field name="name">HGD</field>
+ <field name="long_name">homogentisate 1,2-dioxygenase (homogentisate oxidase)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21-q23</field>
+ <field name="info">
+Alkaptonuria [MIM:203500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HGF">
+ <field name="name">HGF</field>
+ <field name="long_name">hepatocyte growth factor (hepapoietin A; scatter factor)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HGSNAT">
+ <field name="name">HGSNAT</field>
+ <field name="long_name">heparan-alpha-glucosaminide N-acetyltransferase</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p11.1</field>
+ <field name="info">
+Sanfilippo syndrome, type C [MIM:252930]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HHC2">
+ <field name="name">HHC2</field>
+ <field name="long_name">hypocalciuric hypercalcemia 2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Hypocalciuric hypercalcemia, type II</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HHC3">
+ <field name="name">HHC3</field>
+ <field name="long_name">hypocalciuric hypercalcemia 3 (Oklahoma type)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+Hypercalciuric hypercalcemia, type III</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HHEX">
+ <field name="name">HHEX</field>
+ <field name="long_name">hematopoietically expressed homeobox</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HHT4">
+ <field name="name">HHT4</field>
+ <field name="long_name">Telangiectasia, hereditary hemorrhagic, type 4</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14</field>
+ <field name="info">
+Telangiectasia, hereditary hemorrhagic, type 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HIBCH">
+ <field name="name">HIBCH</field>
+ <field name="long_name">3-hydroxyisobutyryl-Coenzyme A hydrolase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q32.2</field>
+ <field name="info">
+3-hydroxyisobutryl-CoA hydrolase deficiency [MIM:250620]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HIF1AN">
+ <field name="name">HIF1AN</field>
+ <field name="long_name">hypoxia inducible factor 1, alpha subunit inhibitor</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HIF1A">
+ <field name="name">HIF1A</field>
+ <field name="long_name">hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q21-q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HIP1">
+ <field name="name">HIP1</field>
+ <field name="long_name">huntingtin interacting protein 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.23</field>
+ <field name="info">
+Prostate cancer, progression of [MIM:176807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HJCD">
+ <field name="name">HJCD</field>
+ <field name="long_name">Histiocytosis with joint contractures and sensorineural deafness</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q25</field>
+ <field name="info">
+Faisalabad histiocytosis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HK1">
+ <field name="name">HK1</field>
+ <field name="long_name">hexokinase 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22</field>
+ <field name="info">
+Hemolytic anemia due to hexokinase deficiency [MIM:235700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HK2">
+ <field name="name">HK2</field>
+ <field name="long_name">hexokinase 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLA-A">
+ <field name="name">HLA-A</field>
+ <field name="long_name">major histocompatibility complex, class I, A</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Ankylosing spondylitis, susceptibility to, 1 [MIM:106300]
+Stevens-Johnson syndrome, susceptibility to [MIM:608579]
+Abacavir hypersensitivity, susceptibility to (3) 17</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLA-B">
+ <field name="name">HLA-B</field>
+ <field name="long_name">major histocompatibility complex, class I, B</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Spondyloarthropathy, susceptibility to, 1 [MIM:106300]
+Stevens-Johnson syndrome, carbamazepine-induced, susceptibility to [MIM:608579]
+Abacavir hypersensitivity, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLA-C">
+ <field name="name">HLA-C</field>
+ <field name="long_name">major histocompatibility complex, class I, C</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Psoriasis, early onset, susceptibility to [MIM:177900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLA-DMB">
+ <field name="name">HLA-DMB</field>
+ <field name="long_name">major histocompatibility complex, class II, DM beta</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLA-DPB1">
+ <field name="name">HLA-DPB1</field>
+ <field name="long_name">major histocompatibility complex, class II, DP beta 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Beryllium disease, chronic, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLA-DPB2">
+ <field name="name">HLA-DPB2</field>
+ <field name="long_name">major histocompatibility complex, class II, DP beta 2 (pseudogene)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Stickler syndrome, type III [MIM:184840]
+Otospondylomegaepiphyseal dysplasia [MIM:215150]
+Weissenbacher-Zweymuller syndrome [MIM:277610]
+Deafness, autosomal dominant 13 [MIM:601868]
+Deafness, autosomal recessive 53 [MIM:609706]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLA-DQA1">
+ <field name="name">HLA-DQA1</field>
+ <field name="long_name">major histocompatibility complex, class II, DQ alpha 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Celiac disease, susceptibility to [MIM:212750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLA-DQB1">
+ <field name="name">HLA-DQB1</field>
+ <field name="long_name">major histocompatibility complex, class II, DQ beta 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Creutzfeldt-Jakob disease, variant, resistance to [MIM:123400]
+Multiple sclerosis, susceptibility to [MIM:126200]
+Celiac disease, susceptibility to [MIM:212750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLA-DRA">
+ <field name="name">HLA-DRA</field>
+ <field name="long_name">major histocompatibility complex, class II, DR alpha</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLA-DRB5">
+ <field name="name">HLA-DRB5</field>
+ <field name="long_name">major histocompatibility complex, class II, DR beta 5</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLA-E">
+ <field name="name">HLA-E</field>
+ <field name="long_name">major histocompatibility complex, class I, E</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLA-G">
+ <field name="name">HLA-G</field>
+ <field name="long_name">major histocompatibility complex, class I, G</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Asthma, susceptibility to [MIM:600807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLA-H">
+ <field name="name">HLA-H</field>
+ <field name="long_name">major histocompatibility complex, class I, H (pseudogene)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Hemochromatosis
+Transferrin serum level QTL [MIM:190000]
+Microvascular complications of diabetes 7 [MIM:612635]
+Porphyria variegata, susceptibility to [MIM:176200]
+Porphyria cutanea tarda, susceptibility to [MIM:176100]
+Alzheimer disease, susceptibility to [MIM:104300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLCS">
+ <field name="name">HLCS</field>
+ <field name="long_name">holocarboxylase synthetase (biotin-(proprionyl-Coenzyme A-carboxylase (ATP-hydrolysing)) ligase)</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.1</field>
+ <field name="info">
+Holocarboxylase synthetase deficiency [MIM:253270]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLF">
+ <field name="name">HLF</field>
+ <field name="long_name">hepatic leukemia factor</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q22</field>
+ <field name="info">
+acute lymphoblastic leukemia,preB-cell,with t(17;19)(q22;p13) translocation (see TCF3),associated with CDNK2A and/or CDKN2B deletion</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HLN2">
+ <field name="name">HLN2</field>
+ <field name="long_name">Huntington-like neurodegenerative disorder 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15.3</field>
+ <field name="info">
+Huntington disease-like 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMBS">
+ <field name="name">HMBS</field>
+ <field name="long_name">hydroxymethylbilane synthase</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.3</field>
+ <field name="info">
+Porphyria, acute intermittent [MIM:176000]
+Porphyria, acute intermittent, nonerythroid variant [MIM:176000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMCN1">
+ <field name="name">HMCN1</field>
+ <field name="long_name">hemicentin 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q24-q25</field>
+ <field name="info">
+Macular degeneration, age-related, 1 [MIM:603075]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMGA1">
+ <field name="name">HMGA1</field>
+ <field name="long_name">high mobility group AT-hook 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21</field>
+ <field name="info">
+Lipoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMGA2">
+ <field name="name">HMGA2</field>
+ <field name="long_name">high mobility group AT-hook 2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q14.3</field>
+ <field name="info">
+Lipoma
+Salivary adenoma
+Uterine leiomyoma
+Lipomatosis, multiple [MIM:151900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMGCL">
+ <field name="name">HMGCL</field>
+ <field name="long_name">3-hydroxymethyl-3-methylglutaryl-Coenzyme A lyase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1pter-p33</field>
+ <field name="info">
+HMG-CoA lyase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMGCR">
+ <field name="name">HMGCR</field>
+ <field name="long_name">3-hydroxy-3-methylglutaryl-Coenzyme A reductase</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13.3-q14</field>
+ <field name="info">
+Statins, attenuated cholesterol lowering by
+Low density lipoprotein cholesterol level QTL 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMGCS2">
+ <field name="name">HMGCS2</field>
+ <field name="long_name">3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 (mitochondrial)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13-p12</field>
+ <field name="info">
+HMG-CoA synthase-2 deficiency [MIM:605911]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMHA1">
+ <field name="name">HMHA1</field>
+ <field name="long_name">histocompatibility (minor) HA-1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMMR">
+ <field name="name">HMMR</field>
+ <field name="long_name">hyaluronan-mediated motility receptor (RHAMM)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q33.2</field>
+ <field name="info">
+Breast cancer, susceptibility to [MIM:114480]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMN7A">
+ <field name="name">HMN7A</field>
+ <field name="long_name">Motor neuronopathy, distal hereditary, type VIIA</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14</field>
+ <field name="info">
+Motor neuronopathy, distal hereditary, with vocal cord paralysis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMNJ">
+ <field name="name">HMNJ</field>
+ <field name="long_name">Distal hereditary motor neuropathy, Jerash type</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21.1-p12</field>
+ <field name="info">
+Neuropathy, distal hereditary motor, Jerash type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMOX1">
+ <field name="name">HMOX1</field>
+ <field name="long_name">heme oxygenase (decycling) 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12</field>
+ <field name="info">
+Heme oxygenase-1 deficiency
+Pulmonary disease, chronic obstructive, susceptibility to [MIM:606963]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMSD">
+ <field name="name">HMSD</field>
+ <field name="long_name">histocompatibility (minor) serpin domain containing</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMSNO">
+ <field name="name">HMSNO</field>
+ <field name="long_name">Neuropathy, hereditary motor and sensory, Okinawa type</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q13.1</field>
+ <field name="info">
+Neuropathy, hereditary motor and sensory, Okinawa type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HMX1">
+ <field name="name">HMX1</field>
+ <field name="long_name">H6 family homeobox 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.1</field>
+ <field name="info">
+Oculoauricular syndrome [MIM:612109]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HNF1A">
+ <field name="name">HNF1A</field>
+ <field name="long_name">HNF1 homeobox A</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.2</field>
+ <field name="info">
+MODY, type III [MIM:600496]
+Diabetes mellitus, noninsulin-dependent, 2 [MIM:125853]
+Diabetes mellitus, insulin-dependent [MIM:222100]
+Hepatic adenoma [MIM:142330]
+Renal cell carcinoma [MIM:144700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HNF1B">
+ <field name="name">HNF1B</field>
+ <field name="long_name">HNF1 homeobox B</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12</field>
+ <field name="info">
+Renal cysts and diabetes syndrome [MIM:137920]
+Diabetes mellitus, noninsulin-dependent [MIM:125853]
+Renal cell carcinoma [MIM:144700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HNF4A">
+ <field name="name">HNF4A</field>
+ <field name="long_name">hepatocyte nuclear factor 4, alpha</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q12-q13.1</field>
+ <field name="info">
+MODY, type I [MIM:125850]
+Diabetes mellitus, noninsulin-dependent [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HNMT">
+ <field name="name">HNMT</field>
+ <field name="long_name">histamine N-methyltransferase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q22</field>
+ <field name="info">
+Asthma, susceptibility to [MIM:600807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HNP1">
+ <field name="name">HNP1</field>
+ <field name="long_name">Hypertensive nephropathy</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q31-q32</field>
+ <field name="info">
+Hypertensive nephropathy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HOXA10">
+ <field name="name">HOXA10</field>
+ <field name="long_name">homeobox A10</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15-p14.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HOXA11">
+ <field name="name">HOXA11</field>
+ <field name="long_name">homeobox A11</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15-p14.2</field>
+ <field name="info">
+Radioulnar synostosis with amegakaryocytic thrombocytopenia [MIM:605432]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HOXA13">
+ <field name="name">HOXA13</field>
+ <field name="long_name">homeobox A13</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15-p14.2</field>
+ <field name="info">
+Hand-foot-uterus syndrome [MIM:140000]
+Guttmacher syndrome [MIM:176305]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HOXA1">
+ <field name="name">HOXA1</field>
+ <field name="long_name">homeobox A1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15.3</field>
+ <field name="info">
+Bosley-Salih-Alorainy syndrome [MIM:601536]
+Athabaskan brainstem dysgenesis syndrome [MIM:601536]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HOXA2">
+ <field name="name">HOXA2</field>
+ <field name="long_name">homeobox A2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15-p14</field>
+ <field name="info">
+Microtia, hearing impairment, and cleft palate [MIM:612290]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HOXA4">
+ <field name="name">HOXA4</field>
+ <field name="long_name">homeobox A4</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15-p14.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HOXB6">
+ <field name="name">HOXB6</field>
+ <field name="long_name">homeobox B6</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HOXD10">
+ <field name="name">HOXD10</field>
+ <field name="long_name">homeobox D10</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31-q32</field>
+ <field name="info">
+Vertical talus, congenital [MIM:192950]
+Charcot-Marie-Tooth disease, foot deformity of</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HOXD13">
+ <field name="name">HOXD13</field>
+ <field name="long_name">homeobox D13</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31-q32</field>
+ <field name="info">
+Synpolydactyly, type II [MIM:186000]
+Brachydactyly, type E [MIM:113300]
+Brachydactyly, type D [MIM:113200]
+Synpolydactyly with foot anomalies [MIM:186000]
+Syndactyly, type V [MIM:186300]
+Brachydactyly-syndactyly syndrome [MIM:610713]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HOXD4">
+ <field name="name">HOXD4</field>
+ <field name="long_name">homeobox D4</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31-q32</field>
+ <field name="info">
+Leukemia, acute lymphoblastic, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPC10">
+ <field name="name">HPC10</field>
+ <field name="long_name">Prostate cancer, hereditary, 10</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24</field>
+ <field name="info">
+Prostate cancer, hereditary, 10</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPC14">
+ <field name="name">HPC14</field>
+ <field name="long_name">Prostate cancer, hereditary, 14</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Prostate cancer, hereditary, 14</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPC15">
+ <field name="name">HPC15</field>
+ <field name="long_name">Prostate cancer, hereditary, 15</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+Prostate cancer, hereditary, 15</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPC1">
+ <field name="name">HPC1</field>
+ <field name="long_name">hereditary prostate cancer 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q25</field>
+ <field name="info">
+Prostate cancer 1, 176807 [MIM:601518]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPC3">
+ <field name="name">HPC3</field>
+ <field name="long_name">Prostate cancer, hereditary, 3</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13</field>
+ <field name="info">
+Prostate cancer, susceptibility to, 3 [MIM:176807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPC4">
+ <field name="name">HPC4</field>
+ <field name="long_name">Prostate cancer, hereditary, 4</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p11-q21</field>
+ <field name="info">
+Prostate cancer, susceptibility to, 4 [MIM:176807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPC5">
+ <field name="name">HPC5</field>
+ <field name="long_name">prostate cancer, hereditary, 5</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26</field>
+ <field name="info">
+Prostate cancer, hereditary, 5 [MIM:176807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPC6">
+ <field name="name">HPC6</field>
+ <field name="long_name">Prostate cancer, susceptibility to</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.3</field>
+ <field name="info">
+Prostate cancer, susceptibility to [MIM:176807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPC7">
+ <field name="name">HPC7</field>
+ <field name="long_name">Prostate cancer, hereditary, 7</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q12</field>
+ <field name="info">
+Prostate cancer, hereditary, 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPC9">
+ <field name="name">HPC9</field>
+ <field name="long_name">Prostate cancer, hereditary, 9</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+Prostate cancer, hereditary, 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPCQTL19">
+ <field name="name">HPCQTL19</field>
+ <field name="long_name">Prostate cancer aggressiveness quantitative trait locus on chromosome 19</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q</field>
+ <field name="info">
+Prostate cancer aggressiveness QTL [MIM:176807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPCX2">
+ <field name="name">HPCX2</field>
+ <field name="long_name">Prostate cancer, hereditary, X-linked 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.22</field>
+ <field name="info">
+Prostate cancer, hereditary, X-linked 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPD">
+ <field name="name">HPD</field>
+ <field name="long_name">4-hydroxyphenylpyruvate dioxygenase</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24-qter</field>
+ <field name="info">
+Tyrosinemia, type III [MIM:276710]
+Hawkinsinuria [MIM:140350]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPE1">
+ <field name="name">HPE1</field>
+ <field name="long_name">holoprosencephaly 1, alobar</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Holoprosencephaly-1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPE6">
+ <field name="name">HPE6</field>
+ <field name="long_name">holoprosencephaly 6</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.1-q37.3</field>
+ <field name="info">
+Holoprosencephaly-6 [MIM:236100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPE8">
+ <field name="name">HPE8</field>
+ <field name="long_name">holoprosencephaly 8</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q13</field>
+ <field name="info">
+Holoprosencephaly-8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPFH2">
+ <field name="name">HPFH2</field>
+ <field name="long_name">hereditary persistence of fetal hemoglobin, heterocellular, Indian type</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q36</field>
+ <field name="info">
+Hereditary persistence of fetal hemoglobin, heterocellular, Indian type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPGD">
+ <field name="name">HPGD</field>
+ <field name="long_name">hydroxyprostaglandin dehydrogenase 15-(NAD)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q34-q35</field>
+ <field name="info">
+Cranioosteoarthropathy [MIM:259100]
+Hypertrophic osteoarthropathy, primary, autosomal recessive [MIM:259100]
+Digital clubbing, isolated congenital [MIM:119900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPLH1">
+ <field name="name">HPLH1</field>
+ <field name="long_name">hemophagocytic lymphohistiocytosis 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q21.3-q22</field>
+ <field name="info">
+Hemophagocytic lymphohistiocytosis, familial, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPRHP">
+ <field name="name">HPRHP</field>
+ <field name="long_name">Hypophosphatemic rickets and hyperparathyroidism</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q13.1</field>
+ <field name="info">
+Hypophosphatemic rickets and hyperparathyroidism</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPRT1">
+ <field name="name">HPRT1</field>
+ <field name="long_name">hypoxanthine phosphoribosyltransferase 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26-q27.2</field>
+ <field name="info">
+Lesch-Nyhan syndrome [MIM:300322]
+HPRT-related gout [MIM:300323]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPS1">
+ <field name="name">HPS1</field>
+ <field name="long_name">Hermansky-Pudlak syndrome 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23.1</field>
+ <field name="info">
+Hermansky-Pudlak syndrome 1 [MIM:203300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPS3">
+ <field name="name">HPS3</field>
+ <field name="long_name">Hermansky-Pudlak syndrome 3</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q24</field>
+ <field name="info">
+Hermansky-Pudlak syndrome 3 [MIM:203300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPS4">
+ <field name="name">HPS4</field>
+ <field name="long_name">Hermansky-Pudlak syndrome 4</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2-q12.2</field>
+ <field name="info">
+Hermansky-Pudlak syndrome 4 [MIM:203300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPS5">
+ <field name="name">HPS5</field>
+ <field name="long_name">Hermansky-Pudlak syndrome 5</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15-p13</field>
+ <field name="info">
+Hermansky-pudlak syndrome 5 [MIM:203300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPS6">
+ <field name="name">HPS6</field>
+ <field name="long_name">Hermansky-Pudlak syndrome 6</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24.32</field>
+ <field name="info">
+Hermansky-Pudlak syndrome 6 [MIM:203300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPSE">
+ <field name="name">HPSE</field>
+ <field name="long_name">heparanase</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HPT">
+ <field name="name">HPT</field>
+ <field name="long_name">hypoparathyroidism</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26-q27</field>
+ <field name="info">
+Hypoparathyroidism, X-linked</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HP">
+ <field name="name">HP</field>
+ <field name="long_name">haptoglobin</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22.1</field>
+ <field name="info">
+Anhaptoglobinemia
+Hypohaptoglobinemia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HRAS">
+ <field name="name">HRAS</field>
+ <field name="long_name">v-Ha-ras Harvey rat sarcoma viral oncogene homolog</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Bladder cancer, somatic [MIM:109800]
+Costello syndrome [MIM:218040]
+Thyroid carcinoma, follicular, somatic [MIM:188470]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HRD">
+ <field name="name">HRD</field>
+ <field name="long_name">hypoparathyroidism, growth and mental retardation, and dysmorphism</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42-q43</field>
+ <field name="info">
+Kenny-Caffey syndrome-1 [MIM:244460]
+Hypoparathyroidism-retardation-dysmorphism syndrome [MIM:241410]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HRG">
+ <field name="name">HRG</field>
+ <field name="long_name">histidine-rich glycoprotein</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27</field>
+ <field name="info">
+Thrombophilia due to HRG deficiency
+Thrombophilia due to elevated HRG</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HRH2">
+ <field name="name">HRH2</field>
+ <field name="long_name">histamine receptor H2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HRPT3">
+ <field name="name">HRPT3</field>
+ <field name="long_name">Hyperparathyroidism 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p14-p13.3</field>
+ <field name="info">
+Hyperparathyroidism 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HR">
+ <field name="name">HR</field>
+ <field name="long_name">hairless homolog (mouse)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21.2</field>
+ <field name="info">
+Alopecia universalis [MIM:203655]
+Atrichia with papular lesions [MIM:209500]
+Hypotrichosis, Marie Unna type [MIM:146550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HS1BP3">
+ <field name="name">HS1BP3</field>
+ <field name="long_name">HCLS1 binding protein 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p24.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSCR9">
+ <field name="name">HSCR9</field>
+ <field name="long_name">Hirschsprung disease, susceptibility to, 9</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q31.3-q32.3</field>
+ <field name="info">
+Hirschsprung disease, susceptibility to, 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSCRS2">
+ <field name="name">HSCRS2</field>
+ <field name="long_name">Hirschsprung disease, short-segment, 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21</field>
+ <field name="info">
+Hirschsprung disease, short-segment, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSCRS3">
+ <field name="name">HSCRS3</field>
+ <field name="long_name">Hirschsprung disease, short-segment, 3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q12</field>
+ <field name="info">
+Hirschsprung disease, short-segment, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSD11B1">
+ <field name="name">HSD11B1</field>
+ <field name="long_name">hydroxysteroid (11-beta) dehydrogenase 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32-q41</field>
+ <field name="info">
+Cortisone reductase deficiency [MIM:604931]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSD11B2">
+ <field name="name">HSD11B2</field>
+ <field name="long_name">hydroxysteroid (11-beta) dehydrogenase 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22</field>
+ <field name="info">
+Apparent mineralocorticoid excess, hypertension due to
+Hypertension, mild low-renin</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSD17B10">
+ <field name="name">HSD17B10</field>
+ <field name="long_name">hydroxysteroid (17-beta) dehydrogenase 10</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.2</field>
+ <field name="info">
+2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency [MIM:300438]
+Mental retardation, X-linked syndromic 10 [MIM:300220]
+Mental retardation, X-linked 17/31, microduplication [MIM:300705]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSD17B1">
+ <field name="name">HSD17B1</field>
+ <field name="long_name">hydroxysteroid (17-beta) dehydrogenase 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12-q21</field>
+ <field name="info">
+hirsutism with amenorrhea and polycystic ovarian disease</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSD17B2">
+ <field name="name">HSD17B2</field>
+ <field name="long_name">hydroxysteroid (17-beta) dehydrogenase 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.1-q24.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSD17B3">
+ <field name="name">HSD17B3</field>
+ <field name="long_name">hydroxysteroid (17-beta) dehydrogenase 3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22</field>
+ <field name="info">
+Pseudohermaphroditism, male, with gynecomastia [MIM:264300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSD17B4">
+ <field name="name">HSD17B4</field>
+ <field name="long_name">hydroxysteroid (17-beta) dehydrogenase 4</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q2</field>
+ <field name="info">
+D-bifunctional protein deficiency [MIM:261515]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSD3B1">
+ <field name="name">HSD3B1</field>
+ <field name="long_name">hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSD3B2">
+ <field name="name">HSD3B2</field>
+ <field name="long_name">hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13.1</field>
+ <field name="info">
+3-beta-hydroxysteroid dehydrogenase, type II, deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSD3B7">
+ <field name="name">HSD3B7</field>
+ <field name="long_name">hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12-p11.2</field>
+ <field name="info">
+Cholestasis, progressive familial intrahepatic 4 [MIM:607765]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSF4">
+ <field name="name">HSF4</field>
+ <field name="long_name">heat shock transcription factor 4</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q21-q22.1</field>
+ <field name="info">
+Cataract, Marner type [MIM:116800]
+Cataract, lamellar [MIM:116800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSN1B">
+ <field name="name">HSN1B</field>
+ <field name="long_name">Hereditary sensory neuropathy, type IB</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p24-p22</field>
+ <field name="info">
+HSN I with cough and gastroesophageal reflux</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSN2">
+ <field name="name">HSN2</field>
+ <field name="long_name">hereditary sensory neuropathy, type II</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+Pseudohypoaldosteronism, type IIC [MIM:145260]
+Neuropathy, hereditary sensory and autonomic, type II [MIM:201300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSP90AA1">
+ <field name="name">HSP90AA1</field>
+ <field name="long_name">heat shock protein 90kDa alpha (cytosolic), class A member 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSP90B1">
+ <field name="name">HSP90B1</field>
+ <field name="long_name">heat shock protein 90kDa beta (Grp94), member 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q23.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSPA1A">
+ <field name="name">HSPA1A</field>
+ <field name="long_name">heat shock 70kDa protein 1A</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSPA1B">
+ <field name="name">HSPA1B</field>
+ <field name="long_name">heat shock 70kDa protein 1B</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSPA5">
+ <field name="name">HSPA5</field>
+ <field name="long_name">heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSPB1">
+ <field name="name">HSPB1</field>
+ <field name="long_name">heat shock 27kDa protein 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.23</field>
+ <field name="info">
+Neuropathy, distal hereditary motor, type IIB [MIM:608634]
+Charcot-Marie-Tooth disease, axonal, type 2F [MIM:606595]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSPB6">
+ <field name="name">HSPB6</field>
+ <field name="long_name">heat shock protein, alpha-crystallin-related, B6</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSPB8">
+ <field name="name">HSPB8</field>
+ <field name="long_name">heat shock 22kDa protein 8</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24</field>
+ <field name="info">
+Neuropathy, distal hereditary motor, type IIA [MIM:158590]
+Charcot-Marie-Tooth disease, axonal, type 2L [MIM:608673]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSPD1">
+ <field name="name">HSPD1</field>
+ <field name="long_name">heat shock 60kDa protein 1 (chaperonin)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33.1</field>
+ <field name="info">
+Spastic paraplegia-13 [MIM:605280]
+Leukodystrophy, hypomyelinating, 4 [MIM:612233]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSPG2">
+ <field name="name">HSPG2</field>
+ <field name="long_name">heparan sulfate proteoglycan 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.1</field>
+ <field name="info">
+Schwartz-Jampel syndrome, type 1 [MIM:255800]
+Dyssegmental dysplasia, Silverman-Handmaker type [MIM:224410]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HSR">
+ <field name="name">HSR</field>
+ <field name="long_name">Hand skill, relative</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p12-q22</field>
+ <field name="info">
+Handedness</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTC2">
+ <field name="name">HTC2</field>
+ <field name="long_name">hypertrichosis 2 (generalized, congenital)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24-q27.1</field>
+ <field name="info">
+Hypertrichosis, congenital generalized</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTGS">
+ <field name="name">HTGS</field>
+ <field name="long_name">Hypertriglyceridemia, familial</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q11.2-q13.1</field>
+ <field name="info">
+Hypertriglyceridemia, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTN3">
+ <field name="name">HTN3</field>
+ <field name="long_name">histatin 3</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTNB">
+ <field name="name">HTNB</field>
+ <field name="long_name">hypertension with brachydactyly</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p12.2-p11.2</field>
+ <field name="info">
+Hypertension with brachydactyly</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTR1A">
+ <field name="name">HTR1A</field>
+ <field name="long_name">5-hydroxytryptamine (serotonin) receptor 1A</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q11.2-q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTR1B">
+ <field name="name">HTR1B</field>
+ <field name="long_name">5-hydroxytryptamine (serotonin) receptor 1B</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTR2A">
+ <field name="name">HTR2A</field>
+ <field name="long_name">5-hydroxytryptamine (serotonin) receptor 2A</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14-q21</field>
+ <field name="info">
+Schizophrenia, susceptibility to [MIM:181500]
+Obsessive-compulsive disorder, susceptibility to [MIM:164230]
+Seasonal affective disorder, susceptibility to [MIM:608516]
+Alcohol dependence, susceptibility to [MIM:103780]
+Anorexia nervosa, susceptibility to [MIM:606788]
+Major depressive disorder, response to citalopram therapy in [MIM:608516]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTR2B">
+ <field name="name">HTR2B</field>
+ <field name="long_name">5-hydroxytryptamine (serotonin) receptor 2B</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q36.3-q37.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTR2C">
+ <field name="name">HTR2C</field>
+ <field name="long_name">5-hydroxytryptamine (serotonin) receptor 2C</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTR3B">
+ <field name="name">HTR3B</field>
+ <field name="long_name">5-hydroxytryptamine (serotonin) receptor 3B</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTR3E">
+ <field name="name">HTR3E</field>
+ <field name="long_name">5-hydroxytryptamine (serotonin) receptor 3, family member E</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTR5A">
+ <field name="name">HTR5A</field>
+ <field name="long_name">5-hydroxytryptamine (serotonin) receptor 5A</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q36.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTR6">
+ <field name="name">HTR6</field>
+ <field name="long_name">5-hydroxytryptamine (serotonin) receptor 6</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36-p35</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTR7">
+ <field name="name">HTR7</field>
+ <field name="long_name">5-hydroxytryptamine (serotonin) receptor 7 (adenylate cyclase-coupled)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21-q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTRA1">
+ <field name="name">HTRA1</field>
+ <field name="long_name">HtrA serine peptidase 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q25.3-q26.2</field>
+ <field name="info">
+Macular degeneration, age-related, 7 [MIM:610149]
+Macular degeneration, age-related, neovascular type [MIM:610149]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTRA2">
+ <field name="name">HTRA2</field>
+ <field name="long_name">HtrA serine peptidase 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p12</field>
+ <field name="info">
+Parkinson disease 13 [MIM:610297]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTS">
+ <field name="name">HTS</field>
+ <field name="long_name">Hypoptrichosis simplex</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.32-p11.23</field>
+ <field name="info">
+Hypotrichosis simplex</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTT">
+ <field name="name">HTT</field>
+ <field name="long_name">huntingtin</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.1-q12</field>
+ <field name="info">
+Anxiety-related personality traits [MIM:607834]
+Obsessive-compulsive disorder 1 [MIM:164230]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTX2">
+ <field name="name">HTX2</field>
+ <field name="long_name">heterotaxy 2 (autosomal dominant)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q21.1</field>
+ <field name="info">
+Heterotaxy, visceral, 2, autosomal [MIM:605376]
+Double-outlet right ventricle [MIM:217095]
+Transposition of the great arteries, dextro-looped 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HTX3">
+ <field name="name">HTX3</field>
+ <field name="long_name">Heterotaxy, visceral, 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+Heterotaxy, visceral</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HT">
+ <field name="name">HT</field>
+ <field name="long_name">Hashimoto thyroiditis</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q23-q24</field>
+ <field name="info">
+Hashimoto thyroiditis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HUNK">
+ <field name="name">HUNK</field>
+ <field name="long_name">hormonally up-regulated Neu-associated kinase</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HUS1B">
+ <field name="name">HUS1B</field>
+ <field name="long_name">HUS1 checkpoint homolog b (S. pombe)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p25.3-p25.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HUWE1">
+ <field name="name">HUWE1</field>
+ <field name="long_name">HECT, UBA and WWE domain containing 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.2</field>
+ <field name="info">
+Mental retardation, X-linked syndromic, Turner type [MIM:300706]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYAL1">
+ <field name="name">HYAL1</field>
+ <field name="long_name">hyaluronoglucosaminidase 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.3-p21.2</field>
+ <field name="info">
+Mucopolysaccharidosis type IX [MIM:601492]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYALP">
+ <field name="name">HYALP</field>
+ <field name="long_name">Hypoalphalipoproteinemia, primary</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.3</field>
+ <field name="info">
+Hypoalphalipoproteinemia, primary</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYD2">
+ <field name="name">HYD2</field>
+ <field name="long_name">hypodontia, autosomal recessive (2)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q12.1</field>
+ <field name="info">
+Tooth agenesis, selective, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYDIN2">
+ <field name="name">HYDIN2</field>
+ <field name="long_name">hydrocephalus inducing homolog 2 (mouse)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYLS1">
+ <field name="name">HYLS1</field>
+ <field name="long_name">hydrolethalus syndrome 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q24.2</field>
+ <field name="info">
+Hydrolethalus syndrome [MIM:236680]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYMAI">
+ <field name="name">HYMAI</field>
+ <field name="long_name">hydatidiform mole associated and imprinted (non-protein coding)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q24</field>
+ <field name="info">
+Diabetes Mellitus</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYPLIP2">
+ <field name="name">HYPLIP2</field>
+ <field name="long_name">hyperlipidemia, combined, 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p</field>
+ <field name="info">
+Hyperlipidemia, combined, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYT1">
+ <field name="name">HYT1</field>
+ <field name="long_name">Hypertension, essential, susceptibility to, 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q</field>
+ <field name="info">
+Hypertension, essential, susceptibility to, 1 [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYT2">
+ <field name="name">HYT2</field>
+ <field name="long_name">Hypertension, essential, susceptibility to, 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q</field>
+ <field name="info">
+Hypertension, essential, susceptibility to, 2 [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYT3">
+ <field name="name">HYT3</field>
+ <field name="long_name">Hypertension, essential, susceptibility to, 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p25-p24</field>
+ <field name="info">
+Hypertension, essential, susceptibility to, 3 [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYT4">
+ <field name="name">HYT4</field>
+ <field name="long_name">Hypertension, essential, susceptibility to, 4</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p12.2-p12.1</field>
+ <field name="info">
+Hypertension, essential, susceptibility to, 4 [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYT5">
+ <field name="name">HYT5</field>
+ <field name="long_name">Hypertension, essential, susceptibility to, 5</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11-q13</field>
+ <field name="info">
+Hypertension, essential, susceptibility to, 5 [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYT6">
+ <field name="name">HYT6</field>
+ <field name="long_name">Hypertension, essential, susceptibility to, 6</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13-q12</field>
+ <field name="info">
+Hypertension, essential, susceptibility to, 6 [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYT7">
+ <field name="name">HYT7</field>
+ <field name="long_name">Hypertension, essential, susceptibility to, 7</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p14.1-q12.3</field>
+ <field name="info">
+Hypertension, essential, susceptibility to, 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="HYT8">
+ <field name="name">HYT8</field>
+ <field name="long_name">hypertension, essential, susceptibility to, 8</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.2</field>
+ <field name="info">
+Hypertension, essential, susceptibility to, 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IAPP">
+ <field name="name">IAPP</field>
+ <field name="long_name">islet amyloid polypeptide</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p12.3-p12.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD12">
+ <field name="name">IBD12</field>
+ <field name="long_name">Inflammatory bowel disease 12</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.3</field>
+ <field name="info">
+Inflammatory bowel disease 12</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD15">
+ <field name="name">IBD15</field>
+ <field name="long_name">Inflammatory bowel disease-15</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21</field>
+ <field name="info">
+Inflammatory bowel disease-15</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD16">
+ <field name="name">IBD16</field>
+ <field name="long_name">Inflammatory bowel disease-16</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q32</field>
+ <field name="info">
+Inflammatory bowel disease-16</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD18">
+ <field name="name">IBD18</field>
+ <field name="long_name">Inflammatory bowel disease-18</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13.1</field>
+ <field name="info">
+Inflammatory bowel disease-18</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD19">
+ <field name="name">IBD19</field>
+ <field name="long_name">Inflammatory bowel disease 19</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q33.1</field>
+ <field name="info">
+Inflammatory bowel disease 19</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD20">
+ <field name="name">IBD20</field>
+ <field name="long_name">Inflammatory bowel disease-20</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23-q24</field>
+ <field name="info">
+Inflammatory bowel disease-20</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD21">
+ <field name="name">IBD21</field>
+ <field name="long_name">Inflammatory bowel disease-21</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11</field>
+ <field name="info">
+Inflammatory bowel disease-21</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD22">
+ <field name="name">IBD22</field>
+ <field name="long_name">Inflammatory bowel disease-22</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.2</field>
+ <field name="info">
+Inflammatory bowel disease-22</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD23">
+ <field name="name">IBD23</field>
+ <field name="long_name">Inflammatory bowel disease-23</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32.1</field>
+ <field name="info">
+Inflammatory bowel disease-23</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD24">
+ <field name="name">IBD24</field>
+ <field name="long_name">Inflammatory bowel disease-24</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13</field>
+ <field name="info">
+Inflammatory bowel disease-24</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD25">
+ <field name="name">IBD25</field>
+ <field name="long_name">Inflammatory bowel disease-25</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22</field>
+ <field name="info">
+Inflammatory bowel disease-25</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD26">
+ <field name="name">IBD26</field>
+ <field name="long_name">Inflammatory bowel disease-26</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q15</field>
+ <field name="info">
+Inflammatory bowel disease-26</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD2">
+ <field name="name">IBD2</field>
+ <field name="long_name">inflammatory bowel disease 2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.2-q24.1</field>
+ <field name="info">
+Inflammatory bowel disease-2 [MIM:266600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD3">
+ <field name="name">IBD3</field>
+ <field name="long_name">inflammatory bowel disease 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Inflammatory bowel disease-3 [MIM:266600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD4">
+ <field name="name">IBD4</field>
+ <field name="long_name">inflammatory bowel disease 4</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11-q12</field>
+ <field name="info">
+Inflammatory bowel disease-4 [MIM:266600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD5">
+ <field name="name">IBD5</field>
+ <field name="long_name">inflammatory bowel disease 5</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Inflammatory bowel disease-5 [MIM:266600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD6">
+ <field name="name">IBD6</field>
+ <field name="long_name">inflammatory bowel disease 6</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13</field>
+ <field name="info">
+Inflammatory bowel disease-6 [MIM:266600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD7">
+ <field name="name">IBD7</field>
+ <field name="long_name">inflammatory bowel disease 7</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Inflammatory bowel disease-7 [MIM:266600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD8">
+ <field name="name">IBD8</field>
+ <field name="long_name">inflammatory bowel disease 8</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p</field>
+ <field name="info">
+Inflammatory bowel disease-8 [MIM:266600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBD9">
+ <field name="name">IBD9</field>
+ <field name="long_name">inflammatory bowel disease 9</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26</field>
+ <field name="info">
+Inflammatory bowel disease-9 [MIM:266600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IBGC1">
+ <field name="name">IBGC1</field>
+ <field name="long_name">idiopathic basal ganglia calcification 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q</field>
+ <field name="info">
+Basal ganglia calcification, idiopathic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ICAM1">
+ <field name="name">ICAM1</field>
+ <field name="long_name">intercellular adhesion molecule 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3-p13.2</field>
+ <field name="info">
+Malaria, cerebral, susceptibility to [MIM:611162]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ICAM5">
+ <field name="name">ICAM5</field>
+ <field name="long_name">intercellular adhesion molecule 5, telencephalin</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ICCA">
+ <field name="name">ICCA</field>
+ <field name="long_name">infantile convulsions and paroxysmal choreoathetosis</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12-q12</field>
+ <field name="info">
+Convulsions, infantile and paroxysmal choreoathetosis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ICK">
+ <field name="name">ICK</field>
+ <field name="long_name">intestinal cell (MAK-like) kinase</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12.3</field>
+ <field name="info">
+Endocrine-cerebroosteodysplasia [MIM:612651]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ICOS">
+ <field name="name">ICOS</field>
+ <field name="long_name">inducible T-cell co-stimulator</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33</field>
+ <field name="info">
+ICOS deficiency [MIM:607594]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ICR2B">
+ <field name="name">ICR2B</field>
+ <field name="long_name">ichthyosis congenita II, lamellar ichthyosis B</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q34</field>
+ <field name="info">
+Ichthyosis, lamellar 2 [MIM:601277]
+Ichthyosis, harlequin [MIM:242500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM10">
+ <field name="name">IDDM10</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 10</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p15.1</field>
+ <field name="info">
+Interleukin-2 receptor, alpha chain, deficiency of [MIM:606367]
+Diabetes, mellitus, insulin-dependent, susceptibility to, 10 [MIM:601942]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM11">
+ <field name="name">IDDM11</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 11</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3-q31</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM12">
+ <field name="name">IDDM12</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 12</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33</field>
+ <field name="info">
+Graves disease, susceptibility to [MIM:275000]
+Hypothyroidism, autoimmune [MIM:140300]
+Diabetes mellitus, insulin-dependent, susceptibility to [MIM:601388]
+Celiac disease, susceptibility to [MIM:609755]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM13">
+ <field name="name">IDDM13</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 13</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q34</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 13</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM15">
+ <field name="name">IDDM15</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 15</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 15</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM17">
+ <field name="name">IDDM17</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 17</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q25</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 17</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM18">
+ <field name="name">IDDM18</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 18</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1-q33.1</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 18</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM20">
+ <field name="name">IDDM20</field>
+ <field name="long_name">Diabetes mellitus, insulin-dependent, 20</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 20</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM21">
+ <field name="name">IDDM21</field>
+ <field name="long_name">Diabetes mellitus, insulin-dependent, 21</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 21</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM23">
+ <field name="name">IDDM23</field>
+ <field name="long_name">Diabetes mellitus, insulin-dependent, 23</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q27</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 23</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM2">
+ <field name="name">IDDM2</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM3">
+ <field name="name">IDDM3</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 3</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM4">
+ <field name="name">IDDM4</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 4</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM5">
+ <field name="name">IDDM5</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 5</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 5 [MIM:600320]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM6">
+ <field name="name">IDDM6</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 6</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM7">
+ <field name="name">IDDM7</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 7</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDM8">
+ <field name="name">IDDM8</field>
+ <field name="long_name">insulin-dependent diabetes mellitus 8</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25-q27</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDDMX">
+ <field name="name">IDDMX</field>
+ <field name="long_name">Diabetes mellitus, insulin-dependent, X-linked, susceptibility to</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, X-linked</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDH1">
+ <field name="name">IDH1</field>
+ <field name="long_name">isocitrate dehydrogenase 1 (NADP+), soluble</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDH3B">
+ <field name="name">IDH3B</field>
+ <field name="long_name">isocitrate dehydrogenase 3 (NAD+) beta</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p13</field>
+ <field name="info">
+Retinitis pigmentosa-46</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDS">
+ <field name="name">IDS</field>
+ <field name="long_name">iduronate 2-sulfatase</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Mucopolysaccharidosis II</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IDUA">
+ <field name="name">IDUA</field>
+ <field name="long_name">iduronidase, alpha-L-</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.3</field>
+ <field name="info">
+Mucopolysaccharidosis Ih [MIM:607014]
+Mucopolysaccharidosis Is [MIM:607016]
+Mucopolysaccharidosis Ih/s [MIM:607015]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IFIH1">
+ <field name="name">IFIH1</field>
+ <field name="long_name">interferon induced with helicase C domain 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IFNA10">
+ <field name="name">IFNA10</field>
+ <field name="long_name">interferon, alpha 10</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IFNA17">
+ <field name="name">IFNA17</field>
+ <field name="long_name">interferon, alpha 17</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IFNA1">
+ <field name="name">IFNA1</field>
+ <field name="long_name">interferon, alpha 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p22</field>
+ <field name="info">
+Interferon, alpha, deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IFNA2">
+ <field name="name">IFNA2</field>
+ <field name="long_name">interferon, alpha 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IFNAR1">
+ <field name="name">IFNAR1</field>
+ <field name="long_name">interferon (alpha, beta and omega) receptor 1</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IFNAR2">
+ <field name="name">IFNAR2</field>
+ <field name="long_name">interferon (alpha, beta and omega) receptor 2</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.1</field>
+ <field name="info">
+Hepatitis B virus, susceptibility to [MIM:610424]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IFNGR1">
+ <field name="name">IFNGR1</field>
+ <field name="long_name">interferon gamma receptor 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23-q24</field>
+ <field name="info">
+Mycobacterial infection, atypical, familial disseminated [MIM:209950]
+BCG infection, generalized familial [MIM:209950]
+H. pylori infection, susceptibility to [MIM:600263]
+Tuberculosis, susceptibility to [MIM:607948]
+Mycobacterium tuberculosis infection, protection against [MIM:600263]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IFNGR2">
+ <field name="name">IFNGR2</field>
+ <field name="long_name">interferon gamma receptor 2 (interferon gamma transducer 1)</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.1-q22.2</field>
+ <field name="info">
+Mycobacterial infection, atypical, familial disseminated [MIM:209950]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IFNG">
+ <field name="name">IFNG</field>
+ <field name="long_name">interferon, gamma</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q14</field>
+ <field name="info">
+TSC2 angiomyolipomas, renal, modifier of [MIM:191100]
+Aplastic anemia [MIM:609135]
+Tuberculosis, protection against [MIM:607948]
+AIDS, rapid progression to [MIM:609423]
+Hepatitis C virus, resistance to [MIM:609532]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IFT80">
+ <field name="name">IFT80</field>
+ <field name="long_name">intraflagellar transport 80 homolog (Chlamydomonas)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q24-q26</field>
+ <field name="info">
+Asphyxiating thoracic dystrophy 2 [MIM:611263]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGAD1">
+ <field name="name">IGAD1</field>
+ <field name="long_name">immunoglobulin A (IgA) deficiency susceptibility 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Immunoglobulin A deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGBP1">
+ <field name="name">IGBP1</field>
+ <field name="long_name">immunoglobulin (CD79A) binding protein 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.1-q13.3</field>
+ <field name="info">
+Corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia [MIM:300472]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGES">
+ <field name="name">IGES</field>
+ <field name="long_name">immunoglobulin E concentration, serum</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1</field>
+ <field name="info">
+Allergy and asthma susceptibility</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGF1R">
+ <field name="name">IGF1R</field>
+ <field name="long_name">insulin-like growth factor 1 receptor</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q25-q26</field>
+ <field name="info">
+Insulin-like growth factor I, resistance to [MIM:270450]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGF1">
+ <field name="name">IGF1</field>
+ <field name="long_name">insulin-like growth factor 1 (somatomedin C)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q22-q24.1</field>
+ <field name="info">
+Growth retardation with deafness and mental retardation due to IGF1 deficiency [MIM:608747]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGF2BP2">
+ <field name="name">IGF2BP2</field>
+ <field name="long_name">insulin-like growth factor 2 mRNA binding protein 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q28</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent, susceptibility to [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGF2R">
+ <field name="name">IGF2R</field>
+ <field name="long_name">insulin-like growth factor 2 receptor</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q26</field>
+ <field name="info">
+Hepatocellular carcinoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGF2">
+ <field name="name">IGF2</field>
+ <field name="long_name">insulin-like growth factor 2 (somatomedin A)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Intrauterine and postnatal growth retardation</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGFALS">
+ <field name="name">IGFALS</field>
+ <field name="long_name">insulin-like growth factor binding protein, acid labile subunit</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+Acid-labile subunit, deficiency of</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGFBP1">
+ <field name="name">IGFBP1</field>
+ <field name="long_name">insulin-like growth factor binding protein 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGFBP3">
+ <field name="name">IGFBP3</field>
+ <field name="long_name">insulin-like growth factor binding protein 3</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGFBP5">
+ <field name="name">IGFBP5</field>
+ <field name="long_name">insulin-like growth factor binding protein 5</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33-q36</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGHA1">
+ <field name="name">IGHA1</field>
+ <field name="long_name">immunoglobulin heavy constant alpha 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.33</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGHG1">
+ <field name="name">IGHG1</field>
+ <field name="long_name">immunoglobulin heavy constant gamma 1 (G1m marker)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.33</field>
+ <field name="info">
+infections,recurrent</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGHG2">
+ <field name="name">IGHG2</field>
+ <field name="long_name">immunoglobulin heavy constant gamma 2 (G2m marker)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.33</field>
+ <field name="info">
+IgG2 deficiency, selective</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGHG4">
+ <field name="name">IGHG4</field>
+ <field name="long_name">immunoglobulin heavy constant gamma 4 (G4m marker)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.33</field>
+ <field name="info">
+immunoglobulin,gamma 4 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGHMBP2">
+ <field name="name">IGHMBP2</field>
+ <field name="long_name">immunoglobulin mu binding protein 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.2-q13.4</field>
+ <field name="info">
+Neuronopathy, distal hereditary motor, type VI [MIM:604320]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGHM">
+ <field name="name">IGHM</field>
+ <field name="long_name">immunoglobulin heavy constant mu</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.33</field>
+ <field name="info">
+Agammaglobulinemia [MIM:601495]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGHR">
+ <field name="name">IGHR</field>
+ <field name="long_name">immunoglobulin heavy chain regulator</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.33</field>
+ <field name="info">
+Hyperimmunoglobulin G1 syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGKC">
+ <field name="name">IGKC</field>
+ <field name="long_name">immunoglobulin kappa constant</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p12</field>
+ <field name="info">
+Kappa light chain deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGKV@">
+ <field name="name">IGKV@</field>
+ <field name="long_name">immunoglobulin kappa variable group</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IGLL1">
+ <field name="name">IGLL1</field>
+ <field name="long_name">immunoglobulin lambda-like polypeptide 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.21</field>
+ <field name="info">
+Agammaglobulinemia, autosomal recessive [MIM:601495]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IHH">
+ <field name="name">IHH</field>
+ <field name="long_name">Indian hedgehog homolog (Drosophila)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33-q35</field>
+ <field name="info">
+Acrocapitofemoral dysplasia [MIM:607778]
+Brachydactyly, type A1 [MIM:112500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IHPS2">
+ <field name="name">IHPS2</field>
+ <field name="long_name">Pyloric stenosis, infantile hypertrophic, 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13-p12</field>
+ <field name="info">
+Pyloric stenosis, infantile hypertrophic, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IHPS3">
+ <field name="name">IHPS3</field>
+ <field name="long_name">Pyloric stenosis, infantile hypertrophic, 3</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q14-q22</field>
+ <field name="info">
+Pyloric stenosis, infantile hypertrophic, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IHPS4">
+ <field name="name">IHPS4</field>
+ <field name="long_name">Pyloric stenosis, infantile hypertrophic, 4</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq23</field>
+ <field name="info">
+Pyloric stenosis, infantile hypertrophic, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IHPS5">
+ <field name="name">IHPS5</field>
+ <field name="long_name">Pyloric stenosis, infantile hypertrophic, 5</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.3</field>
+ <field name="info">
+Pyloric stenosis, infantile hypertrophic, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IH">
+ <field name="name">IH</field>
+ <field name="long_name">Hemihypertrophy</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15</field>
+ <field name="info">
+Hemihypertrophy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IKBKAP">
+ <field name="name">IKBKAP</field>
+ <field name="long_name">inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q31</field>
+ <field name="info">
+Dysautonomia, familial [MIM:223900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IKBKG">
+ <field name="name">IKBKG</field>
+ <field name="long_name">inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Incontinentia pigmenti, type II [MIM:308300]
+Ectodermal dysplasia, hypohidrotic, with immune deficiency [MIM:300291]
+Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency [MIM:300301]
+Immunodeficiency, isolated [MIM:300584]
+Atypical mycobacteriosis, familial [MIM:300636]
+Invasive pneumococcal disease, recurrent isolated, 2 [MIM:300640]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IKZF1">
+ <field name="name">IKZF1</field>
+ <field name="long_name">IKAROS family zinc finger 1 (Ikaros)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p12</field>
+ <field name="info">
+Leukemia, acute lymphoblastic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL10RA">
+ <field name="name">IL10RA</field>
+ <field name="long_name">interleukin 10 receptor, alpha</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL10">
+ <field name="name">IL10</field>
+ <field name="long_name">interleukin 10</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31-q32</field>
+ <field name="info">
+HIV-1, susceptibility to
+Graft-versus-host disease, protection against
+Rheumatoid arthritis, progression of [MIM:180300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL12A">
+ <field name="name">IL12A</field>
+ <field name="long_name">interleukin 12A (natural killer cell stimulatory factor 1, cytotoxic lymphocyte maturation factor 1, p35)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p12-q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL12B">
+ <field name="name">IL12B</field>
+ <field name="long_name">interleukin 12B (natural killer cell stimulatory factor 2, cytotoxic lymphocyte maturation factor 2, p40)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1-q33.1</field>
+ <field name="info">
+BCG and salmonella infection, disseminated [MIM:209950]
+Asthma, susceptibility to [MIM:600807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL12RB1">
+ <field name="name">IL12RB1</field>
+ <field name="long_name">interleukin 12 receptor, beta 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.1</field>
+ <field name="info">
+Mycobacterial and salmonella infections, susceptibility to [MIM:209950]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL12RB2">
+ <field name="name">IL12RB2</field>
+ <field name="long_name">interleukin 12 receptor, beta 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL13">
+ <field name="name">IL13</field>
+ <field name="long_name">interleukin 13</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Asthma, susceptibility to [MIM:600807]
+Allergic rhinitis, susceptibility to [MIM:607154]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL16">
+ <field name="name">IL16</field>
+ <field name="long_name">interleukin 16 (lymphocyte chemoattractant factor)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL17F">
+ <field name="name">IL17F</field>
+ <field name="long_name">interleukin 17F</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL17RB">
+ <field name="name">IL17RB</field>
+ <field name="long_name">interleukin 17 receptor B</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL18RAP">
+ <field name="name">IL18RAP</field>
+ <field name="long_name">interleukin 18 receptor accessory protein</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL18">
+ <field name="name">IL18</field>
+ <field name="long_name">interleukin 18 (interferon-gamma-inducing factor)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22.2-q22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL1A">
+ <field name="name">IL1A</field>
+ <field name="long_name">interleukin 1, alpha</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL1B">
+ <field name="name">IL1B</field>
+ <field name="long_name">interleukin 1, beta</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14</field>
+ <field name="info">
+Gastric cancer risk after H. pylori infection [MIM:137215]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL1R1">
+ <field name="name">IL1R1</field>
+ <field name="long_name">interleukin 1 receptor, type I</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL1RAPL1">
+ <field name="name">IL1RAPL1</field>
+ <field name="long_name">interleukin 1 receptor accessory protein-like 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.1-p21.3</field>
+ <field name="info">
+Mental retardation, X-linked, 21/34 [MIM:300143]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL1RN">
+ <field name="name">IL1RN</field>
+ <field name="long_name">interleukin 1 receptor antagonist</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14.2</field>
+ <field name="info">
+Gastric cancer risk after H. pylori infection [MIM:137215]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL21R">
+ <field name="name">IL21R</field>
+ <field name="long_name">interleukin 21 receptor</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p11</field>
+ <field name="info">
+Lymphoma, diffuse large B-cell
+IgE, elevated level of [MIM:147050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL23R">
+ <field name="name">IL23R</field>
+ <field name="long_name">interleukin 23 receptor</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31.1</field>
+ <field name="info">
+Crohn disease, ileal, protection against [MIM:612261]
+Psoriasis, protection against [MIM:177900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL2RA">
+ <field name="name">IL2RA</field>
+ <field name="long_name">interleukin 2 receptor, alpha</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p15.1</field>
+ <field name="info">
+Interleukin-2 receptor, alpha chain, deficiency of [MIM:606367]
+Diabetes, mellitus, insulin-dependent, susceptibility to, 10 [MIM:601942]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL2RG">
+ <field name="name">IL2RG</field>
+ <field name="long_name">interleukin 2 receptor, gamma (severe combined immunodeficiency)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13</field>
+ <field name="info">
+Severe combined immunodeficiency, X-linked [MIM:300400]
+Combined immunodeficiency, X-linked, moderate [MIM:312863]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL2">
+ <field name="name">IL2</field>
+ <field name="long_name">interleukin 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q26-q27</field>
+ <field name="info">
+Severe combined immunodeficiency due to IL2 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL3">
+ <field name="name">IL3</field>
+ <field name="long_name">interleukin 3 (colony-stimulating factor, multiple)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1</field>
+ <field name="info">
+leukemia,acute,lymphoblastic,preB cell,with translocation t(5;14)(q31;q32)</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL4R">
+ <field name="name">IL4R</field>
+ <field name="long_name">interleukin 4 receptor</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12.1-p11.2</field>
+ <field name="info">
+Atopy, susceptibility to [MIM:147050]
+AIDS, slow progression to [MIM:609423]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL4">
+ <field name="name">IL4</field>
+ <field name="long_name">interleukin 4</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL6R">
+ <field name="name">IL6R</field>
+ <field name="long_name">interleukin 6 receptor</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL6">
+ <field name="name">IL6</field>
+ <field name="long_name">interleukin 6 (interferon, beta 2)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p21</field>
+ <field name="info">
+Rheumatoid arthritis, systemic juvenile [MIM:604302]
+Kaposi sarcoma, susceptibility to [MIM:148000]
+Diabetes, susceptibility to, 222100 [MIM:125853]
+Intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to [MIM:108010]
+Crohn disease-associated growth failure [MIM:266600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL7R">
+ <field name="name">IL7R</field>
+ <field name="long_name">interleukin 7 receptor</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13</field>
+ <field name="info">
+Severe combined immunodeficiency, T-cell negative, B-cell/natural killer cell-positive type [MIM:608971]
+Multiple sclerosis, susceptibility to [MIM:126200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL7">
+ <field name="name">IL7</field>
+ <field name="long_name">interleukin 7</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q12-q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL8RA">
+ <field name="name">IL8RA</field>
+ <field name="long_name">interleukin 8 receptor, alpha</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35</field>
+ <field name="info">
+AIDS, slow progression to [MIM:609423]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL8">
+ <field name="name">IL8</field>
+ <field name="long_name">interleukin 8</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q12-q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IL9">
+ <field name="name">IL9</field>
+ <field name="long_name">interleukin 9</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ILK">
+ <field name="name">ILK</field>
+ <field name="long_name">integrin-linked kinase</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5-p15.4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IMAGE">
+ <field name="name">IMAGE</field>
+ <field name="long_name">Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies</field>
+ <field name="chromosome">X</field>
+ <field name="location">X</field>
+ <field name="info">
+IMAGE syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IMPA2">
+ <field name="name">IMPA2</field>
+ <field name="long_name">inositol(myo)-1(or 4)-monophosphatase 2</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IMPDH1">
+ <field name="name">IMPDH1</field>
+ <field name="long_name">IMP (inosine monophosphate) dehydrogenase 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31.3-q32</field>
+ <field name="info">
+Retinitis pigmentosa-10 [MIM:180105]
+Leber congenital amaurosis 11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IMPDH2">
+ <field name="name">IMPDH2</field>
+ <field name="long_name">IMP (inosine monophosphate) dehydrogenase 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.2</field>
+ <field name="info">
+IMPDH2 enzyme activity, variation in</field>
+</record>
+<record model="gnuhealth.disease.gene" id="INDX">
+ <field name="name">INDX</field>
+ <field name="long_name">Immunoneurologic syndrome X-linked, of Wood, Black, and Norbury</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26-qter</field>
+ <field name="info">
+Wood neuroimmunologic syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ING1">
+ <field name="name">ING1</field>
+ <field name="long_name">inhibitor of growth family, member 1</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q34</field>
+ <field name="info">
+Squamous cell carcinoma, head and neck [MIM:275355]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="INHA">
+ <field name="name">INHA</field>
+ <field name="long_name">inhibin, alpha</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33-q36</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="INLNE">
+ <field name="name">INLNE</field>
+ <field name="long_name">Ichthyosis, nonlamellar and nonerythrodermic, congenital, autosomal recessive</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2-p13.1</field>
+ <field name="info">
+Ichthyosis, nonlamellar and nonerythrodermic, congenital</field>
+</record>
+<record model="gnuhealth.disease.gene" id="INPP4A">
+ <field name="name">INPP4A</field>
+ <field name="long_name">inositol polyphosphate-4-phosphatase, type I, 107kDa</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="INSIG2">
+ <field name="name">INSIG2</field>
+ <field name="long_name">insulin induced gene 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="INSL3">
+ <field name="name">INSL3</field>
+ <field name="long_name">insulin-like 3 (Leydig cell)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2</field>
+ <field name="info">
+Cryptorchidism, idiopathic [MIM:219050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="INSR">
+ <field name="name">INSR</field>
+ <field name="long_name">insulin receptor</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2</field>
+ <field name="info">
+Leprechaunism [MIM:246200]
+Rabson-Mendenhall syndrome [MIM:262190]
+Diabetes mellitus, insulin-resistant, with acanthosis nigricans [MIM:610549]
+Hyperinsulinemic hypoglycemia, familial, 5 [MIM:609968]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="INS">
+ <field name="name">INS</field>
+ <field name="long_name">insulin</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Hyperproinsulinemia, familial, with or without diabetes</field>
+</record>
+<record model="gnuhealth.disease.gene" id="INVS">
+ <field name="name">INVS</field>
+ <field name="long_name">inversin</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q31</field>
+ <field name="info">
+Nephronophthisis 2, infantile [MIM:602088]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IPOX">
+ <field name="name">IPOX</field>
+ <field name="long_name">Intestinal pseudoobstruction, neuronal, primary idiopathic</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Intestinal pseudoobstruction, neuronal, X-linked</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IQCB1">
+ <field name="name">IQCB1</field>
+ <field name="long_name">IQ motif containing B1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21.1</field>
+ <field name="info">
+Senior-Loken syndrome 5 [MIM:609254]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IRAK1">
+ <field name="name">IRAK1</field>
+ <field name="long_name">interleukin-1 receptor-associated kinase 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IRAK3">
+ <field name="name">IRAK3</field>
+ <field name="long_name">interleukin-1 receptor-associated kinase 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q14.3</field>
+ <field name="info">
+Asthma susceptibility 5 [MIM:611064]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IRAK4">
+ <field name="name">IRAK4</field>
+ <field name="long_name">interleukin-1 receptor-associated kinase 4</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q12</field>
+ <field name="info">
+IRAK4 deficiency [MIM:607676]
+Invasive pneumococcal disease, recurrent isolated, 1 [MIM:610799]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IRF1">
+ <field name="name">IRF1</field>
+ <field name="long_name">interferon regulatory factor 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1</field>
+ <field name="info">
+Macrocytic anemia, refractory, of 5q- syndrome [MIM:153550]
+Myelodysplastic syndrome, preleukemic
+Myelogenous leukemia, acute
+Gastric cancer [MIM:137215]
+Nonsmall cell lung cancer</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IRF2">
+ <field name="name">IRF2</field>
+ <field name="long_name">interferon regulatory factor 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q35.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IRF4">
+ <field name="name">IRF4</field>
+ <field name="long_name">interferon regulatory factor 4</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p25-p23</field>
+ <field name="info">
+Multiple myeloma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IRF5">
+ <field name="name">IRF5</field>
+ <field name="long_name">interferon regulatory factor 5</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q32</field>
+ <field name="info">
+Inflammatory bowel disease 14, susceptibility to [MIM:612245]
+Systemic lupus erythematosus, susceptibility to, 10 [MIM:612251]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IRF6">
+ <field name="name">IRF6</field>
+ <field name="long_name">interferon regulatory factor 6</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32-q41</field>
+ <field name="info">
+van der Woude syndrome [MIM:119300]
+Popliteal pterygium syndrome [MIM:119500]
+Orofacial cleft 6 [MIM:608864]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IRGM">
+ <field name="name">IRGM</field>
+ <field name="long_name">immunity-related GTPase family, M</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q33.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="IRS1">
+ <field name="name">IRS1</field>
+ <field name="long_name">insulin receptor substrate 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q36</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent [MIM:125853]
+Coronary artery disease, susceptibility to (3) 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IRS2">
+ <field name="name">IRS2</field>
+ <field name="long_name">insulin receptor substrate 2</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q34</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IS2">
+ <field name="name">IS2</field>
+ <field name="long_name">Scoliosis, idiopathic 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+Scoliosis, idiopathic 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IS4">
+ <field name="name">IS4</field>
+ <field name="long_name">Scoliosis, idiopathic, susceptibility to, 4</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q31.2-q34.2</field>
+ <field name="info">
+Scoliosis, idiopathic, susceptibility to, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ISCU">
+ <field name="name">ISCU</field>
+ <field name="long_name">iron-sulfur cluster scaffold homolog (E. coli)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.1</field>
+ <field name="info">
+Myopathy with exercise intolerance, Swedish type [MIM:255125]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ISL1">
+ <field name="name">ISL1</field>
+ <field name="long_name">ISL LIM homeobox 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ISYNA1">
+ <field name="name">ISYNA1</field>
+ <field name="long_name">inositol-3-phosphate synthase 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITC1">
+ <field name="name">ITC1</field>
+ <field name="long_name">unknown</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q22</field>
+ <field name="info">
+Hypertrichosis universalis congenita, Ambras type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITGA11">
+ <field name="name">ITGA11</field>
+ <field name="long_name">integrin, alpha 11</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22.3-q23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITGA2B">
+ <field name="name">ITGA2B</field>
+ <field name="long_name">integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.32</field>
+ <field name="info">
+Glanzmann thrombasthenia, type A [MIM:273800]
+Thrombocytopenia, neonatal alloimmune</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITGA2">
+ <field name="name">ITGA2</field>
+ <field name="long_name">integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q23-q31</field>
+ <field name="info">
+Neonatal alloimmune thrombocytopenia
+Glycoprotein Ia deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITGA6">
+ <field name="name">ITGA6</field>
+ <field name="long_name">integrin, alpha 6</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31.1</field>
+ <field name="info">
+Epidermolysis bullosa, junctional, with pyloric stenosis [MIM:226730]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITGA7">
+ <field name="name">ITGA7</field>
+ <field name="long_name">integrin, alpha 7</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Myopathy, congenital</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITGAM">
+ <field name="name">ITGAM</field>
+ <field name="long_name">integrin, alpha M (complement component 3 receptor 3 subunit)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p11.2</field>
+ <field name="info">
+Systemic lupus erythematous, association with susceptibility to, 6 [MIM:609939]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITGB2">
+ <field name="name">ITGB2</field>
+ <field name="long_name">integrin, beta 2 (complement component 3 receptor 3 and 4 subunit)</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Leukocyte adhesion deficiency [MIM:116920]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITGB3">
+ <field name="name">ITGB3</field>
+ <field name="long_name">integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.32</field>
+ <field name="info">
+Glanzmann thrombasthenia, type B</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITGB4">
+ <field name="name">ITGB4</field>
+ <field name="long_name">integrin, beta 4</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11-qter</field>
+ <field name="info">
+Epidermolysis bullosa, junctional, with pyloric atresia [MIM:226730]
+Epidermolysis bullosa, junctional, non-Herlitz type [MIM:226650]
+Epidermolysis bullosa of hands and feet [MIM:131800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITIH1">
+ <field name="name">ITIH1</field>
+ <field name="long_name">inter-alpha (globulin) inhibitor H1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.2-p21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITIH3">
+ <field name="name">ITIH3</field>
+ <field name="long_name">inter-alpha (globulin) inhibitor H3</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.2-p21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITIH4">
+ <field name="name">ITIH4</field>
+ <field name="long_name">inter-alpha (globulin) inhibitor H4 (plasma Kallikrein-sensitive glycoprotein)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.2-p14.1</field>
+ <field name="info">
+Hypercholesterolemia, susceptibility to [MIM:143890]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITM2B">
+ <field name="name">ITM2B</field>
+ <field name="long_name">integral membrane protein 2B</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14</field>
+ <field name="info">
+Dementia, familial British [MIM:176500]
+Dementia, familial Danish [MIM:117300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITPA">
+ <field name="name">ITPA</field>
+ <field name="long_name">inosine triphosphatase (nucleoside triphosphate pyrophosphatase)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p</field>
+ <field name="info">
+Inosine triphosphatase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITPKC">
+ <field name="name">ITPKC</field>
+ <field name="long_name">inositol 1,4,5-trisphosphate 3-kinase C</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+Kawasaki disease, susceptibility to [MIM:611775]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITPR1">
+ <field name="name">ITPR1</field>
+ <field name="long_name">inositol 1,4,5-triphosphate receptor, type 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26-p25</field>
+ <field name="info">
+Spinocerebellar ataxia 15 [MIM:606658]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITPR3">
+ <field name="name">ITPR3</field>
+ <field name="long_name">inositol 1,4,5-triphosphate receptor, type 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6pter-p21</field>
+ <field name="info">
+Diabetes, type 1, susceptibility to [MIM:222100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ITS">
+ <field name="name">ITS</field>
+ <field name="long_name">Insulinoma tumor suppressor gene locus</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.1-q12.2</field>
+ <field name="info">
+Insulinoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IVD">
+ <field name="name">IVD</field>
+ <field name="long_name">isovaleryl Coenzyme A dehydrogenase</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q14-q15</field>
+ <field name="info">
+Isovaleric acidemia [MIM:243500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IV">
+ <field name="name">IV</field>
+ <field name="long_name">inversus situs, viscerum</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22.3</field>
+ <field name="info">
+Leiomyomatosis, diffuse, with Alport syndrome [MIM:308940]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="IYD">
+ <field name="name">IYD</field>
+ <field name="long_name">iodotyrosine deiodinase</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q24-q25</field>
+ <field name="info">
+Thyroid hormonogenesis, genetic defect in, 4 [MIM:274800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="JAG1">
+ <field name="name">JAG1</field>
+ <field name="long_name">jagged 1 (Alagille syndrome)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p12</field>
+ <field name="info">
+Alagille syndrome [MIM:118450]
+Tetralogy of Fallot [MIM:187500]
+Deafness, congenital heart defects, and posterior embryotoxon</field>
+</record>
+<record model="gnuhealth.disease.gene" id="JAG2">
+ <field name="name">JAG2</field>
+ <field name="long_name">jagged 2</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="JAK2">
+ <field name="name">JAK2</field>
+ <field name="long_name">Janus kinase 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p24</field>
+ <field name="info">
+Polycythemia vera [MIM:263300]
+Thrombocythemia, essential [MIM:187950]
+Myelofibrosis, idiopathic [MIM:254450]
+Budd-Chiari syndrome [MIM:600880]
+Leukemia, acute myelogenous [MIM:601626]
+Myeloproliferative disorder with erythrocytosis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="JAK3">
+ <field name="name">JAK3</field>
+ <field name="long_name">Janus kinase 3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.1</field>
+ <field name="info">
+SCID, autosomal recessive, T-negative/B-positive type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="JAWAD">
+ <field name="name">JAWAD</field>
+ <field name="long_name">Microcephaly with digital anomalies</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.22-q11.2</field>
+ <field name="info">
+Microcephaly with digital anomalies</field>
+</record>
+<record model="gnuhealth.disease.gene" id="JAZF1">
+ <field name="name">JAZF1</field>
+ <field name="long_name">JAZF zinc finger 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15</field>
+ <field name="info">
+Endometrial stromal tumors</field>
+</record>
+<record model="gnuhealth.disease.gene" id="JBS">
+ <field name="name">JBS</field>
+ <field name="long_name">Jacobsen syndrome</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Jacobsen syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="JBTS1">
+ <field name="name">JBTS1</field>
+ <field name="long_name">Joubert syndrome 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.3</field>
+ <field name="info">
+Joubert syndrome-1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="JPD">
+ <field name="name">JPD</field>
+ <field name="long_name">juvenile periodontitis</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q14.1-q14.3</field>
+ <field name="info">
+Papillon-Lefevre syndrome [MIM:245000]
+Haim-Munk syndrome [MIM:245010]
+Periodontitis, juvenile [MIM:170650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="JPH2">
+ <field name="name">JPH2</field>
+ <field name="long_name">junctophilin 2</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="JPH3">
+ <field name="name">JPH3</field>
+ <field name="long_name">junctophilin 3</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.3</field>
+ <field name="info">
+Huntington disease-like 2 [MIM:606438]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="JRK">
+ <field name="name">JRK</field>
+ <field name="long_name">jerky homolog (mouse)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24</field>
+ <field name="info">
+Epilepsy, childhood absence, evolving to juvenile myoclonic epilepsy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="JUP">
+ <field name="name">JUP</field>
+ <field name="long_name">junction plakoglobin</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+Naxos disease [MIM:601214]
+Arrhythmogenic right ventricular dysplasia, familial, 12 [MIM:611528]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KAL1">
+ <field name="name">KAL1</field>
+ <field name="long_name">Kallmann syndrome 1 sequence</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3</field>
+ <field name="info">
+Kallmann syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KAL3">
+ <field name="name">KAL3</field>
+ <field name="long_name">Kallmann syndrome 3 (autosomal dominant)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p13</field>
+ <field name="info">
+Kallmann syndrome 3 [MIM:244200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KAZA">
+ <field name="name">KAZA</field>
+ <field name="long_name">Kala-azar (visceral leishmaniasis), susceptibility to</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12</field>
+ <field name="info">
+Kala-azar, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNA1">
+ <field name="name">KCNA1</field>
+ <field name="long_name">potassium voltage-gated channel, shaker-related subfamily, member 1 (episodic ataxia with myokymia)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+Episodic ataxia/myokymia syndrome [MIM:160120]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNA3">
+ <field name="name">KCNA3</field>
+ <field name="long_name">potassium voltage-gated channel, shaker-related subfamily, member 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p21-p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNA5">
+ <field name="name">KCNA5</field>
+ <field name="long_name">potassium voltage-gated channel, shaker-related subfamily, member 5</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+Atrial fibrillation, familial, 7 [MIM:612240]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNAB2">
+ <field name="name">KCNAB2</field>
+ <field name="long_name">potassium voltage-gated channel, shaker-related subfamily, beta member 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNC3">
+ <field name="name">KCNC3</field>
+ <field name="long_name">potassium voltage-gated channel, Shaw-related subfamily, member 3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3-q13.4</field>
+ <field name="info">
+Spinocerebellar ataxia-13 [MIM:605259]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCND2">
+ <field name="name">KCND2</field>
+ <field name="long_name">potassium voltage-gated channel, Shal-related subfamily, member 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNE1L">
+ <field name="name">KCNE1L</field>
+ <field name="long_name">KCNE1-like</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNE1">
+ <field name="name">KCNE1</field>
+ <field name="long_name">potassium voltage-gated channel, Isk-related family, member 1</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.1-q22.2</field>
+ <field name="info">
+Jervell and Lange-Nielsen syndrome 2 [MIM:612347]
+Long QT syndrome-5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNE2">
+ <field name="name">KCNE2</field>
+ <field name="long_name">potassium voltage-gated channel, Isk-related family, member 2</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.1</field>
+ <field name="info">
+Long QT syndrome-6
+Atrial fibrillation, familial, 4 [MIM:611493]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNE3">
+ <field name="name">KCNE3</field>
+ <field name="long_name">potassium voltage-gated channel, Isk-related family, member 3</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13-q14</field>
+ <field name="info">
+Hypokalemic periodic paralysis [MIM:170400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNE4">
+ <field name="name">KCNE4</field>
+ <field name="long_name">potassium voltage-gated channel, Isk-related family, member 4</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35-q36</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNH2">
+ <field name="name">KCNH2</field>
+ <field name="long_name">potassium voltage-gated channel, subfamily H (eag-related), member 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q35-q36</field>
+ <field name="info">
+Long QT syndrome-2
+Long QT syndrome, acquired, susceptibility to
+Short QT syndrome-1 [MIM:609620]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNJ10">
+ <field name="name">KCNJ10</field>
+ <field name="long_name">potassium inwardly-rectifying channel, subfamily J, member 10</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23.2</field>
+ <field name="info">
+SESAME syndrome [MIM:612780]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNJ11">
+ <field name="name">KCNJ11</field>
+ <field name="long_name">potassium inwardly-rectifying channel, subfamily J, member 11</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.1</field>
+ <field name="info">
+Hyperinsulinemic hypoglycemia, familial, 2 [MIM:601820]
+Diabetes, permanent neonatal [MIM:606176]
+Diabetes mellitus, permanent neonatal, with neurologic features [MIM:606176]
+Diabetes mellitus, type 2, susceptibility to [MIM:125853]
+Diabetes mellitus, transient neonatal, 3 [MIM:610582]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNJ13">
+ <field name="name">KCNJ13</field>
+ <field name="long_name">potassium inwardly-rectifying channel, subfamily J, member 13</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37</field>
+ <field name="info">
+Snowflake vitreoretinal degeneration [MIM:193230]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNJ15">
+ <field name="name">KCNJ15</field>
+ <field name="long_name">potassium inwardly-rectifying channel, subfamily J, member 15</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNJ1">
+ <field name="name">KCNJ1</field>
+ <field name="long_name">potassium inwardly-rectifying channel, subfamily J, member 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q24</field>
+ <field name="info">
+Bartter syndrome, type 2 [MIM:241200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNJ2">
+ <field name="name">KCNJ2</field>
+ <field name="long_name">potassium inwardly-rectifying channel, subfamily J, member 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23.1-q24.2</field>
+ <field name="info">
+Long QT syndrome-7 [MIM:170390]
+Short QT syndrome-3 [MIM:609622]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNJ8">
+ <field name="name">KCNJ8</field>
+ <field name="long_name">potassium inwardly-rectifying channel, subfamily J, member 8</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p11.23</field>
+ <field name="info">
+Prinzmetal angina</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNK6">
+ <field name="name">KCNK6</field>
+ <field name="long_name">potassium channel, subfamily K, member 6</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNK9">
+ <field name="name">KCNK9</field>
+ <field name="long_name">potassium channel, subfamily K, member 9</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.1-q24.3</field>
+ <field name="info">
+Birk-Barel mental retardation dysmorphism syndrome [MIM:612292]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNMA1">
+ <field name="name">KCNMA1</field>
+ <field name="long_name">potassium large conductance calcium-activated channel, subfamily M, alpha member 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.3</field>
+ <field name="info">
+Generalized epilepsy and paroxysmal dyskinesia [MIM:609446]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNMB1">
+ <field name="name">KCNMB1</field>
+ <field name="long_name">potassium large conductance calcium-activated channel, subfamily M, beta member 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q34</field>
+ <field name="info">
+Hypertension, diastolic, resistance to [MIM:608622]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNMB3">
+ <field name="name">KCNMB3</field>
+ <field name="long_name">potassium large conductance calcium-activated channel, subfamily M beta member 3</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.3-q27.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNN3">
+ <field name="name">KCNN3</field>
+ <field name="long_name">potassium intermediate/small conductance calcium-activated channel, subfamily N, member 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNQ1">
+ <field name="name">KCNQ1</field>
+ <field name="long_name">potassium voltage-gated channel, KQT-like subfamily, member 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Long QT syndrome-1 [MIM:192500]
+Jervell and Lange-Nielsen syndrome [MIM:220400]
+Atrial fibrillation, familial, 3 [MIM:607554]
+Torsades de pointes, drug-associated
+Short QT syndrome-2 [MIM:609621]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNQ2">
+ <field name="name">KCNQ2</field>
+ <field name="long_name">potassium voltage-gated channel, KQT-like subfamily, member 2</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.3</field>
+ <field name="info">
+Epilepsy, benign, neonatal, type 1 [MIM:121200]
+Myokymia with neonatal epilepsy [MIM:606437]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNQ3">
+ <field name="name">KCNQ3</field>
+ <field name="long_name">potassium voltage-gated channel, KQT-like subfamily, member 3</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24</field>
+ <field name="info">
+Epilepsy, benign neonatal, type 2 [MIM:121201]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNQ4">
+ <field name="name">KCNQ4</field>
+ <field name="long_name">potassium voltage-gated channel, KQT-like subfamily, member 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34</field>
+ <field name="info">
+Deafness, autosomal dominant 2A [MIM:600101]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNS3">
+ <field name="name">KCNS3</field>
+ <field name="long_name">potassium voltage-gated channel, delayed-rectifier, subfamily S, member 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCNV2">
+ <field name="name">KCNV2</field>
+ <field name="long_name">potassium channel, subfamily V, member 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p24.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCS">
+ <field name="name">KCS</field>
+ <field name="long_name">Kenny-Caffey syndrome</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42-q43</field>
+ <field name="info">
+Kenny-Caffey syndrome-1 [MIM:244460]
+Hypoparathyroidism-retardation-dysmorphism syndrome [MIM:241410]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KCTD7">
+ <field name="name">KCTD7</field>
+ <field name="long_name">potassium channel tetramerisation domain containing 7</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.21</field>
+ <field name="info">
+Epilepsy, progressive myoclonic 3 [MIM:611726]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KDR">
+ <field name="name">KDR</field>
+ <field name="long_name">kinase insert domain receptor (a type III receptor tyrosine kinase)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q12</field>
+ <field name="info">
+Hemangioma, capillary infantile, somatic [MIM:602089]
+Hemangioma, capillary infantile, susceptibility to [MIM:602089]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KEL">
+ <field name="name">KEL</field>
+ <field name="long_name">Kell blood group, metallo-endopeptidase</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q33</field>
+ <field name="info">
+Blood group, Kell</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KERA">
+ <field name="name">KERA</field>
+ <field name="long_name">keratocan</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q22</field>
+ <field name="info">
+Cornea plana congenita, recessive [MIM:217300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KFM">
+ <field name="name">KFM</field>
+ <field name="long_name">Klippel-Feil malformation</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q11.2</field>
+ <field name="info">
+Klippel-Feil syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KFSD">
+ <field name="name">KFSD</field>
+ <field name="long_name">keratosis follicularis spinulosa decalvans</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.1</field>
+ <field name="info">
+Keratosis follicularis spinulosa decalvans [MIM:308800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KHK">
+ <field name="name">KHK</field>
+ <field name="long_name">ketohexokinase (fructokinase)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p23.3-p23.2</field>
+ <field name="info">
+Fructosuria</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIAA0196">
+ <field name="name">KIAA0196</field>
+ <field name="long_name">KIAA0196</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.13</field>
+ <field name="info">
+Spastic paraplegia-8 [MIM:603563]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIAA0319">
+ <field name="name">KIAA0319</field>
+ <field name="long_name">KIAA0319</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p22.2</field>
+ <field name="info">
+Dyslexia, susceptibility to, 2 [MIM:600202]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIAA0513">
+ <field name="name">KIAA0513</field>
+ <field name="long_name">KIAA0513</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIAA1199">
+ <field name="name">KIAA1199</field>
+ <field name="long_name">KIAA1199</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q24</field>
+ <field name="info">
+Deafness, nonsyndromic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIAA1279">
+ <field name="name">KIAA1279</field>
+ <field name="long_name">KIAA1279</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.1</field>
+ <field name="info">
+Goldberg-Shprintzen megacolon syndrome [MIM:609460]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIF1B">
+ <field name="name">KIF1B</field>
+ <field name="long_name">kinesin family member 1B</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 2A1 [MIM:118210]
+Pheochromocytoma [MIM:171300]
+Neuroblastoma [MIM:256700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIF21A">
+ <field name="name">KIF21A</field>
+ <field name="long_name">kinesin family member 21A</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q12</field>
+ <field name="info">
+Fibrosis of extraocular muscles, congenital, 1 [MIM:135700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIF5A">
+ <field name="name">KIF5A</field>
+ <field name="long_name">kinesin family member 5A</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Spastic paraplegia 10 [MIM:604187]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIR2DL2">
+ <field name="name">KIR2DL2</field>
+ <field name="long_name">killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIR2DL4">
+ <field name="name">KIR2DL4</field>
+ <field name="long_name">killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 4</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIR3DL1">
+ <field name="name">KIR3DL1</field>
+ <field name="long_name">killer cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+AIDS, delayed/rapid progression to [MIM:609423]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIR3DS1">
+ <field name="name">KIR3DS1</field>
+ <field name="long_name">killer cell immunoglobulin-like receptor, three domains, short cytoplasmic tail, 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+AIDS, delayed/rapid progression to [MIM:609423]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIRREL3">
+ <field name="name">KIRREL3</field>
+ <field name="long_name">kin of IRRE like 3 (Drosophila)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q24.2</field>
+ <field name="info">
+Mental retardation, autosomal dominant 4 [MIM:612581]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KISS1R">
+ <field name="name">KISS1R</field>
+ <field name="long_name">KISS1 receptor</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Hypogonadotropic hypogonadism [MIM:146110]
+Precocious puberty, central [MIM:176400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KISS1">
+ <field name="name">KISS1</field>
+ <field name="long_name">KiSS-1 metastasis-suppressor</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KITLG">
+ <field name="name">KITLG</field>
+ <field name="long_name">KIT ligand</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q22</field>
+ <field name="info">
+Skin/hair/eye pigmentation 7, blond/brown hair [MIM:611664]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KIT">
+ <field name="name">KIT</field>
+ <field name="long_name">v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q12</field>
+ <field name="info">
+Piebaldism
+Mast cell leukemia
+Mastocytosis with associated hematologic disorder
+Germ cell tumors [MIM:273300]
+Gastrointestinal stromal tumor, somatic [MIM:606764]
+Leukemia, acute myeloid [MIM:601626]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KLF11">
+ <field name="name">KLF11</field>
+ <field name="long_name">Kruppel-like factor 11</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p25</field>
+ <field name="info">
+Maturity-onset diabetes of the young, type VII [MIM:610508]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KLF1">
+ <field name="name">KLF1</field>
+ <field name="long_name">Kruppel-like factor 1 (erythroid)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.13-p13.12</field>
+ <field name="info">
+Blood group--Lutheran inhibitor [MIM:111150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KLF6">
+ <field name="name">KLF6</field>
+ <field name="long_name">Kruppel-like factor 6</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p15</field>
+ <field name="info">
+Prostate cancer, somatic [MIM:176807]
+Gastric cancer, somatic [MIM:137215]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KLF7">
+ <field name="name">KLF7</field>
+ <field name="long_name">Kruppel-like factor 7 (ubiquitous)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KLK12">
+ <field name="name">KLK12</field>
+ <field name="long_name">kallikrein-related peptidase 12</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KLK1">
+ <field name="name">KLK1</field>
+ <field name="long_name">kallikrein 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+Kallikrein, decreased urinary activity of</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KLK3">
+ <field name="name">KLK3</field>
+ <field name="long_name">kallikrein-related peptidase 3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KLK4">
+ <field name="name">KLK4</field>
+ <field name="long_name">kallikrein-related peptidase 4</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+Amelogenesis imperfecta, pigmented hypomaturation type [MIM:204700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KLKB1">
+ <field name="name">KLKB1</field>
+ <field name="long_name">kallikrein B, plasma (Fletcher factor) 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q35</field>
+ <field name="info">
+Fletcher factor deficiency [MIM:612423]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KL">
+ <field name="name">KL</field>
+ <field name="long_name">klotho</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12</field>
+ <field name="info">
+Coronary artery disease, susceptibility to
+Tumoral calcinosis, hyperphosphatemic [MIM:211900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KMS">
+ <field name="name">KMS</field>
+ <field name="long_name">Kabuki mental retardation syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3</field>
+ <field name="info">
+Kallmann syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KNG1">
+ <field name="name">KNG1</field>
+ <field name="long_name">kininogen 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27</field>
+ <field name="info">
+Kininogen deficiency [MIM:228960]
+High molecular weight kininogen deficiency [MIM:228960]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KNO3">
+ <field name="name">KNO3</field>
+ <field name="long_name">Knoblocy syndrome, type III</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2</field>
+ <field name="info">
+Knobloch syndrome, type III</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRAS1P">
+ <field name="name">KRAS1P</field>
+ <field name="long_name">v-Ki-ras1 Kirsten rat sarcoma 1 viral oncogene homolog, processed pseudogene</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p12.1</field>
+ <field name="info">
+Lung cancer [MIM:211980]
+Bladder cancer [MIM:109800]
+Breast cancer, somatic [MIM:114480]
+Pancreatic carcinoma, somatic [MIM:260350]
+Stomach cancer [MIM:137215]
+Leukemia, acute myelogenous
+Noonan syndrome 3 [MIM:609942]
+Costello syndrome [MIM:218040]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRIT1">
+ <field name="name">KRIT1</field>
+ <field name="long_name">KRIT1, ankyrin repeat containing</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.2-q21</field>
+ <field name="info">
+Cerebral cavernous malformations-1 [MIM:116860]
+Hyperkeratotic cutaneous capillary-venous malformations associated with cerebral capillary malformations [MIM:116860]
+Cavernous malformations of CNS and retina [MIM:116860]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRIZI">
+ <field name="name">KRIZI</field>
+ <field name="long_name">Kahrizi syndrome</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p12-q12</field>
+ <field name="info">
+Kahrizi syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT10">
+ <field name="name">KRT10</field>
+ <field name="long_name">keratin 10</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+Epidermolytic hyperkeratosis [MIM:113800]
+Nevus, epidermal, epidermolytic hyperkeratotic type [MIM:600648]
+Ichthyosis, cyclic, with epidermolytic hyperkeratosis [MIM:607602]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT12">
+ <field name="name">KRT12</field>
+ <field name="long_name">keratin 12</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12</field>
+ <field name="info">
+Meesmann corneal dystrophy [MIM:122100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT13">
+ <field name="name">KRT13</field>
+ <field name="long_name">keratin 13</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+White sponge nevus [MIM:193900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT14">
+ <field name="name">KRT14</field>
+ <field name="long_name">keratin 14</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12-q21</field>
+ <field name="info">
+Epidermolysis bullosa simplex, Dowling-Meara type [MIM:131760]
+Epidermolysis bullosa simplex, Koebner type [MIM:131900]
+Epidermolysis bullosa simplex, recessive [MIM:601001]
+Naegeli-Franceschetti-Jadassohn syndrome [MIM:161000]
+Dermatopathia pigmentosa reticularis [MIM:125595]
+Epidermolysis bullosa simplex, Weber-Cockayne type [MIM:131800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT16">
+ <field name="name">KRT16</field>
+ <field name="long_name">keratin 16</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12-q21</field>
+ <field name="info">
+Pachyonychia congenita, Jadassohn-Lewandowsky type [MIM:167200]
+Palmoplantar keratoderma, nonepidermolytic [MIM:600962]
+Palmoplantar verrucous nevus, unilateral [MIM:144200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT17">
+ <field name="name">KRT17</field>
+ <field name="long_name">keratin 17</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12-q21</field>
+ <field name="info">
+Pachyonychia congenita, Jackson-Lawler type [MIM:167210]
+Steatocystoma multiplex [MIM:184500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT18">
+ <field name="name">KRT18</field>
+ <field name="long_name">keratin 18</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Cirrhosis, cryptogenic
+Cirrhosis, noncryptogenic, susceptibility to [MIM:215600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT1">
+ <field name="name">KRT1</field>
+ <field name="long_name">keratin 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Epidermolytic hyperkeratosis [MIM:113800]
+Cyclic ichthyosis with epidermolytic hyperkeratosis [MIM:607602]
+Keratosis palmoplantaria striata [MIM:148700]
+Ichthyosis histrix, Curth-Macklin type [MIM:146590]
+Unna-Thost disease, nonepidermolytic [MIM:600962]
+Keratosis palmoplantaris striata III [MIM:607654]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT2">
+ <field name="name">KRT2</field>
+ <field name="long_name">keratin 2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q11-q13</field>
+ <field name="info">
+Ichthyosis bullosa of Siemens [MIM:146800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT31">
+ <field name="name">KRT31</field>
+ <field name="long_name">keratin 31</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12-q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT3">
+ <field name="name">KRT3</field>
+ <field name="long_name">keratin 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Meesmann corneal dystrophy [MIM:122100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT4">
+ <field name="name">KRT4</field>
+ <field name="long_name">keratin 4</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+White sponge nevus [MIM:193900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT5">
+ <field name="name">KRT5</field>
+ <field name="long_name">keratin 5</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Epidermolysis bullosa simplex, Dowling-Meara type [MIM:131760]
+Epidermolysis bullosa simplex, Koebner type [MIM:131900]
+Epidermolysis bullosa simplex, Weber-Cockayne type [MIM:131800]
+Epidermolysis bullosa simplex with mottled pigmentation [MIM:131960]
+Dowling-Degos disease [MIM:179850]
+Epidermolysis bullosa simplex with migratory circinate erythema [MIM:609352]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT6A">
+ <field name="name">KRT6A</field>
+ <field name="long_name">keratin 6A</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Pachyonychia congenita, Jadassohn-Lewandowsky type [MIM:167200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT6B">
+ <field name="name">KRT6B</field>
+ <field name="long_name">keratin 6B</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Pachyonychia congenita, Jackson-Lawler type [MIM:167210]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT75">
+ <field name="name">KRT75</field>
+ <field name="long_name">keratin 75</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Pseudofolliculitis barbae, susceptibility to [MIM:612318]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT81">
+ <field name="name">KRT81</field>
+ <field name="long_name">keratin 81</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Monilethrix [MIM:158000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT83">
+ <field name="name">KRT83</field>
+ <field name="long_name">keratin 83</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Monilethrix [MIM:158000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT85">
+ <field name="name">KRT85</field>
+ <field name="long_name">keratin 85</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Ectodermal dysplasia, 'pure' hair-nail type [MIM:602032]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT86">
+ <field name="name">KRT86</field>
+ <field name="long_name">keratin 86</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Monilethrix [MIM:158000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT8">
+ <field name="name">KRT8</field>
+ <field name="long_name">keratin 8</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Cirrhosis, cryptogenic
+Cirrhosis, noncryptogenic, susceptibility to [MIM:215600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRT9">
+ <field name="name">KRT9</field>
+ <field name="long_name">keratin 9</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12-q21</field>
+ <field name="info">
+Epidermolytic palmoplantar keratoderma [MIM:144200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KRTAP1-1">
+ <field name="name">KRTAP1-1</field>
+ <field name="long_name">keratin associated protein 1-1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12-q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="KTCN2">
+ <field name="name">KTCN2</field>
+ <field name="long_name">Keratoconus 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22.3-q23.1</field>
+ <field name="info">
+Keratoconus 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KTCN3">
+ <field name="name">KTCN3</field>
+ <field name="long_name">Keratoconus 3</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p14-q13</field>
+ <field name="info">
+Keratoconus 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KTCN4">
+ <field name="name">KTCN4</field>
+ <field name="long_name">Keratoconus 4</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p24</field>
+ <field name="info">
+Keratoconus 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KTWS">
+ <field name="name">KTWS</field>
+ <field name="long_name">Klippel-Trenaunay-Weber syndrome</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q22.3</field>
+ <field name="info">
+Klippel-Trenaunay-Weber syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KWE">
+ <field name="name">KWE</field>
+ <field name="long_name">keratolytic winter erythema (Oudtshoorn skin disease)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23-p22</field>
+ <field name="info">
+Keratolytic winter erythema</field>
+</record>
+<record model="gnuhealth.disease.gene" id="KYPSC1">
+ <field name="name">KYPSC1</field>
+ <field name="long_name">Kyphoscoliosis 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13</field>
+ <field name="info">
+Kyphoscoliosis 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="L1CAM">
+ <field name="name">L1CAM</field>
+ <field name="long_name">L1 cell adhesion molecule</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Hydrocephalus due to aqueductal stenosis [MIM:307000]
+MASA syndrome [MIM:303350]
+CRASH syndrome [MIM:303350]
+Hydrocephalus with Hirschsprung disease and cleft palate [MIM:142623]
+Hydrocephalus with congenital idiopathic intestinal pseudoobstruction [MIM:307000]
+Corpus callosum, partial agenesis of [MIM:304100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="L2HGDH">
+ <field name="name">L2HGDH</field>
+ <field name="long_name">L-2-hydroxyglutarate dehydrogenase</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q22.1</field>
+ <field name="info">
+L-2-hydroxyglutaric aciduria [MIM:236792]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LAG5">
+ <field name="name">LAG5</field>
+ <field name="long_name">Leukocyte antigen group 5</field>
+ <field name="chromosome">4</field>
+ <field name="location">4</field>
+ <field name="info">
+Neutropenia, neonatal alloimmune</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LALL">
+ <field name="name">LALL</field>
+ <field name="long_name">Lymphomatous acute lymphoblastic leukemia</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p22-p21</field>
+ <field name="info">
+Leukemia, acute lymphoblastic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LAMA2">
+ <field name="name">LAMA2</field>
+ <field name="long_name">laminin, alpha 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q22-q23</field>
+ <field name="info">
+Muscular dystrophy, congenital merosin-deficient [MIM:607855]
+Muscular dystrophy, congenital, due to partial LAMA2 deficiency [MIM:607855]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LAMA3">
+ <field name="name">LAMA3</field>
+ <field name="long_name">laminin, alpha 3</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q11.2</field>
+ <field name="info">
+Epidermolysis bullosa, junctional, Herlitz type [MIM:226700]
+Epidermolysis bullosa, generalized atrophic benign [MIM:226650]
+Laryngoonychocutaneous syndrome [MIM:245660]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LAMA4">
+ <field name="name">LAMA4</field>
+ <field name="long_name">laminin, alpha 4</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LAMB1">
+ <field name="name">LAMB1</field>
+ <field name="long_name">laminin, beta 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31.1-q31.3</field>
+ <field name="info">
+Cutis laxa, marfanoid neonatal type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LAMB2">
+ <field name="name">LAMB2</field>
+ <field name="long_name">laminin, beta 2 (laminin S)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21</field>
+ <field name="info">
+Nephrosis, congenital, with or without ocular abnormalities [MIM:609049]
+Pierson syndrome [MIM:609049]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LAMB3">
+ <field name="name">LAMB3</field>
+ <field name="long_name">laminin, beta 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+Epidermolysis bullosa, junctional, Herlitz type [MIM:226700]
+Epidermolysis bullosa, junctional, non-Herlitz type [MIM:226650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LAMC1">
+ <field name="name">LAMC1</field>
+ <field name="long_name">laminin, gamma 1 (formerly LAMB2)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31</field>
+ <field name="info">
+Pelvic organ prolapse, susceptibility to [MIM:176780]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LAMC2">
+ <field name="name">LAMC2</field>
+ <field name="long_name">laminin, gamma 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q25-q31</field>
+ <field name="info">
+Epidermolysis bullosa, junctional, Herlitz type [MIM:226700]
+Epidermolysis bullosa, junctional, non-Herlitz type [MIM:226650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LAMP2">
+ <field name="name">LAMP2</field>
+ <field name="long_name">lysosomal-associated membrane protein 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24</field>
+ <field name="info">
+Glycogen storage disease IIb [MIM:300257]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LAP">
+ <field name="name">LAP</field>
+ <field name="long_name">Laryngeal adductor paralysis</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3-p21.2</field>
+ <field name="info">
+Laryngeal adductor paralysis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LARGE">
+ <field name="name">LARGE</field>
+ <field name="long_name">like-glycosyltransferase</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.3-q13.1</field>
+ <field name="info">
+Muscular dystrophy, congenital, type 1D [MIM:608840]
+Walker-Warburg syndrome [MIM:236670]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LARS2">
+ <field name="name">LARS2</field>
+ <field name="long_name">leucyl-tRNA synthetase 2, mitochondrial</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LAT">
+ <field name="name">LAT</field>
+ <field name="long_name">linker for activation of T cells</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LBMQTL1">
+ <field name="name">LBMQTL1</field>
+ <field name="long_name">Lean body mass QTL 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q23</field>
+ <field name="info">
+Lean body mass QTL 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LBR">
+ <field name="name">LBR</field>
+ <field name="long_name">lamin B receptor</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42.1</field>
+ <field name="info">
+Pelger-Huet anomaly [MIM:169400]
+Greenberg dysplasia [MIM:215140]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LCA3">
+ <field name="name">LCA3</field>
+ <field name="long_name">Leber congenital amaurosis 3</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q31.3</field>
+ <field name="info">
+Leber congenital amaurosis 3 [MIM:604232]
+Retinitis pigmentosa, juvenile, autosomal recessive [MIM:268000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LCA5">
+ <field name="name">LCA5</field>
+ <field name="long_name">Leber congenital amaurosis 5</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q14.1</field>
+ <field name="info">
+Leber congenital amaurosis 5 [MIM:604537]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LCA9">
+ <field name="name">LCA9</field>
+ <field name="long_name">Leber congenital amaurosis 9</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Leber congenital amaurosis 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LCAT">
+ <field name="name">LCAT</field>
+ <field name="long_name">lecithin-cholesterol acyltransferase</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22.1</field>
+ <field name="info">
+Norum disease [MIM:245900]
+Fish-eye disease [MIM:136120]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LCE5A">
+ <field name="name">LCE5A</field>
+ <field name="long_name">late cornified envelope 5A</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LCK">
+ <field name="name">LCK</field>
+ <field name="long_name">lymphocyte-specific protein tyrosine kinase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p35-p34.3</field>
+ <field name="info">
+SCID due to LCK deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LCO">
+ <field name="name">LCO</field>
+ <field name="long_name">liver cancer oncogene</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14-q21</field>
+ <field name="info">
+Hepatocellular carcinoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LCRB">
+ <field name="name">LCRB</field>
+ <field name="long_name">locus control region, beta</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Thalassemia, Hispanic gamma-delta-beta [MIM:604131]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LCS1">
+ <field name="name">LCS1</field>
+ <field name="long_name">lymphedema-cholestasis syndrome 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q</field>
+ <field name="info">
+Cholestasis-lymphedema syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LCT">
+ <field name="name">LCT</field>
+ <field name="long_name">lactase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q21</field>
+ <field name="info">
+Lactase deficiency, congenital [MIM:223000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LDB3">
+ <field name="name">LDB3</field>
+ <field name="long_name">LIM domain binding 3</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.2-q23.3</field>
+ <field name="info">
+Myopathy, myofibrillar, ZASP-related [MIM:609452]
+Cardiomyopathy, dilated
+Cardiomyopathy, dilated, with left ventricular noncompaction</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LDHA">
+ <field name="name">LDHA</field>
+ <field name="long_name">lactate dehydrogenase A</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.4</field>
+ <field name="info">
+Exertional myoglobinuria due to deficiency of LDH-A</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LDHB">
+ <field name="name">LDHB</field>
+ <field name="long_name">lactate dehydrogenase B</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p12.2-p12.1</field>
+ <field name="info">
+Lactate dehydrogenase-B deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LDLRAP1">
+ <field name="name">LDLRAP1</field>
+ <field name="long_name">low density lipoprotein receptor adaptor protein 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36-p35</field>
+ <field name="info">
+Hypercholesterolemia, familial, autosomal recessive [MIM:603813]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LDLR">
+ <field name="name">LDLR</field>
+ <field name="long_name">low density lipoprotein receptor</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2</field>
+ <field name="info">
+Hypercholesterolemia, familial [MIM:143890]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LEF1">
+ <field name="name">LEF1</field>
+ <field name="long_name">lymphoid enhancer-binding factor 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q23-q25</field>
+ <field name="info">
+Sebaceous tumors, somatic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LEFTY2">
+ <field name="name">LEFTY2</field>
+ <field name="long_name">left-right determination factor 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42.1</field>
+ <field name="info">
+Left-right axis malformations</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LEMD3">
+ <field name="name">LEMD3</field>
+ <field name="long_name">LEM domain containing 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q14</field>
+ <field name="info">
+Osteopoikilosis [MIM:166700]
+Buschke-Ollendorff syndrome [MIM:166700]
+Melorheostosis with osteopoikilosis [MIM:155950]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LEPRE1">
+ <field name="name">LEPRE1</field>
+ <field name="long_name">leucine proline-enriched proteoglycan (leprecan) 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34</field>
+ <field name="info">
+Osteogenesis imperfecta, type VIII [MIM:610915]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LEPR">
+ <field name="name">LEPR</field>
+ <field name="long_name">leptin receptor</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+Obesity, morbid, with hypogonadism</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LEP">
+ <field name="name">LEP</field>
+ <field name="long_name">leptin</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31.3</field>
+ <field name="info">
+Obesity, severe, due to leptin deficiency
+Obesity, morbid, with hypogonadism</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LFNG">
+ <field name="name">LFNG</field>
+ <field name="long_name">LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p22</field>
+ <field name="info">
+Spondylocostal dysostosis, autosomal recessive 3 [MIM:609813]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LFS3">
+ <field name="name">LFS3</field>
+ <field name="long_name">Li-Fraumeni syndrome 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23</field>
+ <field name="info">
+Li-Fraumeni syndrome 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LGALS2">
+ <field name="name">LGALS2</field>
+ <field name="long_name">lectin, galactoside-binding, soluble, 2</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.1</field>
+ <field name="info">
+Myocardial infarction, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LGALS3">
+ <field name="name">LGALS3</field>
+ <field name="long_name">lectin, galactoside-binding, soluble, 3</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q21-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LGI1">
+ <field name="name">LGI1</field>
+ <field name="long_name">leucine-rich, glioma inactivated 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+Epilepsy, partial, with auditory features [MIM:600512]
+Glioblastoma, somatic [MIM:137800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LGMBF">
+ <field name="name">LGMBF</field>
+ <field name="long_name">myopathy, limb-girdle, with bone fragility</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p22-p21</field>
+ <field name="info">
+Myopathy, limb-girdle, with bone fragility</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LGMD1D">
+ <field name="name">LGMD1D</field>
+ <field name="long_name">limb girdle muscular dystrophy 1D (autosomal dominant)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q</field>
+ <field name="info">
+Muscular dystrophy, limb-girdle, type 1D</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LGMD1F">
+ <field name="name">LGMD1F</field>
+ <field name="long_name">limb girdle muscular dystrophy 1F (autosomal dominant)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q32.1-q32.2</field>
+ <field name="info">
+Muscular dystrophy, limb-girdle, type 1F</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LGMD1G">
+ <field name="name">LGMD1G</field>
+ <field name="long_name">limb girdle muscular dystrophy 1G (autosomal dominant)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21</field>
+ <field name="info">
+Limb-girdle muscular dystrophy, type 1G</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LGMD2L">
+ <field name="name">LGMD2L</field>
+ <field name="long_name">limb girdle muscular dystrophy 2L (autosomal recessive)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13-p12</field>
+ <field name="info">
+Muscular dystrophy, limb-girdle, type 2L</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LGV1">
+ <field name="name">LGV1</field>
+ <field name="long_name">Longevity 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q25</field>
+ <field name="info">
+Longevity [MIM:152430]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LHB">
+ <field name="name">LHB</field>
+ <field name="long_name">luteinizing hormone beta polypeptide</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.32</field>
+ <field name="info">
+Hypogonadism, hypergonadotropic
+Male pseudohermaphroditism due to defective LH</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LHCGR">
+ <field name="name">LHCGR</field>
+ <field name="long_name">luteinizing hormone/choriogonadotropin receptor</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p21</field>
+ <field name="info">
+Precocious puberty, male [MIM:176410]
+Leydig cell hypoplasia with pseudohermaphroditism [MIM:238320]
+Leydig cell hypoplasia with hypergonadotropic hypogonadism [MIM:238320]
+Luteinizing hormone resistance, female [MIM:238320]
+Leydig cell adenoma, somatic, with precocious puberty [MIM:176410]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LHFPL5">
+ <field name="name">LHFPL5</field>
+ <field name="long_name">lipoma HMGIC fusion partner-like 5</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Deafness, autosomal recessive 67 [MIM:610265]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LHX3">
+ <field name="name">LHX3</field>
+ <field name="long_name">LIM homeobox 3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.3</field>
+ <field name="info">
+Pituitary hormone deficiency, combined, with rigid cervical spine [MIM:262600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LHX4">
+ <field name="name">LHX4</field>
+ <field name="long_name">LIM homeobox 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q25</field>
+ <field name="info">
+Short stature, pituitary and cerebellar defects, and small sella turcica [MIM:606606]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LHX8">
+ <field name="name">LHX8</field>
+ <field name="long_name">LIM homeobox 8</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LI5">
+ <field name="name">LI5</field>
+ <field name="long_name">Lamellar ichthyosis 5</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.2-p13.1</field>
+ <field name="info">
+Ichthyosis, lamellar, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LIFR">
+ <field name="name">LIFR</field>
+ <field name="long_name">leukemia inhibitory factor receptor alpha</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13.1</field>
+ <field name="info">
+Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome [MIM:601559]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LIF">
+ <field name="name">LIF</field>
+ <field name="long_name">leukemia inhibitory factor (cholinergic differentiation factor)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.1-q12.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LIG1">
+ <field name="name">LIG1</field>
+ <field name="long_name">ligase I, DNA, ATP-dependent</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2-q13.3</field>
+ <field name="info">
+DNA ligase I deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LIG3">
+ <field name="name">LIG3</field>
+ <field name="long_name">ligase III, DNA, ATP-dependent</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2-q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LIG4">
+ <field name="name">LIG4</field>
+ <field name="long_name">ligase IV, DNA, ATP-dependent</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q22-q34</field>
+ <field name="info">
+LIG4 syndrome [MIM:606593]
+Multiple myeloma, resistance to [MIM:254500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LILRA3">
+ <field name="name">LILRA3</field>
+ <field name="long_name">leukocyte immunoglobulin-like receptor, subfamily A (without TM domain), member 3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LIM2">
+ <field name="name">LIM2</field>
+ <field name="long_name">lens intrinsic membrane protein 2, 19kDa</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+Cataract, cortical pulverulent, late-onset</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LIPA">
+ <field name="name">LIPA</field>
+ <field name="long_name">lipase A, lysosomal acid, cholesterol esterase</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24-q25</field>
+ <field name="info">
+Wolman disease
+Cholesteryl ester storage disease</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LIPC">
+ <field name="name">LIPC</field>
+ <field name="long_name">lipase, hepatic</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21-q23</field>
+ <field name="info">
+Hepatic lipase deficiency
+High density lipoprotein cholesterol level QTL 12
+Diabetes mellitus, noninsulin-dependent [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LIPE">
+ <field name="name">LIPE</field>
+ <field name="long_name">lipase, hormone-sensitive</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1-q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LIPG">
+ <field name="name">LIPG</field>
+ <field name="long_name">lipase, endothelial</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LIPH">
+ <field name="name">LIPH</field>
+ <field name="long_name">lipase, member H</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27-q28</field>
+ <field name="info">
+Hypotrichosis, total, Mari type [MIM:604379]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LIPI">
+ <field name="name">LIPI</field>
+ <field name="long_name">lipase, member I</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q11.2</field>
+ <field name="info">
+Hypertriglyceridemia, susceptibility to [MIM:145750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LITAF">
+ <field name="name">LITAF</field>
+ <field name="long_name">lipopolysaccharide-induced TNF factor</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3-p12</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 1C [MIM:601098]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LMAN1">
+ <field name="name">LMAN1</field>
+ <field name="long_name">lectin, mannose-binding, 1</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.3-q22</field>
+ <field name="info">
+Combined factor V and VIII deficiency [MIM:227300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LMBR1">
+ <field name="name">LMBR1</field>
+ <field name="long_name">limb region 1 homolog (mouse)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q36</field>
+ <field name="info">
+Acheiropody [MIM:200500]
+Polydactyly, preaxial type II [MIM:174500]
+Triphalangeal thumb, type I [MIM:174500]
+Triphalangeal thumb-polysyndactyly syndrome [MIM:174500]
+Syndactyly, type IV [MIM:186200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LMBRD1">
+ <field name="name">LMBRD1</field>
+ <field name="long_name">LMBR1 domain containing 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q13</field>
+ <field name="info">
+Methylmalonic aciduria and homocystinuria, cblF type [MIM:277380]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LMF1">
+ <field name="name">LMF1</field>
+ <field name="long_name">lipase maturation factor 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+Lipase deficiency, combined [MIM:246650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LMNA">
+ <field name="name">LMNA</field>
+ <field name="long_name">lamin A/C</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21.2</field>
+ <field name="info">
+Emery-Dreifuss muscular dystrophy, AD [MIM:181350]
+Cardiomyopathy, dilated, 1A [MIM:115200]
+Lipodystrophy, familial partial [MIM:151660]
+Emery-Dreifuss muscular dystrophy, AR [MIM:604929]
+Charcot-Marie-Tooth disease, type 2B1 [MIM:605588]
+Muscular dystrophy, limb-girdle, type 1B [MIM:159001]
+Mandibuloacral dysplasia [MIM:248370]
+Hutchinson-Gilford progeria [MIM:176670]
+LDHCP syndrome [MIM:608056]
+Werner syndrome, atypical [MIM:277700]
+Myopathy, early-onset, and progeroid features [MIM:176670]
+Restrictive dermopathy, lethal [MIM:275210]
+Arthropathy, tendinous calcinosis, and progeroid features [MIM:611618]
+Heart-hand syndrome, Slovenian type [MIM:610140]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LMNB1">
+ <field name="name">LMNB1</field>
+ <field name="long_name">lamin B1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q23.3-q31.1</field>
+ <field name="info">
+Leukodystrophy, adult-onset, autosomal dominant [MIM:169500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LMNB2">
+ <field name="name">LMNB2</field>
+ <field name="long_name">lamin B2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Lipodystrophy, partial, acquired [MIM:608709]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LMO1">
+ <field name="name">LMO1</field>
+ <field name="long_name">LIM domain only 1 (rhombotin 1)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15</field>
+ <field name="info">
+Leukemia, T-cell acute lymphoblastic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LMO2">
+ <field name="name">LMO2</field>
+ <field name="long_name">LIM domain only 2 (rhombotin-like 1)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13</field>
+ <field name="info">
+Leukemia, acute T-cell</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LMPH1B">
+ <field name="name">LMPH1B</field>
+ <field name="long_name">Lymphedema, hereditary, IB</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q16.2-q22.1</field>
+ <field name="info">
+Lymphedema, hereditary, IB</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LMX1B">
+ <field name="name">LMX1B</field>
+ <field name="long_name">LIM homeobox transcription factor 1, beta</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.1</field>
+ <field name="info">
+Nail-patella syndrome [MIM:161200]
+Nail-patella syndrome with open-angle glaucoma [MIM:137750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LNCR1">
+ <field name="name">LNCR1</field>
+ <field name="long_name">Lung cancer 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23-q25</field>
+ <field name="info">
+Lung cancer susceptibility</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LNCR3">
+ <field name="name">LNCR3</field>
+ <field name="long_name">Lung cancer susceptibility 3</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.33</field>
+ <field name="info">
+Lung cancer susceptibility 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LNCR4">
+ <field name="name">LNCR4</field>
+ <field name="long_name">Lung cancer susceptibility 4</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.33</field>
+ <field name="info">
+Lung cancer susceptibility 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LOAS">
+ <field name="name">LOAS</field>
+ <field name="long_name">Leber optic atrophy, susceptibility to</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11</field>
+ <field name="info">
+Leber optic atrophy, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LOC344967">
+ <field name="name">LOC344967</field>
+ <field name="long_name">acyl-CoA thioesterase 7 pseudogene</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p14-p11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LOR">
+ <field name="name">LOR</field>
+ <field name="long_name">loricrin</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Vohwinkel syndrome with ichthyosis [MIM:604117]
+Erythrokeratoderma, progressive symmetric [MIM:602036]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LOXL1">
+ <field name="name">LOXL1</field>
+ <field name="long_name">lysyl oxidase-like 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22</field>
+ <field name="info">
+Exfoliation syndrome, susceptibility to [MIM:177650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LOXL2">
+ <field name="name">LOXL2</field>
+ <field name="long_name">lysyl oxidase-like 2</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21.3-p21.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LOX">
+ <field name="name">LOX</field>
+ <field name="long_name">lysyl oxidase</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q23.3-q31.2</field>
+ <field name="info">
+Cutis laxa, recessive, type I [MIM:219100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LPAR1">
+ <field name="name">LPAR1</field>
+ <field name="long_name">lysophosphatidic acid receptor 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q31.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LPA">
+ <field name="name">LPA</field>
+ <field name="long_name">lipoprotein, Lp(a)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q27</field>
+ <field name="info">
+Coronary artery disease, susceptibility to
+LPA deficiency, congenital</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LPIN1">
+ <field name="name">LPIN1</field>
+ <field name="long_name">lipin 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p21</field>
+ <field name="info">
+Myoglobinuria, acute recurrent, autosomal recessive [MIM:268200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LPIN2">
+ <field name="name">LPIN2</field>
+ <field name="long_name">lipin 2</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p</field>
+ <field name="info">
+Majeed syndrome [MIM:609628]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LPL">
+ <field name="name">LPL</field>
+ <field name="long_name">lipoprotein lipase</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p22</field>
+ <field name="info">
+Lipoprotein lipase deficiency [MIM:238600]
+Combined hyperlipidemia, familial [MIM:144250]
+High density lipoprotein cholesterol level QTL 11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LPP">
+ <field name="name">LPP</field>
+ <field name="long_name">LIM domain containing preferred translocation partner in lipoma</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q28</field>
+ <field name="info">
+Lipoma
+Leukemia, acute myeloid [MIM:601626]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LPSA">
+ <field name="name">LPSA</field>
+ <field name="long_name">Oncogene liposarcoma (DNA segment, single copy, expressed, probes</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2-q13.3</field>
+ <field name="info">
+Liposarcoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LRAT">
+ <field name="name">LRAT</field>
+ <field name="long_name">lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q31</field>
+ <field name="info">
+Retinal dystrophy, early-onset severe</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LRCH1">
+ <field name="name">LRCH1</field>
+ <field name="long_name">leucine-rich repeats and calponin homology (CH) domain containing 1</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LRP1">
+ <field name="name">LRP1</field>
+ <field name="long_name">low density lipoprotein-related protein 1 (alpha-2-macroglobulin receptor)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13.1-q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LRP2">
+ <field name="name">LRP2</field>
+ <field name="long_name">low density lipoprotein-related protein 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q24-q31</field>
+ <field name="info">
+Donnai-Barrow syndrome [MIM:222448]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LRP5">
+ <field name="name">LRP5</field>
+ <field name="long_name">low density lipoprotein receptor-related protein 5</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.4</field>
+ <field name="info">
+Osteoporosis-pseudoglioma syndrome [MIM:259770]
+Bone mineral density variability 1 [MIM:601884]
+Osteopetrosis, AD type I [MIM:607634]
+Hyperostosis, endosteal [MIM:144750]
+van Buchem disease, type 2 [MIM:607636]
+Osteosclerosis [MIM:144750]
+Osteoporosis [MIM:166710]
+Exudative vitreoretinopathy 4 [MIM:601813]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LRP6">
+ <field name="name">LRP6</field>
+ <field name="long_name">low density lipoprotein receptor-related protein 6</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.3-p11.2</field>
+ <field name="info">
+Coronary artery disease, autosomal dominant, 2 [MIM:610947]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LRP8">
+ <field name="name">LRP8</field>
+ <field name="long_name">low density lipoprotein receptor-related protein 8, apolipoprotein e receptor</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34</field>
+ <field name="info">
+Myocardial infarction, susceptibility to [MIM:608446]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LRPAP1">
+ <field name="name">LRPAP1</field>
+ <field name="long_name">low density lipoprotein receptor-related protein associated protein 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LRPPRC">
+ <field name="name">LRPPRC</field>
+ <field name="long_name">leucine-rich PPR-motif containing</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p21-p16</field>
+ <field name="info">
+Leigh syndrome, French-Canadian type [MIM:220111]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LRRK2">
+ <field name="name">LRRK2</field>
+ <field name="long_name">leucine-rich repeat kinase 2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q12</field>
+ <field name="info">
+Parkinson disease-8 [MIM:607060]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LRS1">
+ <field name="name">LRS1</field>
+ <field name="long_name">Larsen syndrome 1 (autosomal dominant)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p14.3</field>
+ <field name="info">
+Spondylocarpotarsal synostosis syndrome [MIM:272460]
+Larsen syndrome [MIM:150250]
+Atelostogenesis, type I [MIM:108720]
+Atelosteogenesis, type III [MIM:108721]
+Boomerang dysplasia [MIM:112310]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LRSL">
+ <field name="name">LRSL</field>
+ <field name="long_name">Larsen-like syndrome</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p25</field>
+ <field name="info">
+Larsen-like syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LRTOMT">
+ <field name="name">LRTOMT</field>
+ <field name="long_name">leucine rich transmembrane and 0-methyltransferase domain containing</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.3-q13.4</field>
+ <field name="info">
+Deafness, autosomal recessive 63 [MIM:611451]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LSL">
+ <field name="name">LSL</field>
+ <field name="long_name">Leptin, serum levels of</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p21</field>
+ <field name="info">
+Myoglobinuria, acute recurrent, autosomal recessive [MIM:268200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LTA">
+ <field name="name">LTA</field>
+ <field name="long_name">lymphotoxin alpha (TNF superfamily, member 1)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Myocardial infarction, susceptibility to
+Psoriatic arthritis, susceptibility to [MIM:607507]
+Leprosy, susceptibility to, 4 [MIM:610988]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LTBP1">
+ <field name="name">LTBP1</field>
+ <field name="long_name">latent transforming growth factor beta binding protein 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p12-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LTBP2">
+ <field name="name">LTBP2</field>
+ <field name="long_name">latent transforming growth factor beta binding protein 2</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LTC4S">
+ <field name="name">LTC4S</field>
+ <field name="long_name">leukotriene C4 synthase</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q35</field>
+ <field name="info">
+Leukotriene C4 synthase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LTF">
+ <field name="name">LTF</field>
+ <field name="long_name">lactotransferrin</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LTK">
+ <field name="name">LTK</field>
+ <field name="long_name">leukocyte receptor tyrosine kinase</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15.1-q21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LVNC2">
+ <field name="name">LVNC2</field>
+ <field name="long_name">noncompaction of left ventricular myocardium, familial isolated, autosomal dominant 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15</field>
+ <field name="info">
+Noncompaction of left ventricular myocardium, familial isolated, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LYL1">
+ <field name="name">LYL1</field>
+ <field name="long_name">lymphoblastic leukemia derived sequence 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2-p13.1</field>
+ <field name="info">
+Leukemia, T-cell acute lymphoblastoid</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LYN">
+ <field name="name">LYN</field>
+ <field name="long_name">v-yes-1 Yamaguchi sarcoma viral related oncogene homolog</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q13-qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="LYST">
+ <field name="name">LYST</field>
+ <field name="long_name">lysosomal trafficking regulator</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42.1-q42.2</field>
+ <field name="info">
+Chediak-Higashi syndrome [MIM:214500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LYZ">
+ <field name="name">LYZ</field>
+ <field name="long_name">lysozyme (renal amyloidosis)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q15</field>
+ <field name="info">
+Amyloidosis, renal [MIM:105200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="LZTS1">
+ <field name="name">LZTS1</field>
+ <field name="long_name">leucine zipper, putative tumor suppressor 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p22</field>
+ <field name="info">
+Esophageal squamous cell carcinoma [MIM:133239]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAA">
+ <field name="name">MAA</field>
+ <field name="long_name">microphthalmia or anophthalmia and associated anomalies</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq27-q28</field>
+ <field name="info">
+Microphthalmia, syndromic 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MACROD2">
+ <field name="name">MACROD2</field>
+ <field name="long_name">MACRO domain containing 2</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAD1L1">
+ <field name="name">MAD1L1</field>
+ <field name="long_name">MAD1 mitotic arrest deficient-like 1 (yeast)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p22</field>
+ <field name="info">
+Lymphoma, somatic
+Prostate cancer, somatic [MIM:176807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAFD1">
+ <field name="name">MAFD1</field>
+ <field name="long_name">major affective disorder 1</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p</field>
+ <field name="info">
+Major affective disorder 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAFD2">
+ <field name="name">MAFD2</field>
+ <field name="long_name">major affective disorder 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Major affective disorder 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAFD3">
+ <field name="name">MAFD3</field>
+ <field name="long_name">Major affective disorder 3, early onset</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.13</field>
+ <field name="info">
+Major affective disorder 3, early onset</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAFD4">
+ <field name="name">MAFD4</field>
+ <field name="long_name">Major affective disorder 4</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12</field>
+ <field name="info">
+Major affective disorder 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAFD5">
+ <field name="name">MAFD5</field>
+ <field name="long_name">Major affective disorder 5</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q22-q24</field>
+ <field name="info">
+Major affective disorder 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAFD6">
+ <field name="name">MAFD6</field>
+ <field name="long_name">Major affective disorder 6</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23-q24</field>
+ <field name="info">
+Major affective disorder 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAFD8">
+ <field name="name">MAFD8</field>
+ <field name="long_name">Major affective disorder-8, susceptibility to</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21</field>
+ <field name="info">
+Major affective disorder-8, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAFD9">
+ <field name="name">MAFD9</field>
+ <field name="long_name">Major affective disorder-9, susceptibility to</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.3</field>
+ <field name="info">
+Major affective disorder-9, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAF">
+ <field name="name">MAF</field>
+ <field name="long_name">v-maf musculoaponeurotic fibrosarcoma oncogene homolog (avian)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22-q23</field>
+ <field name="info">
+Cataract, pulverulent, juvenile-onset [MIM:610202]
+Cataract, congenital, cerulean type, 4 [MIM:610202]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAGEE2">
+ <field name="name">MAGEE2</field>
+ <field name="long_name">melanoma antigen family E, 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAGT1">
+ <field name="name">MAGT1</field>
+ <field name="long_name">magnesium transporter 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.1-q13.2</field>
+ <field name="info">
+Mental retardation, X-linked 95 [MIM:300716]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAG">
+ <field name="name">MAG</field>
+ <field name="long_name">myelin associated glycoprotein</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MALL">
+ <field name="name">MALL</field>
+ <field name="long_name">mal, T-cell differentiation protein-like</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MALT1">
+ <field name="name">MALT1</field>
+ <field name="long_name">mucosa associated lymphoid tissue lymphoma translocation gene 1</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21</field>
+ <field name="info">
+MALT lymphoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAL">
+ <field name="name">MAL</field>
+ <field name="long_name">mal, T-cell differentiation protein</field>
+ <field name="chromosome">2</field>
+ <field name="location">2cen-q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAML2">
+ <field name="name">MAML2</field>
+ <field name="long_name">mastermind-like 2 (Drosophila)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q21</field>
+ <field name="info">
+Mucoepidermoid salivary gland carcinoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAMLD1">
+ <field name="name">MAMLD1</field>
+ <field name="long_name">mastermind-like domain containing 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Hypospadias 2, X-linked [MIM:300758]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAN1A2">
+ <field name="name">MAN1A2</field>
+ <field name="long_name">mannosidase, alpha, class 1A, member 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAN2B1">
+ <field name="name">MAN2B1</field>
+ <field name="long_name">mannosidase, alpha, class 2B, member 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19cen-q12</field>
+ <field name="info">
+Mannosidosis, alpha-, types I and II [MIM:248500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MANBA">
+ <field name="name">MANBA</field>
+ <field name="long_name">mannosidase, beta A, lysosomal</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q22-q25</field>
+ <field name="info">
+Mannosidosis, beta [MIM:248510]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAOA">
+ <field name="name">MAOA</field>
+ <field name="long_name">monoamine oxidase A</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23</field>
+ <field name="info">
+Brunner syndrome [MIM:300615]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAOB">
+ <field name="name">MAOB</field>
+ <field name="long_name">monoamine oxidase B</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23</field>
+ <field name="info">
+monoamine oxidase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAP2K1">
+ <field name="name">MAP2K1</field>
+ <field name="long_name">mitogen-activated protein kinase kinase 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21</field>
+ <field name="info">
+Cardiofaciocutaneous Syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAP2K2">
+ <field name="name">MAP2K2</field>
+ <field name="long_name">mitogen-activated protein kinase kinase 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q32</field>
+ <field name="info">
+Cardiofaciocutaneous Syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAP3K8">
+ <field name="name">MAP3K8</field>
+ <field name="long_name">mitogen-activated protein kinase kinase kinase 8</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p11.2</field>
+ <field name="info">
+Lung cancer, somatic [MIM:211980]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAP4K5">
+ <field name="name">MAP4K5</field>
+ <field name="long_name">mitogen-activated protein kinase kinase kinase kinase 5</field>
+ <field name="chromosome">14</field>
+ <field name="location">14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAPK10">
+ <field name="name">MAPK10</field>
+ <field name="long_name">mitogen-activated protein kinase 10</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21.3</field>
+ <field name="info">
+Epileptic encephalopathy, Lennox-Gastaut type [MIM:606369]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAPK8IP1">
+ <field name="name">MAPK8IP1</field>
+ <field name="long_name">mitogen-activated protein kinase 8 interacting protein 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p12-p11.2</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAPT">
+ <field name="name">MAPT</field>
+ <field name="long_name">microtubule-associated protein tau</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.1</field>
+ <field name="info">
+Dementia, frontotemporal, with or without parkinsonism [MIM:600274]
+Pick disease [MIM:172700]
+Supranuclear palsy, progressive [MIM:601104]
+Supranuclear palsy, progressive atypical [MIM:260540]
+Parkinson disease [MIM:168600]
+Tauopathy and respiratory failure</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MARVELD2">
+ <field name="name">MARVELD2</field>
+ <field name="long_name">MARVEL domain containing 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13.1</field>
+ <field name="info">
+Deafness, autosomal recessive 49 [MIM:610153]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MASP2">
+ <field name="name">MASP2</field>
+ <field name="long_name">mannan-binding lectin serine peptidase 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3-p36.2</field>
+ <field name="info">
+MASP2 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MAT1A">
+ <field name="name">MAT1A</field>
+ <field name="long_name">methionine adenosyltransferase I, alpha</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22</field>
+ <field name="info">
+Hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency [MIM:250850]
+Methionine adenosyltransferase deficiency, autosomal recessive [MIM:250850]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MATN3">
+ <field name="name">MATN3</field>
+ <field name="long_name">matrilin 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p24-p23</field>
+ <field name="info">
+Epiphyseal dysplasia, multiple, 5 [MIM:607078]
+Osteoarthritis susceptibility 2 [MIM:140600]
+Spondyloepimetaphyseal dysplasia [MIM:608728]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MA">
+ <field name="name">MA</field>
+ <field name="long_name">Migraine with aura, susceptibility to</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q24</field>
+ <field name="info">
+Migraine with or without aura, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MBD1">
+ <field name="name">MBD1</field>
+ <field name="long_name">methyl-CpG binding domain protein 1</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MBD4">
+ <field name="name">MBD4</field>
+ <field name="long_name">methyl-CpG binding domain protein 4</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MBD5">
+ <field name="name">MBD5</field>
+ <field name="long_name">methyl-CpG binding domain protein 5</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q23.1</field>
+ <field name="info">
+Mental retardation, autosomal dominant 1 [MIM:156200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MBL2">
+ <field name="name">MBL2</field>
+ <field name="long_name">mannose-binding lectin (protein C) 2, soluble (opsonic defect)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q11.2-q21</field>
+ <field name="info">
+Mannose-binding protein deficiency
+Diabetes mellitus, gestational, susceptibility to
+Meningococcal disease, susceptibility to
+Chronic infections, due to MBL deficiency
+Preterm delivery, susceptibility to (3) 14</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MBS1">
+ <field name="name">MBS1</field>
+ <field name="long_name">Moebius syndrome 1</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12.2-q13</field>
+ <field name="info">
+Moebius syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MBS2">
+ <field name="name">MBS2</field>
+ <field name="long_name">Moebius syndrome 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21-q22</field>
+ <field name="info">
+Facial paresis, hereditary congenital, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MBS3">
+ <field name="name">MBS3</field>
+ <field name="long_name">Moebius syndrome 3</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21.3-q22.1</field>
+ <field name="info">
+Moebius syndrome-3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MB">
+ <field name="name">MB</field>
+ <field name="long_name">myoglobin</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2-q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MC1R">
+ <field name="name">MC1R</field>
+ <field name="long_name">melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.3</field>
+ <field name="info">
+Skin/hair/eye pigmentation 2, red hair/fair skin [MIM:226300]
+Skin/hair/eye pigmentation 2, blond hair/fair skin [MIM:226300]
+Melanoma susceptibility to [MIM:155600]
+Analgesia from kappa-opioid receptor agonist, female-specific
+Oculocutaneous albinism, type II, modifier of [MIM:203200]
+UV-induced skin damage [MIM:266300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MC2R">
+ <field name="name">MC2R</field>
+ <field name="long_name">melanocortin 2 receptor (adrenocorticotropic hormone)</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.2</field>
+ <field name="info">
+Glucocorticoid deficiency, due to ACTH unresponsiveness [MIM:202200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MC3R">
+ <field name="name">MC3R</field>
+ <field name="long_name">melanocortin 3 receptor</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.2</field>
+ <field name="info">
+Obesity, severe, susceptibility to, BMIQ9 [MIM:602025]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MC4R">
+ <field name="name">MC4R</field>
+ <field name="long_name">melanocortin 4 receptor</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q22</field>
+ <field name="info">
+Obesity, autosomal dominant [MIM:601665]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCCC1">
+ <field name="name">MCCC1</field>
+ <field name="long_name">methylcrotonoyl-Coenzyme A carboxylase 1 (alpha)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q25-q27</field>
+ <field name="info">
+3-Methylcrotonyl-CoA carboxylase 1 deficiency [MIM:210200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCCC2">
+ <field name="name">MCCC2</field>
+ <field name="long_name">methylcrotonoyl-Coenzyme A carboxylase 2 (beta)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q12-q13</field>
+ <field name="info">
+3-Methylcrotonyl-CoA carboxylase 2 deficiency [MIM:210210]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCC">
+ <field name="name">MCC</field>
+ <field name="long_name">mutated in colorectal cancers</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q21</field>
+ <field name="info">
+Colorectal cancer</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCDR1">
+ <field name="name">MCDR1</field>
+ <field name="long_name">macular dystrophy, retinal, 1 (North Carolina type)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q14-q16.2</field>
+ <field name="info">
+Macular dystrophy, North Carolina type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCDR3">
+ <field name="name">MCDR3</field>
+ <field name="long_name">macular dystrophy, retinal 3</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.33-p13.1</field>
+ <field name="info">
+Macular dystrophy, retinal, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCEE">
+ <field name="name">MCEE</field>
+ <field name="long_name">methylmalonyl CoA epimerase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p13.3</field>
+ <field name="info">
+Methylmalonyl-CoA epimerase deficiency [MIM:251120]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCFD2">
+ <field name="name">MCFD2</field>
+ <field name="long_name">multiple coagulation factor deficiency 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p21-p16.3</field>
+ <field name="info">
+Factor V and factor VIII, combined deficiency of [MIM:227300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCHR1">
+ <field name="name">MCHR1</field>
+ <field name="long_name">melanin-concentrating hormone receptor 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCI2">
+ <field name="name">MCI2</field>
+ <field name="long_name">Myocardial infarction, susceptiblity to, 2</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12</field>
+ <field name="info">
+Myocardial infarction, susceptiblity to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCKD1">
+ <field name="name">MCKD1</field>
+ <field name="long_name">medullary cystic kidney disease 1 (autosomal dominant)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Medullary cystic kidney disease 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCKD2">
+ <field name="name">MCKD2</field>
+ <field name="long_name">medullary cystic kidney disease 2 (autosomal dominant)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12.3</field>
+ <field name="info">
+Hyperuricemic nephropathy, familial juvenile [MIM:162000]
+Medullary cystic kidney disease 2 [MIM:603860]
+Glomerulocystic kidney disease with hyperuricemia and isosthenuria [MIM:609886]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCM6">
+ <field name="name">MCM6</field>
+ <field name="long_name">minichromosome maintenance complex component 6</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q21</field>
+ <field name="info">
+Lactase persistance/nonpersistance [MIM:223100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCOLN1">
+ <field name="name">MCOLN1</field>
+ <field name="long_name">mucolipin 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3-p13.2</field>
+ <field name="info">
+Mucolipidosis IV [MIM:252650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCOR">
+ <field name="name">MCOR</field>
+ <field name="long_name">microcoria, congenital</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q31-q32</field>
+ <field name="info">
+Microcoria, congenital</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCPH1">
+ <field name="name">MCPH1</field>
+ <field name="long_name">microcephalin 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23</field>
+ <field name="info">
+Microcephaly, autosomal recessive 1 [MIM:251200]
+Premature chromosome condensation with microcephaly and mental retardation [MIM:606858]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCPH2">
+ <field name="name">MCPH2</field>
+ <field name="long_name">microcephaly, primary autosomal recessive 2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1-q13.2</field>
+ <field name="info">
+Microcephaly, primary autosomal recessive, 2 [MIM:251200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCPH3">
+ <field name="name">MCPH3</field>
+ <field name="long_name">microcephaly, primary autosomal recessive 3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q33.3</field>
+ <field name="info">
+Microcephaly, primary autosomal recessive, 3 [MIM:604804]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCPH4">
+ <field name="name">MCPH4</field>
+ <field name="long_name">microcephaly, primary autosomal recessive 4</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15-q21</field>
+ <field name="info">
+Microcephaly, primary autosomal recessive, 4 [MIM:251200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCPHA">
+ <field name="name">MCPHA</field>
+ <field name="long_name">microcephaly, Amish</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25.3</field>
+ <field name="info">
+Microcephaly, Amish type [MIM:607196]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MCS">
+ <field name="name">MCS</field>
+ <field name="long_name">Miles-Carpenter X-linked mental retardation syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13-q22</field>
+ <field name="info">
+Mental retardation, X-linked, syndromic-4, with congenital contractures and low fingertip arches</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MDC1B">
+ <field name="name">MDC1B</field>
+ <field name="long_name">Muscular dystrophy, congenital, 1B</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42</field>
+ <field name="info">
+Muscular dystrophy, congenital, 1B</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MDD1">
+ <field name="name">MDD1</field>
+ <field name="long_name">Major depressive disorder</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q22-q23.2</field>
+ <field name="info">
+Major depressive disorder 1 [MIM:608516]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MDD2">
+ <field name="name">MDD2</field>
+ <field name="long_name">Major depressive disorder 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q25.3-q26.2</field>
+ <field name="info">
+Major depressive disorder 2 [MIM:608516]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MDDC">
+ <field name="name">MDDC</field>
+ <field name="long_name">macular dystrophy, dominant cystoid</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p21-p15</field>
+ <field name="info">
+Macular dystrophy, dominant cystoid</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MDH1">
+ <field name="name">MDH1</field>
+ <field name="long_name">malate dehydrogenase 1, NAD (soluble)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p16</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MDM2">
+ <field name="name">MDM2</field>
+ <field name="long_name">Mdm2 p53 binding protein homolog (mouse)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q14.3-q15</field>
+ <field name="info">
+Accelerated tumor formation, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MDRV">
+ <field name="name">MDRV</field>
+ <field name="long_name">muscular dystrophy, with rimmed vacuoles</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Muscular dystrophy with rimmed vacuoles</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MDS1">
+ <field name="name">MDS1</field>
+ <field name="long_name">myelodysplasia syndrome 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26</field>
+ <field name="info">
+Myelodysplasia syndrome-1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ME2">
+ <field name="name">ME2</field>
+ <field name="long_name">malic enzyme 2, NAD(+)-dependent, mitochondrial</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21</field>
+ <field name="info">
+Epilepsy, idopathic generalized, susceptibility to [MIM:600669]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MEAX">
+ <field name="name">MEAX</field>
+ <field name="long_name">myopathy with excessive autophagy</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Myopathy, X-linked, with excessive autophagy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MEB">
+ <field name="name">MEB</field>
+ <field name="long_name">muscle-eye-brain disease</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34-p33</field>
+ <field name="info">
+Muscle-eye-brain disease [MIM:253280]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MECP2">
+ <field name="name">MECP2</field>
+ <field name="long_name">methyl CpG binding protein 2 (Rett syndrome)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Rett syndrome [MIM:312750]
+Mental retardation, X-linked, syndromic 13 [MIM:300055]
+Rett syndrome, preserved speech variant [MIM:312750]
+Encephalopathy, neonatal severe [MIM:300673]
+Autism, susceptibility to, X-linked-3 [MIM:300496]
+Angelman syndrome [MIM:105830]
+Mental retardation, X-linked, Lubs type [MIM:300260]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MED12">
+ <field name="name">MED12</field>
+ <field name="long_name">mediator complex subunit 12</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13</field>
+ <field name="info">
+Opitz-Kaveggia syndrome [MIM:305450]
+Lujan-Fryns syndrome [MIM:309520]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MEF2A">
+ <field name="name">MEF2A</field>
+ <field name="long_name">myocyte enhancer factor 2A</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26</field>
+ <field name="info">
+Coronary artery disease, autosomal dominant, 1 [MIM:608320]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MEFV">
+ <field name="name">MEFV</field>
+ <field name="long_name">Mediterranean fever</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13</field>
+ <field name="info">
+Familial Mediterranean fever, AR [MIM:249100]
+Familial Mediterranean fever, AD [MIM:134610]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MEHMO">
+ <field name="name">MEHMO</field>
+ <field name="long_name">mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly and obesity syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.13-p21.1</field>
+ <field name="info">
+MEHMO syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MEN1">
+ <field name="name">MEN1</field>
+ <field name="long_name">multiple endocrine neoplasia I</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Multiple endocrine neoplasia I
+Hyperparathyroidism, AD [MIM:145000]
+Prolactinoma, hyperparathyroidism, carcinoid syndrome
+Carcinoid tumor of lung
+Parathyroid adenoma, somatic
+Lipoma, somatic
+Angiofibroma, somatic
+Adrenal adenoma, somatic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MENAQ1">
+ <field name="name">MENAQ1</field>
+ <field name="long_name">Menarche, age at, QTL</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13</field>
+ <field name="info">
+Menarche, age at, QTL</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MENOQ1">
+ <field name="name">MENOQ1</field>
+ <field name="long_name">menopause, natural, age at, QTL</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp21.3</field>
+ <field name="info">
+Menopause, natural, age at, QTL</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MEP1B">
+ <field name="name">MEP1B</field>
+ <field name="long_name">meprin A, beta</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q12.2-q12.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MERTK">
+ <field name="name">MERTK</field>
+ <field name="long_name">c-mer proto-oncogene tyrosine kinase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14.1</field>
+ <field name="info">
+Retinitis pigmentosa-38 [MIM:268000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MESP2">
+ <field name="name">MESP2</field>
+ <field name="long_name">mesoderm posterior 2 homolog (mouse)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26.1</field>
+ <field name="info">
+Spondylocostal dysostosis, autosomal recessive 2 [MIM:608681]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MET">
+ <field name="name">MET</field>
+ <field name="long_name">met proto-oncogene (hepatocyte growth factor receptor)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31</field>
+ <field name="info">
+Renal cell carcinoma, papillary, familial and sporadic [MIM:605074]
+Hepatocellular carcinoma, childhood type [MIM:114550]
+Autism, suseptibility to, 9 [MIM:611015]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MFHAS1">
+ <field name="name">MFHAS1</field>
+ <field name="long_name">malignant fibrous histiocytoma amplified sequence 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23.1</field>
+ <field name="info">
+Malignant fibrous histiocytoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MFI2">
+ <field name="name">MFI2</field>
+ <field name="long_name">antigen p97 (melanoma associated) identified by monoclonal antibodies 133.2 and 96.5</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q29</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MFN2">
+ <field name="name">MFN2</field>
+ <field name="long_name">mitofusin 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 2A2 [MIM:609260]
+Hereditary motor and sensory neuropathy VI [MIM:601152]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MFRP">
+ <field name="name">MFRP</field>
+ <field name="long_name">membrane frizzled-related protein</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Microphthalmia, posterior, with retinitis pigmentosa, foveoschisis, and optic disc drusen [MIM:611040]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MFSD8">
+ <field name="name">MFSD8</field>
+ <field name="long_name">major facilitator superfamily domain containing 8</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q28.1-q28.2</field>
+ <field name="info">
+Ceroid lipofuscinosis, neuronal, 7 [MIM:610951]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MFT2">
+ <field name="name">MFT2</field>
+ <field name="long_name">Trichoepithelioma, multiple familial, 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21</field>
+ <field name="info">
+Trichoepithelioma, multiple familial, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGAM">
+ <field name="name">MGAM</field>
+ <field name="long_name">maltase-glucoamylase (alpha-glucosidase)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q34</field>
+ <field name="info">
+diarrhea in children associated with starch malabsorption and small intestinal glucoamylase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGAT2">
+ <field name="name">MGAT2</field>
+ <field name="long_name">mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q21</field>
+ <field name="info">
+Carbohydrate-deficient glycoprotein syndrome, type II [MIM:212066]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGC1">
+ <field name="name">MGC1</field>
+ <field name="long_name">megalocornea 1 (X-linked)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq21.3-q22</field>
+ <field name="info">
+Megalocornea, X-linked</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGCR">
+ <field name="name">MGCR</field>
+ <field name="long_name">meningioma chromosome region</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.3-qter</field>
+ <field name="info">
+Meningioma [MIM:607174]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGCT">
+ <field name="name">MGCT</field>
+ <field name="long_name">male germ cell tumor</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q22</field>
+ <field name="info">
+Male germ cell tumor</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGEA5">
+ <field name="name">MGEA5</field>
+ <field name="long_name">meningioma expressed antigen 5 (hyaluronidase)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24.1-q24.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGMT">
+ <field name="name">MGMT</field>
+ <field name="long_name">O-6-methylguanine-DNA methyltransferase</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q26</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGP">
+ <field name="name">MGP</field>
+ <field name="long_name">matrix Gla protein</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.1-p12.3</field>
+ <field name="info">
+Keutel syndrome [MIM:245150]
+Natural teeth remaining intact</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGR12">
+ <field name="name">MGR12</field>
+ <field name="long_name">Migraine, with or without aura, susceptibility to, 12</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22-q23</field>
+ <field name="info">
+Migraine, with or without aura, susceptibility to, 12</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGR2">
+ <field name="name">MGR2</field>
+ <field name="long_name">Migraine, familial typical, susceptibility to</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq</field>
+ <field name="info">
+Migraine, familial typical, susceptibility to, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGR3">
+ <field name="name">MGR3</field>
+ <field name="long_name">Migraine, familial, with or without aura, susceptibility to</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.1-p12.2</field>
+ <field name="info">
+Migraine with or without aura, susceptibility to, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGR4">
+ <field name="name">MGR4</field>
+ <field name="long_name">Migraine, susceptibility to, 4</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q21.2-q22.3</field>
+ <field name="info">
+Migraine without aura, susceptibility to, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGR5">
+ <field name="name">MGR5</field>
+ <field name="long_name">Migraine with or without aura, susceptibility to, 5</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13</field>
+ <field name="info">
+Migraine with or without aura, susceptibility to, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGR7">
+ <field name="name">MGR7</field>
+ <field name="long_name">Migraine with aura, susceptibility to, 7</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q11.2-q12</field>
+ <field name="info">
+Migraine with aura, susceptibility to, 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGR8">
+ <field name="name">MGR8</field>
+ <field name="long_name">Migraine, susceptibility to, 8</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q21</field>
+ <field name="info">
+Migraine, susceptibility to, 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGST2">
+ <field name="name">MGST2</field>
+ <field name="long_name">microsomal glutathione S-transferase 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q28-q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MGS">
+ <field name="name">MGS</field>
+ <field name="long_name">Mungen syndrome</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q23-q24</field>
+ <field name="info">
+Mungen syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MHAC">
+ <field name="name">MHAC</field>
+ <field name="long_name">microhydranencephaly</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3-p12.1</field>
+ <field name="info">
+Microhydranencephaly</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MHS2">
+ <field name="name">MHS2</field>
+ <field name="long_name">malignant hyperthermia susceptibility 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2-q24</field>
+ <field name="info">
+Malignant hyperthermia susceptibility 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MHS3">
+ <field name="name">MHS3</field>
+ <field name="long_name">Malignant hyperthermia susceptibility 3</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21-q22</field>
+ <field name="info">
+Malignant hyperthermia susceptibility 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MHS4">
+ <field name="name">MHS4</field>
+ <field name="long_name">malignant hyperthermia susceptibility 4</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q13.1</field>
+ <field name="info">
+Malignant hyperthermia susceptibility 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MHS6">
+ <field name="name">MHS6</field>
+ <field name="long_name">malignant hyperthermia susceptibility 6</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p</field>
+ <field name="info">
+Malignant hyperthermia susceptibility 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MHW1">
+ <field name="name">MHW1</field>
+ <field name="long_name">Mental health wellness 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p</field>
+ <field name="info">
+Mental health wellness-1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MHW2">
+ <field name="name">MHW2</field>
+ <field name="long_name">Mental health wellness 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q</field>
+ <field name="info">
+Mental health wellness-2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MIAT">
+ <field name="name">MIAT</field>
+ <field name="long_name">myocardial infarction associated transcript (non-protein coding)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.1</field>
+ <field name="info">
+Myocardial infarction, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MICA">
+ <field name="name">MICA</field>
+ <field name="long_name">MHC class I polypeptide-related sequence A</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MICB">
+ <field name="name">MICB</field>
+ <field name="long_name">MHC class I polypeptide-related sequence B</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MID1">
+ <field name="name">MID1</field>
+ <field name="long_name">midline 1 (Opitz/BBB syndrome)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22</field>
+ <field name="info">
+Opitz G syndrome, type I [MIM:300000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MIF">
+ <field name="name">MIF</field>
+ <field name="long_name">macrophage migration inhibitory factor (glycosylation-inhibiting factor)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+Rheumatoid arthritis, systemic juvenile, susceptibility to [MIM:604302]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MINPP1">
+ <field name="name">MINPP1</field>
+ <field name="long_name">multiple inositol polyphosphate histidine phosphatase, 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23</field>
+ <field name="info">
+Thyroid carcinoma, follicular [MIM:188470]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MIPOL1">
+ <field name="name">MIPOL1</field>
+ <field name="long_name">mirror-image polydactyly 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q13</field>
+ <field name="info">
+Mirror-image polydactyly [MIM:135750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MIP">
+ <field name="name">MIP</field>
+ <field name="long_name">major intrinsic protein of lens fiber</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+Cataract, polymorphic and lamellar [MIM:604219]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MIR196A2">
+ <field name="name">MIR196A2</field>
+ <field name="long_name">microRNA 196a-2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MITF">
+ <field name="name">MITF</field>
+ <field name="long_name">microphthalmia-associated transcription factor</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p14.1-p12.3</field>
+ <field name="info">
+Waardenburg syndrome, type IIA [MIM:193510]
+Waardenburg syndrome/ocular albinism, digenic [MIM:103470]
+Tietz syndrome [MIM:103500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MKKS">
+ <field name="name">MKKS</field>
+ <field name="long_name">McKusick-Kaufman syndrome</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p12</field>
+ <field name="info">
+McKusick-Kaufman syndrome [MIM:236700]
+Bardet-Biedl syndrome 6 [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MKL1">
+ <field name="name">MKL1</field>
+ <field name="long_name">megakaryoblastic leukemia (translocation) 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13</field>
+ <field name="info">
+Megakaryoblastic leukemia, acute</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MKS1">
+ <field name="name">MKS1</field>
+ <field name="long_name">Meckel syndrome, type 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23</field>
+ <field name="info">
+Meckel syndrome, type 1 [MIM:249000]
+Bardet-Biedl syndrome 13 [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MKS2">
+ <field name="name">MKS2</field>
+ <field name="long_name">Meckel syndrome, type 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Meckel syndrome, type 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MLC1">
+ <field name="name">MLC1</field>
+ <field name="long_name">megalencephalic leukoencephalopathy with subcortical cysts 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.33</field>
+ <field name="info">
+Megalencephalic leukoencephalopathy with subcortical cysts [MIM:604004]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MLF1">
+ <field name="name">MLF1</field>
+ <field name="long_name">myeloid leukemia factor 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q25.1</field>
+ <field name="info">
+Leukemia, acute myeloid [MIM:601626]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MLH1">
+ <field name="name">MLH1</field>
+ <field name="long_name">mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.3</field>
+ <field name="info">
+Colorectal cancer, hereditary nonpolyposis, type 2 [MIM:609310]
+Mismatch repair cancer syndrome [MIM:276300]
+Muir-Torre syndrome [MIM:158320]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MLH3">
+ <field name="name">MLH3</field>
+ <field name="long_name">mutL homolog 3 (E. coli)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3</field>
+ <field name="info">
+Colorectal cancer, somatic [MIM:114500]
+Colon cancer, hereditary nonpolypopsis, type 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MLLT3">
+ <field name="name">MLLT3</field>
+ <field name="long_name">myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MLL">
+ <field name="name">MLL</field>
+ <field name="long_name">myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Leukemia, myeloid/lymphoid or mixed-lineage</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MLPH">
+ <field name="name">MLPH</field>
+ <field name="long_name">melanophilin</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37</field>
+ <field name="info">
+Griscelli syndrome, type 3 [MIM:609227]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MLXIPL">
+ <field name="name">MLXIPL</field>
+ <field name="long_name">MLX interacting protein-like</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MLYCD">
+ <field name="name">MLYCD</field>
+ <field name="long_name">malonyl-CoA decarboxylase</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24</field>
+ <field name="info">
+Malonyl-CoA decarboxylase deficiency [MIM:248360]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMAA">
+ <field name="name">MMAA</field>
+ <field name="long_name">methylmalonic aciduria (cobalamin deficiency) cblA type</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q31.1-q31.2</field>
+ <field name="info">
+Methylmalonic aciduria, vitamin B12-responsive [MIM:251100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMAB">
+ <field name="name">MMAB</field>
+ <field name="long_name">methylmalonic aciduria (cobalamin deficiency) cblB type</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24</field>
+ <field name="info">
+Methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type [MIM:251110]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMACHC">
+ <field name="name">MMACHC</field>
+ <field name="long_name">methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34.1</field>
+ <field name="info">
+Methylmalonic aciduria and homocystinuria, cblC type [MIM:277400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMADHC">
+ <field name="name">MMADHC</field>
+ <field name="long_name">methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q23.2</field>
+ <field name="info">
+Homocystinuria, cblD type, variant 1 [MIM:277410]
+Methylmalonic aciduria, cblD type, variant 2 [MIM:277410]
+Methylmalonic aciduria and homocystinuria, cblD type [MIM:277410]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMDFS">
+ <field name="name">MMDFS</field>
+ <field name="long_name">Multiple mitochondrial dysfunctions syndrome</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p14-p13</field>
+ <field name="info">
+Multiple mitochondrial dysfunctions syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMDK">
+ <field name="name">MMDK</field>
+ <field name="long_name">Mesomelic dysplasia, Kantaputra type</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q24-q32</field>
+ <field name="info">
+Mesomelic dysplasia, Kantaputra type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMEDF">
+ <field name="name">MMEDF</field>
+ <field name="long_name">Macrocephaly with multiple epiphyseal dysplasia and distinctive facies</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26.1</field>
+ <field name="info">
+Macrocephaly with multiple epiphyseal dysplasia and distinctive facies</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MME">
+ <field name="name">MME</field>
+ <field name="long_name">membrane metallo-endopeptidase</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21-q27</field>
+ <field name="info">
+Neutral endopeptidase deficiency
+Membranous glomerulonephritis, antenatal</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMP10">
+ <field name="name">MMP10</field>
+ <field name="long_name">matrix metallopeptidase 10 (stromelysin 2)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22.3-q23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMP12">
+ <field name="name">MMP12</field>
+ <field name="long_name">matrix metallopeptidase 12 (macrophage elastase)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22.2-q22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMP13">
+ <field name="name">MMP13</field>
+ <field name="long_name">matrix metallopeptidase 13 (collagenase 3)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22.3</field>
+ <field name="info">
+Spondyloepimetaphyseal dysplasia, Missouri type [MIM:602111]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMP1">
+ <field name="name">MMP1</field>
+ <field name="long_name">matrix metallopeptidase 1 (interstitial collagenase)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22-q23</field>
+ <field name="info">
+COPD, rate of decline of lung function in [MIM:606963]
+Epidermolysis bullosa dystrophica, autosomal recessive, modifier of [MIM:226600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMP20">
+ <field name="name">MMP20</field>
+ <field name="long_name">matrix metallopeptidase 20</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22.3-q23</field>
+ <field name="info">
+Amelogenesis imperfecta, pigmented hypomaturation type [MIM:204700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMP2">
+ <field name="name">MMP2</field>
+ <field name="long_name">matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q13</field>
+ <field name="info">
+Torg-Winchester syndrome [MIM:259600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMP3">
+ <field name="name">MMP3</field>
+ <field name="long_name">matrix metallopeptidase 3 (stromelysin 1, progelatinase)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Coronary heart disease, susceptibility to, 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMP7">
+ <field name="name">MMP7</field>
+ <field name="long_name">matrix metallopeptidase 7 (matrilysin, uterine)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q21-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMP8">
+ <field name="name">MMP8</field>
+ <field name="long_name">matrix metallopeptidase 8 (neutrophil collagenase)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q21-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMP9">
+ <field name="name">MMP9</field>
+ <field name="long_name">matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11.2-q13.1</field>
+ <field name="info">
+Lumbar disc herniation, susceptibility to [MIM:603932]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMS">
+ <field name="name">MMS</field>
+ <field name="long_name">Malignant mesothelioma, susceptibility to</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p</field>
+ <field name="info">
+Malignant mesothelioma, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMVP1">
+ <field name="name">MMVP1</field>
+ <field name="long_name">myxomatous mitral valve prolapse 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12.1-p11.2</field>
+ <field name="info">
+Mitral valve prolapse, myxomatous 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMVP2">
+ <field name="name">MMVP2</field>
+ <field name="long_name">myxomatous mitral valve prolapse 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.4</field>
+ <field name="info">
+Mitral valve prolapse, myxomatous 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MMVP3">
+ <field name="name">MMVP3</field>
+ <field name="long_name">Mitral valve prolapse, myxomatous 3</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q31.3-q32.1</field>
+ <field name="info">
+Mitral valve prolapse, myxomatous 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MN1">
+ <field name="name">MN1</field>
+ <field name="long_name">meningioma (disrupted in balanced translocation) 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.3-qter</field>
+ <field name="info">
+Meningioma [MIM:607174]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MNDEC">
+ <field name="name">MNDEC</field>
+ <field name="long_name">Microtia with nasolacrimal duct imperforation and eye coloboma</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16-p15</field>
+ <field name="info">
+Microtia with nasolacrimal duct imperforation and eye coloboma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MNG1">
+ <field name="name">MNG1</field>
+ <field name="long_name">multinodular goitre 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q</field>
+ <field name="info">
+Goiter, multinodular, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MNG2">
+ <field name="name">MNG2</field>
+ <field name="long_name">multinodular goiter 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22</field>
+ <field name="info">
+Goiter, multinodular, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MNG3">
+ <field name="name">MNG3</field>
+ <field name="long_name">Multinodular goiter-3</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.1-q26.3</field>
+ <field name="info">
+Goiter, multinodular, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MNRI">
+ <field name="name">MNRI</field>
+ <field name="long_name">meningioma, radiation-induced</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p11</field>
+ <field name="info">
+Meningioma, radiation-induced</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MOCS1">
+ <field name="name">MOCS1</field>
+ <field name="long_name">molybdenum cofactor synthesis 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Molybdenum cofactor deficiency, type A [MIM:252150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MOCS2">
+ <field name="name">MOCS2</field>
+ <field name="long_name">molybdenum cofactor synthesis 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q11</field>
+ <field name="info">
+Molybdenum cofactor deficiency, type B [MIM:252150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MOPD1">
+ <field name="name">MOPD1</field>
+ <field name="long_name">Taybi-Linder syndrome</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q14.2-q14.3</field>
+ <field name="info">
+Taybi-Linder syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPD2">
+ <field name="name">MPD2</field>
+ <field name="long_name">myopathy, distal 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q</field>
+ <field name="info">
+Myopathy, distal</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPD3">
+ <field name="name">MPD3</field>
+ <field name="long_name">Myopathy, distal 3</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p22-q11</field>
+ <field name="info">
+Myopathy, distal 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPDMRS">
+ <field name="name">MPDMRS</field>
+ <field name="long_name">Martin-Probst deafness-mental retardation syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq11-q21</field>
+ <field name="info">
+Martin-Probst deafness-mental retardation syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPDU1">
+ <field name="name">MPDU1</field>
+ <field name="long_name">mannose-P-dolichol utilization defect 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.1-p12</field>
+ <field name="info">
+Congenital disorder of glycosylation, type If [MIM:609180]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPG">
+ <field name="name">MPG</field>
+ <field name="long_name">N-methylpurine-DNA glycosylase</field>
+ <field name="chromosome">16</field>
+ <field name="location">16pter-p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPI">
+ <field name="name">MPI</field>
+ <field name="long_name">mannose phosphate isomerase</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22-qter</field>
+ <field name="info">
+Carbohydrate-deficient glycoprotein syndrome, type Ib [MIM:602579]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPL">
+ <field name="name">MPL</field>
+ <field name="long_name">myeloproliferative leukemia virus oncogene</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34</field>
+ <field name="info">
+Thrombocytopenia, congenital amegakaryocytic [MIM:604498]
+Thrombycytosis, susceptibility to [MIM:187950]
+Thrombocythemia, essential [MIM:187950]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPO">
+ <field name="name">MPO</field>
+ <field name="long_name">myeloperoxidase</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23.1</field>
+ <field name="info">
+Myeloperoxidase deficiency [MIM:254600]
+Alzheimer disease, susceptibility to [MIM:104300]
+Lung cancer, protection against, in smokers (3) 11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPP3">
+ <field name="name">MPP3</field>
+ <field name="long_name">membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12-q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPST">
+ <field name="name">MPST</field>
+ <field name="long_name">mercaptopyruvate sulfurtransferase</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2-qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPV17">
+ <field name="name">MPV17</field>
+ <field name="long_name">MpV17 mitochondrial inner membrane protein</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p23-p21</field>
+ <field name="info">
+Mitochondrial DNA depletion syndrome, hepatocerebral form [MIM:251880]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPVQTL1">
+ <field name="name">MPVQTL1</field>
+ <field name="long_name">Mean platelet volume QTL1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.31</field>
+ <field name="info">
+Mean platelet volume QTL1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPVQTL2">
+ <field name="name">MPVQTL2</field>
+ <field name="long_name">Mean platelet volume QTL2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21-p13</field>
+ <field name="info">
+Mean platelet volume QTL2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPVQTL3">
+ <field name="name">MPVQTL3</field>
+ <field name="long_name">Mean platelet volume QTL3</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2</field>
+ <field name="info">
+Mean platelet volume QTL3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MPZ">
+ <field name="name">MPZ</field>
+ <field name="long_name">myelin protein zero</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q22</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 1B [MIM:118200]
+Dejerine-Sottas syndrome [MIM:145900]
+Neuropathy, congenital hypomyelinating [MIM:605253]
+Charcot-Marie-Tooth disease, type 2J [MIM:607736]
+Roussy-Levy syndrome [MIM:180800]
+Charcot-Marie-Tooth disease, type 2I [MIM:607677]
+Charcot-Marie-Tooth disease, dominant intermediate 3 [MIM:607791]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRAP">
+ <field name="name">MRAP</field>
+ <field name="long_name">melanocortin 2 receptor accessory protein</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.1</field>
+ <field name="info">
+Glucocorticoid deficiency 2 [MIM:607398]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRE11A">
+ <field name="name">MRE11A</field>
+ <field name="long_name">MRE11 meiotic recombination 11 homolog A (S. cerevisiae)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q21</field>
+ <field name="info">
+Ataxia-telangiectasia-like disorder [MIM:604391]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MROS">
+ <field name="name">MROS</field>
+ <field name="long_name">Melkersson-Rosenthal syndrome</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p11</field>
+ <field name="info">
+Melkersson-Rosenthal syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRPS16">
+ <field name="name">MRPS16</field>
+ <field name="long_name">mitochondrial ribosomal protein S16</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.1</field>
+ <field name="info">
+Combined oxidative phosphorylation deficiency 2 [MIM:610498]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRPS22">
+ <field name="name">MRPS22</field>
+ <field name="long_name">mitochondrial ribosomal protein S22</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q23</field>
+ <field name="info">
+Combined oxidative phosphorylation deficiency 5 [MIM:611719]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRSD">
+ <field name="name">MRSD</field>
+ <field name="long_name">mental retardation-skeletal dysplasia</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Mental retardation-skeletal dysplasia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRSS">
+ <field name="name">MRSS</field>
+ <field name="long_name">Mental retardation, X-linked, with short stature</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24</field>
+ <field name="info">
+Mental retardation, X-linked, with short stature</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRST">
+ <field name="name">MRST</field>
+ <field name="long_name">Mental retardation, severe, with spasticity and tapetoretinal</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q24</field>
+ <field name="info">
+Mental retardation, severe, with spasticity and tapetoretinal degeneration</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRT10">
+ <field name="name">MRT10</field>
+ <field name="long_name">Mental retardation, autosomal recessive, 10</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12-q12</field>
+ <field name="info">
+Mental retardation, autosomal recessive, 10</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRT11">
+ <field name="name">MRT11</field>
+ <field name="long_name">Mental retardation, autosomal recessive, 11</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2-q13.3</field>
+ <field name="info">
+Mental retardation, autosomal recessive, 11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRT12">
+ <field name="name">MRT12</field>
+ <field name="long_name">Mental retardation, autosomal recessive, 12</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34-p33</field>
+ <field name="info">
+Mental retardation, autosomal recessive, 12</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRT4">
+ <field name="name">MRT4</field>
+ <field name="long_name">mental retardation, non-syndromic, autosomal recessive, 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p21.1-p13.3</field>
+ <field name="info">
+Mental retardation, autosomal recessive, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRT5">
+ <field name="name">MRT5</field>
+ <field name="long_name">Mental retardaion, autosomal recessive, 5</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15-p14</field>
+ <field name="info">
+Mental retardaion, autosomal recessive, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRT8">
+ <field name="name">MRT8</field>
+ <field name="long_name">Mental retardation, autosomal recessive, 8</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22</field>
+ <field name="info">
+Mental retardation, autosomal recessive, 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRT9">
+ <field name="name">MRT9</field>
+ <field name="long_name">Mental retardation, autosomal recessive, 9</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2-q12</field>
+ <field name="info">
+Mental retardation, autosomal recessive, 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX14">
+ <field name="name">MRX14</field>
+ <field name="long_name">mental retardation, X-linked 14</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.3-q13.3</field>
+ <field name="info">
+Mental retardation, X-linked 14</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX17">
+ <field name="name">MRX17</field>
+ <field name="long_name">mental retardation, X-linked 17</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.2</field>
+ <field name="info">
+2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency [MIM:300438]
+Mental retardation, X-linked syndromic 10 [MIM:300220]
+Mental retardation, X-linked 17/31, microduplication [MIM:300705]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX1">
+ <field name="name">MRX1</field>
+ <field name="long_name">mental retardation, X-linked 1 (non-dysmorphic)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.3-q21.1</field>
+ <field name="info">
+Mental retardation, X-linked, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX20">
+ <field name="name">MRX20</field>
+ <field name="long_name">mental retardation, X-linked 20</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11-q21</field>
+ <field name="info">
+Mental retardation, X-linked 20</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX23">
+ <field name="name">MRX23</field>
+ <field name="long_name">mental retardation, X-linked 23</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq23-q24</field>
+ <field name="info">
+Mental retardation, X-linked 23, nonspecific</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX27">
+ <field name="name">MRX27</field>
+ <field name="long_name">mental retardation, X-linked 27</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq23-q24</field>
+ <field name="info">
+Mental retardation, X-linked 23, nonspecific</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX2">
+ <field name="name">MRX2</field>
+ <field name="long_name">mental retardation, X-linked 2 (non-dysmorphic)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3</field>
+ <field name="info">
+Mental retardation, X-linked, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX31">
+ <field name="name">MRX31</field>
+ <field name="long_name">mental retardation, X-linked 31</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.2</field>
+ <field name="info">
+2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency [MIM:300438]
+Mental retardation, X-linked syndromic 10 [MIM:300220]
+Mental retardation, X-linked 17/31, microduplication [MIM:300705]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX35">
+ <field name="name">MRX35</field>
+ <field name="long_name">mental retardation, X-linked 35</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq23-q24</field>
+ <field name="info">
+Mental retardation, X-linked 23, nonspecific</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX42">
+ <field name="name">MRX42</field>
+ <field name="long_name">mental retardation, X-linked 42</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26</field>
+ <field name="info">
+Mental retardation, X-linked nonspecific, 42</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX49">
+ <field name="name">MRX49</field>
+ <field name="long_name">mental retardation, X-linked 49</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3</field>
+ <field name="info">
+Mental retardation, X-linked-49</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX50">
+ <field name="name">MRX50</field>
+ <field name="long_name">mental retardation, X-linked 50</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.3-p11.21</field>
+ <field name="info">
+Mental retardation, X-linked nonspecific, type 50</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX52">
+ <field name="name">MRX52</field>
+ <field name="long_name">mental retardation, X-linked 52</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.21-q22.3</field>
+ <field name="info">
+Mental retardation, X-linked 52</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX53">
+ <field name="name">MRX53</field>
+ <field name="long_name">mental retardation, X-linked 53</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22.2-q26</field>
+ <field name="info">
+Mental retardation, X-linked-53</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX72">
+ <field name="name">MRX72</field>
+ <field name="long_name">mental retardation, X-linked 72</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Mental retardation, X-linked-72</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX77">
+ <field name="name">MRX77</field>
+ <field name="long_name">mental retardation, X-linked 77</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq12-q21.3</field>
+ <field name="info">
+Mental retardation, X-linked 77</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX78">
+ <field name="name">MRX78</field>
+ <field name="long_name">mental retardation, X-linked 78</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.4-p11.23</field>
+ <field name="info">
+Mental retardation, X-linked 78</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX80">
+ <field name="name">MRX80</field>
+ <field name="long_name">mental retardation, X-linked 80</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq23-q24</field>
+ <field name="info">
+Mental retardation, X-linked 23, nonspecific</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX81">
+ <field name="name">MRX81</field>
+ <field name="long_name">mental retardation, X-linked 81</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.2-q12</field>
+ <field name="info">
+Mental retardation, X-linked 81</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX82">
+ <field name="name">MRX82</field>
+ <field name="long_name">mental retardation, X-linked 82</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24-q25</field>
+ <field name="info">
+Mental retardation, X-linked 82</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRX84">
+ <field name="name">MRX84</field>
+ <field name="long_name">mental retardation, X-linked 84</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.3-q22.3</field>
+ <field name="info">
+Mental retardation, X-linked 84</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRXS10">
+ <field name="name">MRXS10</field>
+ <field name="long_name">mental retardation, X-linked, syndromic 10</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.2</field>
+ <field name="info">
+2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency [MIM:300438]
+Mental retardation, X-linked syndromic 10 [MIM:300220]
+Mental retardation, X-linked 17/31, microduplication [MIM:300705]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRXS11">
+ <field name="name">MRXS11</field>
+ <field name="long_name">mental retardation, X-linked, syndromic 11</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26-q27</field>
+ <field name="info">
+Mental retardation, X-linked, Shashi type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRXS12">
+ <field name="name">MRXS12</field>
+ <field name="long_name">Mental retardation, X-linked, syndromic 12</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11</field>
+ <field name="info">
+Mental retardation, X-linked, syndromic 12</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRXS5">
+ <field name="name">MRXS5</field>
+ <field name="long_name">mental retardation, X-linked, syndromic 5</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq25-q27</field>
+ <field name="info">
+Mental retardation, X-linked, syndromic-5, with Dandy-Walker malformation, basal ganglia disease, and seizures</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRXS7">
+ <field name="name">MRXS7</field>
+ <field name="long_name">mental retardation, X-linked, syndromic 7</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.3-q22</field>
+ <field name="info">
+Mental retardation, X-linked, syndromic 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRXSAB">
+ <field name="name">MRXSAB</field>
+ <field name="long_name">Abidi X-linked mental retardation syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.2</field>
+ <field name="info">
+Mental retardation syndrome, X-linked, Abidi type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRXSA">
+ <field name="name">MRXSA</field>
+ <field name="long_name">Armfield X-linked mental retardation syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Mental retardation syndrome, X-linked, Armfield type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MRXSL">
+ <field name="name">MRXSL</field>
+ <field name="long_name">Lubs X-linked mental retardation syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Mental retardation syndrome, X-linked, Lubs type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MS2">
+ <field name="name">MS2</field>
+ <field name="long_name">Multiple sclerosis, susceptibility to, 2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p15.1</field>
+ <field name="info">
+Multiple sclerosis, susceptibility to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MS3">
+ <field name="name">MS3</field>
+ <field name="long_name">Multiple sclerosis, susceptibility to, 3</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13.2</field>
+ <field name="info">
+Multiple sclerosis, susceptibility to, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MS4A12">
+ <field name="name">MS4A12</field>
+ <field name="long_name">membrane-spanning 4-domains, subfamily A, member 12</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q12-q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MS4A2">
+ <field name="name">MS4A2</field>
+ <field name="long_name">membrane-spanning 4-domains, subfamily A, member 2 (Fc fragment of IgE, high affinity I, receptor for; beta polypeptide)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Atopy, susceptibility to [MIM:147050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MS4A6A">
+ <field name="name">MS4A6A</field>
+ <field name="long_name">membrane-spanning 4-domains, subfamily A, member 6A</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q12-q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MS4">
+ <field name="name">MS4</field>
+ <field name="long_name">Multiple sclerosis, susceptiblity to, 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Multiple sclerosis, susceptiblity to, 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MSH2">
+ <field name="name">MSH2</field>
+ <field name="long_name">mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p22-p21</field>
+ <field name="info">
+Colorectal cancer, hereditary nonpolyposis, type 1 [MIM:120435]
+Muir-Torre syndrome [MIM:158320]
+Mismatch repair cancer syndrome [MIM:276300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MSH3">
+ <field name="name">MSH3</field>
+ <field name="long_name">mutS homolog 3 (E. coli)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q11-q12</field>
+ <field name="info">
+Endometrial carcinoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MSH4">
+ <field name="name">MSH4</field>
+ <field name="long_name">mutS homolog 4 (E. coli)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MSH6">
+ <field name="name">MSH6</field>
+ <field name="long_name">mutS homolog 6 (E. coli)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p16</field>
+ <field name="info">
+Colorectal cancer, hereditary nonpolyposis, type 5
+Endometrial cancer, familial [MIM:608089]
+Mismatch repair cancer syndrome [MIM:276300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MSMB">
+ <field name="name">MSMB</field>
+ <field name="long_name">microseminoprotein, beta-</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q11.2</field>
+ <field name="info">
+Prostate cancer, hereditary, 13 [MIM:611928]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MSR1">
+ <field name="name">MSR1</field>
+ <field name="long_name">macrophage scavenger receptor 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p22</field>
+ <field name="info">
+Prostate cancer, hereditary [MIM:176807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MSSE">
+ <field name="name">MSSE</field>
+ <field name="long_name">multiple self-healing squamous epithelioma</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q31</field>
+ <field name="info">
+Epithelioma, self-healing, squamous 1, Ferguson-Smith type
+Basal cell carcinoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MST1R">
+ <field name="name">MST1R</field>
+ <field name="long_name">macrophage stimulating 1 receptor (c-met-related tyrosine kinase)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MSTN">
+ <field name="name">MSTN</field>
+ <field name="long_name">myostatin</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q32.2</field>
+ <field name="info">
+Muscle hypertrophy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MSX1">
+ <field name="name">MSX1</field>
+ <field name="long_name">msh homeobox 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.1</field>
+ <field name="info">
+Tooth agenesis, selective, 1, with or without orofacial cleft [MIM:106600]
+Witkop syndrome [MIM:189500]
+Orofacial cleft 5 [MIM:608874]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MSX2">
+ <field name="name">MSX2</field>
+ <field name="long_name">msh homeobox 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q34-q35</field>
+ <field name="info">
+Craniosynostosis, type 2 [MIM:604757]
+Parietal foramina 1 [MIM:168500]
+Parietal foramina with cleidocranial dysplasia [MIM:168550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MT1A">
+ <field name="name">MT1A</field>
+ <field name="long_name">metallothionein 1A</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MT2A">
+ <field name="name">MT2A</field>
+ <field name="long_name">metallothionein 2A</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MTAP">
+ <field name="name">MTAP</field>
+ <field name="long_name">methylthioadenosine phosphorylase</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MTBS1">
+ <field name="name">MTBS1</field>
+ <field name="long_name">mycobacterium tuberculosis, susceptibility to infection by, 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35</field>
+ <field name="info">
+Tuberculosis, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MTBS2">
+ <field name="name">MTBS2</field>
+ <field name="long_name">Mycobacterium tuberculosis, susceptibility to, 2</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q12-q13</field>
+ <field name="info">
+Mycobacterium tuberculosis, susceptibility to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MTCP1">
+ <field name="name">MTCP1</field>
+ <field name="long_name">mature T-cell proliferation 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+prolymphocytic leukemia (T-PLL),with translocation t(X;14)(q28;q11) and breakpoint at MTCP1 locus</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MTHFR">
+ <field name="name">MTHFR</field>
+ <field name="long_name">5,10-methylenetetrahydrofolate reductase (NADPH)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3</field>
+ <field name="info">
+Homocystinuria due to MTHFR deficiency [MIM:236250]
+Schizophrenia, susceptibility to [MIM:181500]
+Vascular disease, susceptiblity to
+Neural tube defects, susceptiblity to [MIM:601634]
+Cleft lip/palate, susceptibility to [MIM:119530]
+Thromboembolism, susceptibility to [MIM:188050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MTM1">
+ <field name="name">MTM1</field>
+ <field name="long_name">myotubularin 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Myotubular myopathy, X-linked [MIM:310400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MTMR14">
+ <field name="name">MTMR14</field>
+ <field name="long_name">myotubularin related protein 14</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25.3</field>
+ <field name="info">
+Centronuclear myopathy, autosomal, modifier of [MIM:160150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MTMR2">
+ <field name="name">MTMR2</field>
+ <field name="long_name">myotubularin related protein 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 4B1 [MIM:601382]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MTMR9">
+ <field name="name">MTMR9</field>
+ <field name="long_name">myotubularin related protein 9</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23-p22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MTNR1A">
+ <field name="name">MTNR1A</field>
+ <field name="long_name">melatonin receptor 1A</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q35.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MTNR1B">
+ <field name="name">MTNR1B</field>
+ <field name="long_name">melatonin receptor 1B</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q21-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MTRR">
+ <field name="name">MTRR</field>
+ <field name="long_name">5-methyltetrahydrofolate-homocysteine methyltransferase reductase</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.3-p15.2</field>
+ <field name="info">
+Homocystinuria-megaloblastic anemia, cbl E type [MIM:236270]
+Neural tube defects, folate-sensitive, susceptibility to [MIM:601634]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MTR">
+ <field name="name">MTR</field>
+ <field name="long_name">5-methyltetrahydrofolate-homocysteine methyltransferase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q43</field>
+ <field name="info">
+Methylcobalamin deficiency, cblG type [MIM:250940]
+Neural tube defects, folate-sensitive, susceptibility to [MIM:601634]
+Down syndrome, susceptibility to [MIM:190685]
+Cleft lip/palate, susceptibility to [MIM:119530]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MUC13">
+ <field name="name">MUC13</field>
+ <field name="long_name">mucin 13, cell surface associated</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MUC2">
+ <field name="name">MUC2</field>
+ <field name="long_name">mucin 2, oligomeric mucus/gel-forming</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MUC3A">
+ <field name="name">MUC3A</field>
+ <field name="long_name">mucin 3A, cell surface associated</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22</field>
+ <field name="info">
+Ulcerative colitis, susceptibility to [MIM:191390]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MUC4">
+ <field name="name">MUC4</field>
+ <field name="long_name">mucin 4, cell surface associated</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q29</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MUC7">
+ <field name="name">MUC7</field>
+ <field name="long_name">mucin 7, secreted</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q13-q21</field>
+ <field name="info">
+Asthma, protection against [MIM:600807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MUSK">
+ <field name="name">MUSK</field>
+ <field name="long_name">muscle, skeletal, receptor tyrosine kinase</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q31.3-q32</field>
+ <field name="info">
+Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency [MIM:608931]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MUSQTL1">
+ <field name="name">MUSQTL1</field>
+ <field name="long_name">Musical aptitude QTL 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q22</field>
+ <field name="info">
+Musical aptitude QTL 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MUSTQTL1">
+ <field name="name">MUSTQTL1</field>
+ <field name="long_name">Muscle strength quantitative trait locus 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3</field>
+ <field name="info">
+Muscle strength quantitative trait locus 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MUTYH">
+ <field name="name">MUTYH</field>
+ <field name="long_name">mutY homolog (E. coli)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34.3-p32.1</field>
+ <field name="info">
+Adenomas, multiple colorectal [MIM:608456]
+Gastric cancer, somatic [MIM:137215]
+Colorectal adenomatous polyposis, autosomal recessive, with pilomatricomas [MIM:132600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MUT">
+ <field name="name">MUT</field>
+ <field name="long_name">methylmalonyl Coenzyme A mutase</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21</field>
+ <field name="info">
+Methylmalonic aciduria, mut(0) type [MIM:251000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MVK">
+ <field name="name">MVK</field>
+ <field name="long_name">mevalonate kinase</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24</field>
+ <field name="info">
+Mevalonic aciduria [MIM:610377]
+Hyper-IgD syndrome [MIM:260920]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MX1">
+ <field name="name">MX1</field>
+ <field name="long_name">myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse)</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MXI1">
+ <field name="name">MXI1</field>
+ <field name="long_name">MAX interactor 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q25</field>
+ <field name="info">
+Neurofibrosarcoma
+Prostate cancer, susceptibility to [MIM:176807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYAS1">
+ <field name="name">MYAS1</field>
+ <field name="long_name">Myasthenia gravis with thymus hyperplasia</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Myasthenia gravis with thymus hyperplasia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYBL2">
+ <field name="name">MYBL2</field>
+ <field name="long_name">v-myb myeloblastosis viral oncogene homolog (avian)-like 2</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYBPC1">
+ <field name="name">MYBPC1</field>
+ <field name="long_name">myosin binding protein C, slow type</field>
+ <field name="chromosome">12</field>
+ <field name="location">12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYBPC3">
+ <field name="name">MYBPC3</field>
+ <field name="long_name">myosin binding protein C, cardiac</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p11.2</field>
+ <field name="info">
+Cardiomyopathy, familial hypertrophic, 4 [MIM:115197]
+Cardiomyopathy, dilated [MIM:115200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYB">
+ <field name="name">MYB</field>
+ <field name="long_name">v-myb myeloblastosis viral oncogene homolog (avian)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q22</field>
+ <field name="info">
+T-cell acute lymphoblastic leukemia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYCN">
+ <field name="name">MYCN</field>
+ <field name="long_name">v-myc myelocytomatosis viral related oncogene, neuroblastoma derived (avian)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p24.1</field>
+ <field name="info">
+Feingold syndrome [MIM:164280]
+Microcephaly and digital abnormalities with normal intelligence [MIM:602585]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYC">
+ <field name="name">MYC</field>
+ <field name="long_name">v-myc myelocytomatosis viral oncogene homolog (avian)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.12-q24.13</field>
+ <field name="info">
+Burkitt lymphoma [MIM:113970]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYD88">
+ <field name="name">MYD88</field>
+ <field name="long_name">myeloid differentiation primary response gene (88)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p22-p21.3</field>
+ <field name="info">
+Pyogenic bacterial infections, recurrent, due to MYD88 deficiency [MIM:612260]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYF6">
+ <field name="name">MYF6</field>
+ <field name="long_name">myogenic factor 6 (herculin)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q21</field>
+ <field name="info">
+Myopathy, centronuclear [MIM:160150]
+Becker muscular dystrophy modifier [MIM:310200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYH11">
+ <field name="name">MYH11</field>
+ <field name="long_name">myosin, heavy chain 11, smooth muscle</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.13-p13.12</field>
+ <field name="info">
+Aortic aneurysm, familial thoracic 4 [MIM:132900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYH13">
+ <field name="name">MYH13</field>
+ <field name="long_name">myosin, heavy chain 13, skeletal muscle</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.1-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYH14">
+ <field name="name">MYH14</field>
+ <field name="long_name">myosin, heavy chain 14</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.33</field>
+ <field name="info">
+Deafness, autosomal dominant 4 [MIM:600652]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYH15">
+ <field name="name">MYH15</field>
+ <field name="long_name">myosin, heavy chain 15</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q13.13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYH2">
+ <field name="name">MYH2</field>
+ <field name="long_name">myosin, heavy chain 2, skeletal muscle, adult</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.1</field>
+ <field name="info">
+Inclusion body myopathy-3 [MIM:605637]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYH3">
+ <field name="name">MYH3</field>
+ <field name="long_name">myosin, heavy chain 3, skeletal muscle, embryonic</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.1</field>
+ <field name="info">
+Arthrogryposis, distal, type 2A [MIM:193700]
+Arthrogryposis, distal, type 2B [MIM:601680]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYH6">
+ <field name="name">MYH6</field>
+ <field name="long_name">myosin, heavy chain 6, cardiac muscle, alpha</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q12</field>
+ <field name="info">
+Cardiomyopathy, familial hypertrophic [MIM:192600]
+Atrial septal defect 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYH7">
+ <field name="name">MYH7</field>
+ <field name="long_name">myosin, heavy chain 7, cardiac muscle, beta</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q12</field>
+ <field name="info">
+Cardiomyopathy, familial hypertrophic, 1 [MIM:192600]
+Cardiomyopathy, dilated, 1S
+Myopathy, myosin storage [MIM:608358]
+Myopathy, Laing distal [MIM:160500]
+Scapuloperoneal syndrome, myopathic type [MIM:181430]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYH8">
+ <field name="name">MYH8</field>
+ <field name="long_name">myosin, heavy chain 8, skeletal muscle, perinatal</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.1</field>
+ <field name="info">
+Carney complex variant [MIM:608837]
+Trismus-pseudocamptodactyly syndrome [MIM:158300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYH9">
+ <field name="name">MYH9</field>
+ <field name="long_name">myosin, heavy chain 9, non-muscle</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+May-Hegglin anomaly [MIM:155100]
+Fechtner syndrome [MIM:153640]
+Sebastian syndrome [MIM:605249]
+Deafness, autosomal dominant 17 [MIM:603622]
+Epstein syndrome [MIM:153650]
+Macrothrombocytopenia and progressive sensorineural deafness [MIM:600208]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYL2">
+ <field name="name">MYL2</field>
+ <field name="long_name">myosin, light chain 2, regulatory, cardiac, slow</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q23-q24.3</field>
+ <field name="info">
+Cardiomyopathy, hypertrophic, mid-left ventricular chamber type [MIM:608758]
+Cardiomyopathy, familial hypertrophic, 10 [MIM:608758]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYL3">
+ <field name="name">MYL3</field>
+ <field name="long_name">myosin, light chain 3, alkali; ventricular, skeletal, slow</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p</field>
+ <field name="info">
+Cardiomyopathy, familial hypertrophic, 8 [MIM:608751]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYLK2">
+ <field name="name">MYLK2</field>
+ <field name="long_name">myosin light chain kinase 2</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.3</field>
+ <field name="info">
+Cardiomyopathy, hypertrophic, midventricular, digenic [MIM:192600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYMY1">
+ <field name="name">MYMY1</field>
+ <field name="long_name">moyamoya disease 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26-p24.2</field>
+ <field name="info">
+Moyamoya disease</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYMY2">
+ <field name="name">MYMY2</field>
+ <field name="long_name">moyamoya disease 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+Moyamoya disease 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYMY3">
+ <field name="name">MYMY3</field>
+ <field name="long_name">moyamoya disease 3</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q23</field>
+ <field name="info">
+Moyamoya disease 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYO15A">
+ <field name="name">MYO15A</field>
+ <field name="long_name">myosin XVA</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+Deafness, autosomal recessive 3 [MIM:600316]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYO18B">
+ <field name="name">MYO18B</field>
+ <field name="long_name">myosin XVIIIB</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYO1A">
+ <field name="name">MYO1A</field>
+ <field name="long_name">myosin IA</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13-q15</field>
+ <field name="info">
+Deafness, autosomal dominant nonsyndromic sensorineural [MIM:607841]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYO1C">
+ <field name="name">MYO1C</field>
+ <field name="long_name">myosin IC</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYO1F">
+ <field name="name">MYO1F</field>
+ <field name="long_name">myosin IF</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3-p13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYO3A">
+ <field name="name">MYO3A</field>
+ <field name="long_name">myosin IIIA</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p11.1</field>
+ <field name="info">
+Deafness, autosomal recessive 30 [MIM:607101]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYO5A">
+ <field name="name">MYO5A</field>
+ <field name="long_name">myosin VA (heavy chain 12, myoxin)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21</field>
+ <field name="info">
+Griscelli syndrome, type 1 [MIM:214450]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYO5B">
+ <field name="name">MYO5B</field>
+ <field name="long_name">myosin VB</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21</field>
+ <field name="info">
+Microvillus inclusion disease [MIM:251850]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYO6">
+ <field name="name">MYO6</field>
+ <field name="long_name">myosin VI</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q13</field>
+ <field name="info">
+Deafness, autosomal dominant 22 [MIM:606346]
+Deafness, autosomal recessive 37 [MIM:607821]
+Deafness, sensorineural, with hypertrophic cardiomyopathy [MIM:606346]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYO7A">
+ <field name="name">MYO7A</field>
+ <field name="long_name">myosin VIIA</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.5</field>
+ <field name="info">
+Usher syndrome, type 1B [MIM:276900]
+Deafness, autosomal recessive 2, neurosensory [MIM:600060]
+Deafness, autosomal dominant 11, neurosensory [MIM:601317]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYO9B">
+ <field name="name">MYO9B</field>
+ <field name="long_name">myosin IXB</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.1</field>
+ <field name="info">
+Celiac disease, susceptibility to, 4 [MIM:609753]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYOCD">
+ <field name="name">MYOCD</field>
+ <field name="long_name">myocardin</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYOC">
+ <field name="name">MYOC</field>
+ <field name="long_name">myocilin, trabecular meshwork inducible glucocorticoid response</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q24.3-q25.2</field>
+ <field name="info">
+Glaucoma 1A, primary open angle, juvenile-onset [MIM:137750]
+Glaucoma 1A, primary open angle, recessive
+Glaucoma, early-onset, digenic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYOT">
+ <field name="name">MYOT</field>
+ <field name="long_name">myotilin</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Muscular dystrophy, limb-girdle, type 1A [MIM:159000]
+Myotilinopathy [MIM:609200]
+Myopathy, spheroid body [MIM:182920]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYOZ2">
+ <field name="name">MYOZ2</field>
+ <field name="long_name">myozenin 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q26-q27</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP10">
+ <field name="name">MYP10</field>
+ <field name="long_name">myopia 10</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23</field>
+ <field name="info">
+Myopia 10</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP11">
+ <field name="name">MYP11</field>
+ <field name="long_name">myopia 11 (high grade, autosomal dominant)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q22-q27</field>
+ <field name="info">
+Myopia 11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP12">
+ <field name="name">MYP12</field>
+ <field name="long_name">myopia 12 (high grade, autosomal dominant)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.1</field>
+ <field name="info">
+Myopia 12</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP15">
+ <field name="name">MYP15</field>
+ <field name="long_name">myopia 15</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21.1</field>
+ <field name="info">
+Myopia 15</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP16">
+ <field name="name">MYP16</field>
+ <field name="long_name">myopia 16</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.33-p15.2</field>
+ <field name="info">
+Myopia 16</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP1">
+ <field name="name">MYP1</field>
+ <field name="long_name">myopia 1 (X-linked)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Myopia-1
+Bornholm eye disease</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP2">
+ <field name="name">MYP2</field>
+ <field name="long_name">myopia 2 (high grade, autosomal dominant)</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.31</field>
+ <field name="info">
+Myopia-2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP3">
+ <field name="name">MYP3</field>
+ <field name="long_name">myopia 3 (high grade, autosomal dominant)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q21-q23</field>
+ <field name="info">
+Myopia-3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP4">
+ <field name="name">MYP4</field>
+ <field name="long_name">myopia 4 (high grade, autosomal dominant)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15</field>
+ <field name="info">
+Myopia 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP5">
+ <field name="name">MYP5</field>
+ <field name="long_name">myopia 5 (high grade, autosomal dominant)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+Myopia 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP6">
+ <field name="name">MYP6</field>
+ <field name="long_name">myopia 6</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12</field>
+ <field name="info">
+Myopia-6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP7">
+ <field name="name">MYP7</field>
+ <field name="long_name">myopia 7</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13</field>
+ <field name="info">
+Myopia 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP8">
+ <field name="name">MYP8</field>
+ <field name="long_name">myopia 8</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26</field>
+ <field name="info">
+Myopia 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="MYP9">
+ <field name="name">MYP9</field>
+ <field name="long_name">myopia 9</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q12</field>
+ <field name="info">
+Myopia 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NAGA">
+ <field name="name">NAGA</field>
+ <field name="long_name">N-acetylgalactosaminidase, alpha-</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11</field>
+ <field name="info">
+Schindler disease, type I [MIM:609241]
+Kanzaki disease [MIM:609242]
+Schindler disease, type III [MIM:609241]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NAGLU">
+ <field name="name">NAGLU</field>
+ <field name="long_name">N-acetylglucosaminidase, alpha-</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+Sanfilippo syndrome, type B [MIM:252920]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NAGS">
+ <field name="name">NAGS</field>
+ <field name="long_name">N-acetylglutamate synthase</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.31</field>
+ <field name="info">
+N-acetylglutamate synthase deficiency [MIM:237310]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NAIP">
+ <field name="name">NAIP</field>
+ <field name="long_name">NLR family, apoptosis inhibitory protein</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q12.2-q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NAMSD">
+ <field name="name">NAMSD</field>
+ <field name="long_name">neuropathy, axonal, motor-sensory with deafness and mental retardation (Cowchock syndrome)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24-q26.1</field>
+ <field name="info">
+Cowchock syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NAPB">
+ <field name="name">NAPB</field>
+ <field name="long_name">N-ethylmaleimide-sensitive factor attachment protein, beta</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+Leukemia, acute myeloid, therapy-related
+Ovarian carcinoma
+Amyotrophy, hereditary neuralgic [MIM:162100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NAT1">
+ <field name="name">NAT1</field>
+ <field name="long_name">N-acetyltransferase 1 (arylamine N-acetyltransferase)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23.1-p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NAT2">
+ <field name="name">NAT2</field>
+ <field name="long_name">N-acetyltransferase 2 (arylamine N-acetyltransferase)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23.1-p21.3</field>
+ <field name="info">
+Acetylation, slow [MIM:243400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NAV2">
+ <field name="name">NAV2</field>
+ <field name="long_name">neuron navigator 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NA">
+ <field name="name">NA</field>
+ <field name="long_name">neurocanthocytosis</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NBEA">
+ <field name="name">NBEA</field>
+ <field name="long_name">neurobeachin</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NCALD">
+ <field name="name">NCALD</field>
+ <field name="long_name">neurocalcin delta</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q22.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NCAM1">
+ <field name="name">NCAM1</field>
+ <field name="long_name">neural cell adhesion molecule 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NCF1">
+ <field name="name">NCF1</field>
+ <field name="long_name">neutrophil cytosolic factor 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.23</field>
+ <field name="info">
+Chronic granulomatous disease due to deficiency of NCF-1 [MIM:233700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NCF2">
+ <field name="name">NCF2</field>
+ <field name="long_name">neutrophil cytosolic factor 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q25</field>
+ <field name="info">
+Chronic granulomatous disease due to deficiency of NCF-2 [MIM:233710]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NCL">
+ <field name="name">NCL</field>
+ <field name="long_name">nucleolin</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q12-qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NCOA3">
+ <field name="name">NCOA3</field>
+ <field name="long_name">nuclear receptor coactivator 3</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NCOA4">
+ <field name="name">NCOA4</field>
+ <field name="long_name">nuclear receptor coactivator 4</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q11.2</field>
+ <field name="info">
+Thyroid carcinoma, papillary [MIM:188550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NCR3">
+ <field name="name">NCR3</field>
+ <field name="long_name">natural cytotoxicity triggering receptor 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Malaria, mild, susceptibility to [MIM:609148]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDIC">
+ <field name="name">NDIC</field>
+ <field name="long_name">Nail dysplasia, isolated congenital</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13</field>
+ <field name="info">
+Nail dysplasia, isolated congenital</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDN">
+ <field name="name">NDN</field>
+ <field name="long_name">necdin homolog (mouse)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q11-q13</field>
+ <field name="info">
+Prader-Willi syndrome [MIM:176270]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDP">
+ <field name="name">NDP</field>
+ <field name="long_name">Norrie disease (pseudoglioma)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.4</field>
+ <field name="info">
+Norrie disease [MIM:310600]
+Exudative vitreoretinopathy, X-linked [MIM:305390]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDRG1">
+ <field name="name">NDRG1</field>
+ <field name="long_name">N-myc downstream regulated 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.3</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 4D [MIM:601455]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFA11">
+ <field name="name">NDUFA11</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 11, 14.7kDa</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Mitochondrial complex I deficiency [MIM:252010]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFA12">
+ <field name="name">NDUFA12</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 12</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q12.1</field>
+ <field name="info">
+Mitochondrial complex I deficiency [MIM:252010]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFA13">
+ <field name="name">NDUFA13</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2-p13.1</field>
+ <field name="info">
+Thyroid carcinoma, Hurthle cell [MIM:607464]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFA1">
+ <field name="name">NDUFA1</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 1, 7.5kDa</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24</field>
+ <field name="info">
+Mitochondrial complex I deficiency [MIM:252010]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFA2">
+ <field name="name">NDUFA2</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 2, 8kDa</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.2</field>
+ <field name="info">
+Leigh syndrome due to mitochondrial complex I deficiency [MIM:256000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFAF1">
+ <field name="name">NDUFAF1</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFS1">
+ <field name="name">NDUFS1</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) Fe-S protein 1, 75kDa (NADH-coenzyme Q reductase)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33-q34</field>
+ <field name="info">
+Mitochondrial complex I deficiency [MIM:252010]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFS2">
+ <field name="name">NDUFS2</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) Fe-S protein 2, 49kDa (NADH-coenzyme Q reductase)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23</field>
+ <field name="info">
+Mitochondrial complex I deficiency [MIM:252010]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFS3">
+ <field name="name">NDUFS3</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) Fe-S protein 3, 30kDa (NADH-coenzyme Q reductase)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p11.11</field>
+ <field name="info">
+Leigh syndrome [MIM:256000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFS4">
+ <field name="name">NDUFS4</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q11.1</field>
+ <field name="info">
+Leigh syndrome [MIM:256000]
+Mitochondrial complex I deficiency [MIM:252010]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFS6">
+ <field name="name">NDUFS6</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) Fe-S protein 6, 13kDa (NADH-coenzyme Q reductase)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5pter-p15.33</field>
+ <field name="info">
+Complex I, mitochondrial respiratory chain, deficiency of [MIM:252010]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFS7">
+ <field name="name">NDUFS7</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13</field>
+ <field name="info">
+Leigh syndrome [MIM:256000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFS8">
+ <field name="name">NDUFS8</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) Fe-S protein 8, 23kDa (NADH-coenzyme Q reductase)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Leigh syndrome [MIM:256000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFV1">
+ <field name="name">NDUFV1</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) flavoprotein 1, 51kDa</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Leigh syndrome [MIM:256000]
+Alexander disease [MIM:203450]
+Mitochondrial complex I deficiency [MIM:252010]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NDUFV2">
+ <field name="name">NDUFV2</field>
+ <field name="long_name">NADH dehydrogenase (ubiquinone) flavoprotein 2, 24kDa</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.31-p11.2</field>
+ <field name="info">
+Parkinson disease, susceptibility to [MIM:168600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NEB">
+ <field name="name">NEB</field>
+ <field name="long_name">nebulin</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q22</field>
+ <field name="info">
+Nemaline myopathy 2, autosomal recessive [MIM:256030]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NEDD4L">
+ <field name="name">NEDD4L</field>
+ <field name="long_name">neural precursor cell expressed, developmentally down-regulated 4-like</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NEDE">
+ <field name="name">NEDE</field>
+ <field name="long_name">nephropathy, progressive, with deafness</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q24</field>
+ <field name="info">
+Nephropathy, progressive, with deafness</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NEFH">
+ <field name="name">NEFH</field>
+ <field name="long_name">neurofilament, heavy polypeptide</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.2</field>
+ <field name="info">
+Amyotrophic lateral sclerosis, susceptibility to [MIM:105400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NEFL">
+ <field name="name">NEFL</field>
+ <field name="long_name">neurofilament, light polypeptide</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 2E [MIM:607684]
+Charcot-Marie-Tooth disease, type 1F [MIM:607734]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NEFM">
+ <field name="name">NEFM</field>
+ <field name="long_name">neurofilament, medium polypeptide</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NEK8">
+ <field name="name">NEK8</field>
+ <field name="long_name">NIMA (never in mitosis gene a)- related kinase 8</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.1</field>
+ <field name="info">
+Nephronophthisis 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NELF">
+ <field name="name">NELF</field>
+ <field name="long_name">nasal embryonic LHRH factor</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.3</field>
+ <field name="info">
+Hypogonadotropic hypogonadism [MIM:146110]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NELL1">
+ <field name="name">NELL1</field>
+ <field name="long_name">NEL-like 1 (chicken)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.2-p15.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NET1">
+ <field name="name">NET1</field>
+ <field name="long_name">neuroepithelial cell transforming 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q12.2</field>
+ <field name="info">
+Orthostatic intolerance [MIM:604715]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NEU1">
+ <field name="name">NEU1</field>
+ <field name="long_name">sialidase 1 (lysosomal sialidase)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Sialidosis, type I [MIM:256550]
+Sialidosis, type II [MIM:256550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NEU2">
+ <field name="name">NEU2</field>
+ <field name="long_name">sialidase 2 (cytosolic sialidase)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NEUROD1">
+ <field name="name">NEUROD1</field>
+ <field name="long_name">neurogenic differentiation 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q32</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NEUROG3">
+ <field name="name">NEUROG3</field>
+ <field name="long_name">neurogenin 3</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21.3</field>
+ <field name="info">
+Diarrhea 4, malabsorptive, congenital [MIM:610370]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NF1">
+ <field name="name">NF1</field>
+ <field name="long_name">neurofibromin 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2</field>
+ <field name="info">
+Neurofibromatosis, type 1
+Watson syndrome [MIM:193520]
+Leukemia, juvenile myelomonocytic [MIM:607785]
+Melanoma, desmoplastic neurotropic
+Neurofibromatosis, familial spinal [MIM:162210]
+Neurofibromatosis-Noonan syndrome [MIM:601321]
+Pseudarthrosis, tibial, in NF1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NF2">
+ <field name="name">NF2</field>
+ <field name="long_name">neurofibromin 2 (merlin)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.2</field>
+ <field name="info">
+Neurofibromatosis, type 2 [MIM:101000]
+Meningioma, NF2-related, somatic [MIM:607174]
+Schwannomatosis [MIM:162091]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NFATC4">
+ <field name="name">NFATC4</field>
+ <field name="long_name">nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 4</field>
+ <field name="chromosome">14</field>
+ <field name="location">14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NFE2L2">
+ <field name="name">NFE2L2</field>
+ <field name="long_name">nuclear factor (erythroid-derived 2)-like 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NFIA">
+ <field name="name">NFIA</field>
+ <field name="long_name">nuclear factor I/A</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31.3-p31.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NFKB1">
+ <field name="name">NFKB1</field>
+ <field name="long_name">nuclear factor of kappa light polypeptide gene enhancer in B-cells 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q23-q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NFKB2">
+ <field name="name">NFKB2</field>
+ <field name="long_name">nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+lymphoma,B cell,non Hodgkin,associated with breakpoint in t(10;14)(q24;q32) translocation</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NFKBIA">
+ <field name="name">NFKBIA</field>
+ <field name="long_name">nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q13</field>
+ <field name="info">
+Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency [MIM:612132]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NFKBIL1">
+ <field name="name">NFKBIL1</field>
+ <field name="long_name">nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor-like 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Rheumatoid arthritis, susceptibility to [MIM:180300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NGFR">
+ <field name="name">NGFR</field>
+ <field name="long_name">nerve growth factor receptor (TNFR superfamily, member 16)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NGF">
+ <field name="name">NGF</field>
+ <field name="long_name">nerve growth factor (beta polypeptide)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NHEJ1">
+ <field name="name">NHEJ1</field>
+ <field name="long_name">nonhomologous end-joining factor 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35</field>
+ <field name="info">
+Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation [MIM:611291]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NHLRC1">
+ <field name="name">NHLRC1</field>
+ <field name="long_name">NHL repeat containing 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p22.3</field>
+ <field name="info">
+Epilepsy, myoclonic, Lafora type [MIM:254780]
+Epilepsy, progressive myoclonic 2B [MIM:254780]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NHS">
+ <field name="name">NHS</field>
+ <field name="long_name">Nance-Horan syndrome (congenital cataracts and dental anomalies)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.13</field>
+ <field name="info">
+Nance-Horan syndrome [MIM:302350]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NIDDM1">
+ <field name="name">NIDDM1</field>
+ <field name="long_name">non-insulin-dependent diabetes mellitus (common, type 2) 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.3</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent 1 [MIM:601283]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NIDDM2">
+ <field name="name">NIDDM2</field>
+ <field name="long_name">non-insulin-dependent diabetes mellitus (common, type 2) 2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.2</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NIDDM3">
+ <field name="name">NIDDM3</field>
+ <field name="long_name">Noninsulin-dependent diabetes mellitus 3</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q12-q13.1</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NIDDM4">
+ <field name="name">NIDDM4</field>
+ <field name="long_name">Diabetes mellitus, noninsulin-dependent</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q34-q35.2</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NINJ1">
+ <field name="name">NINJ1</field>
+ <field name="long_name">ninjurin 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NIPA1">
+ <field name="name">NIPA1</field>
+ <field name="long_name">non imprinted in Prader-Willi/Angelman syndrome 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q11.1</field>
+ <field name="info">
+Spastic paraplegia-6 [MIM:600363]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NIPBL">
+ <field name="name">NIPBL</field>
+ <field name="long_name">Nipped-B homolog (Drosophila)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13.1</field>
+ <field name="info">
+Cornelia de Lange syndrome 1 [MIM:122470]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NKAIN2">
+ <field name="name">NKAIN2</field>
+ <field name="long_name">Na+/K+ transporting ATPase interacting 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+Developmental delay and recurrent infections</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NKCD">
+ <field name="name">NKCD</field>
+ <field name="long_name">Natural killer cell deficiency, familial isolated</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p11.23-q11.21</field>
+ <field name="info">
+Natural killer cell deficiency, familial isolated</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NKX2-1">
+ <field name="name">NKX2-1</field>
+ <field name="long_name">NK2 homeobox 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q13</field>
+ <field name="info">
+Goiter, familial, due to TTF-1 defect
+Chorea, hereditary benign [MIM:118700]
+Choreoathetosis, hypothyroidism, and neonatal respiratory distress [MIM:610978]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NKX2-6">
+ <field name="name">NKX2-6</field>
+ <field name="long_name">NK2 transcription factor related, locus 6 (Drosophila)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21</field>
+ <field name="info">
+Persistent truncus arteriosus [MIM:217095]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NLGN3">
+ <field name="name">NLGN3</field>
+ <field name="long_name">neuroligin 3</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13</field>
+ <field name="info">
+Autism, susceptibility to, X-linked-1 [MIM:300425]
+Asperger syndrome, susceptibility to, X-linked-1 [MIM:300494]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NLGN4Y">
+ <field name="name">NLGN4Y</field>
+ <field name="long_name">neuroligin 4, Y-linked</field>
+ <field name="chromosome">Y</field>
+ <field name="location">Yq11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NMB">
+ <field name="name">NMB</field>
+ <field name="long_name">neuromedin B</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22-qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NME1">
+ <field name="name">NME1</field>
+ <field name="long_name">non-metastatic cells 1, protein (NM23A) expressed in</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.3</field>
+ <field name="info">
+Neuroblastoma [MIM:256700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NMSR">
+ <field name="name">NMSR</field>
+ <field name="long_name">Neuropathy, hereditary motor and sensory, Russe type</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23.2</field>
+ <field name="info">
+Neuropathy, motor and sensory, Russe type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NMT2">
+ <field name="name">NMT2</field>
+ <field name="long_name">N-myristoyltransferase 2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NMTC1">
+ <field name="name">NMTC1</field>
+ <field name="long_name">Nonmedullary thyroid carcinoma 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q21</field>
+ <field name="info">
+Thyroid carcinoma, nonmedullary, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NM">
+ <field name="name">NM</field>
+ <field name="long_name">neutrophil migration</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22-qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NNMT">
+ <field name="name">NNMT</field>
+ <field name="long_name">nicotinamide N-methyltransferase</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.1</field>
+ <field name="info">
+Homocysteine plasma level</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NNO1">
+ <field name="name">NNO1</field>
+ <field name="long_name">nanophthalmos 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p</field>
+ <field name="info">
+Nanophthalmos-1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NNO3">
+ <field name="name">NNO3</field>
+ <field name="long_name">nanophthalmos 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q11-q14</field>
+ <field name="info">
+Nanophthalmos 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NOBOX">
+ <field name="name">NOBOX</field>
+ <field name="long_name">NOBOX oogenesis homeobox</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q35</field>
+ <field name="info">
+Premature ovarian failure 5 [MIM:611548]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NOD1">
+ <field name="name">NOD1</field>
+ <field name="long_name">nucleotide-binding oligomerization domain containing 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15-p14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NOD2">
+ <field name="name">NOD2</field>
+ <field name="long_name">nucleotide-binding oligomerization domain containing 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q12</field>
+ <field name="info">
+Crohn disease, susceptibility to [MIM:266600]
+Blau syndrome [MIM:186580]
+Psoriatic arthritis, susceptibility to [MIM:607507]
+Sarcoidosis, early-onset [MIM:609464]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NODAL">
+ <field name="name">NODAL</field>
+ <field name="long_name">nodal homolog (mouse)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10</field>
+ <field name="info">
+Situs ambiguus</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NOG">
+ <field name="name">NOG</field>
+ <field name="long_name">noggin</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q22</field>
+ <field name="info">
+Symphalangism, proximal [MIM:185800]
+Synostoses syndrome, multiple, 1 [MIM:186500]
+Tarsal-carpal coalition syndrome [MIM:186570]
+Stapes ankylosis with broad thumb and toes [MIM:184460]
+Brachydactyly, type B2 [MIM:611377]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NOP10">
+ <field name="name">NOP10</field>
+ <field name="long_name">NOP10 ribonucleoprotein homolog (yeast)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q14-q15</field>
+ <field name="info">
+Dyskeratosis congenita, autosomal recessive [MIM:224230]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NOS1AP">
+ <field name="name">NOS1AP</field>
+ <field name="long_name">nitric oxide synthase 1 (neuronal) adaptor protein</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23.3</field>
+ <field name="info">
+QT interval, modifier of [MIM:610141]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NOS1">
+ <field name="name">NOS1</field>
+ <field name="long_name">nitric oxide synthase 1 (neuronal)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.2-q24.31</field>
+ <field name="info">
+Pyloric stenosis, infantile hypertrophic, 1, susceptibility to [MIM:179010]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NOS2">
+ <field name="name">NOS2</field>
+ <field name="long_name">nitric oxide synthase 2, inducible</field>
+ <field name="chromosome">17</field>
+ <field name="location">17cen-q11.2</field>
+ <field name="info">
+Hypertension, susceptibility to [MIM:145500]
+Malaria, resistance to [MIM:611162]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NOS3">
+ <field name="name">NOS3</field>
+ <field name="long_name">nitric oxide synthase 3 (endothelial cell)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q36</field>
+ <field name="info">
+Coronary spasms, susceptibility to
+Alzheimer disease, late-onset, susceptibility to [MIM:104300]
+Hypertension, susceptibility to [MIM:145500]
+Hypertension, pregnancy-induced [MIM:189800]
+Placental abruption
+Ischemic stroke, susceptibility to [MIM:601367]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NOTCH1">
+ <field name="name">NOTCH1</field>
+ <field name="long_name">Notch homolog 1, translocation-associated (Drosophila)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.3</field>
+ <field name="info">
+Aortic valve disease [MIM:109730]
+Leukemia, T-cell acute lymphoblastic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NOTCH2">
+ <field name="name">NOTCH2</field>
+ <field name="long_name">Notch homolog 2 (Drosophila)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13-p11</field>
+ <field name="info">
+Alagille syndrome 2 [MIM:610205]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NOTCH3">
+ <field name="name">NOTCH3</field>
+ <field name="long_name">Notch homolog 3 (Drosophila)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2-p13.1</field>
+ <field name="info">
+Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy [MIM:125310]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NOTCH4">
+ <field name="name">NOTCH4</field>
+ <field name="long_name">Notch homolog 4 (Drosophila)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPAS2">
+ <field name="name">NPAS2</field>
+ <field name="long_name">neuronal PAS domain protein 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPAS3">
+ <field name="name">NPAS3</field>
+ <field name="long_name">neuronal PAS domain protein 3</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPC1L1">
+ <field name="name">NPC1L1</field>
+ <field name="long_name">NPC1 (Niemann-Pick disease, type C1, gene)-like 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p13</field>
+ <field name="info">
+Ezetimibe, nonresponse to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPC1">
+ <field name="name">NPC1</field>
+ <field name="long_name">Niemann-Pick disease, type C1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15.1-q12</field>
+ <field name="info">
+Nasopharyngeal carcinoma 1 [MIM:161550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPC2">
+ <field name="name">NPC2</field>
+ <field name="long_name">Niemann-Pick disease, type C2</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3</field>
+ <field name="info">
+Niemann-pick disease, type C2 [MIM:607625]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPHL1">
+ <field name="name">NPHL1</field>
+ <field name="long_name">nephrolithiasis 1 (X-linked)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.22</field>
+ <field name="info">
+Dent disease [MIM:300009]
+Nephrolithiasis, type I [MIM:310468]
+Hypophosphatemic rickets [MIM:300554]
+Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis [MIM:308990]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPHP1">
+ <field name="name">NPHP1</field>
+ <field name="long_name">nephronophthisis 1 (juvenile)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q13</field>
+ <field name="info">
+Nephronophthisis, juvenile [MIM:256100]
+Senior-Loken syndrome-1 [MIM:266900]
+Joubert syndrome 4 [MIM:609583]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPHP3">
+ <field name="name">NPHP3</field>
+ <field name="long_name">nephronophthisis 3 (adolescent)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q22</field>
+ <field name="info">
+Nephronophthisis, adolescent [MIM:604387]
+Renal-hepatic-pancreatic dysplasia with Dandy-Walker cyst [MIM:208540]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPHP4">
+ <field name="name">NPHP4</field>
+ <field name="long_name">nephronophthisis 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Nephronophthisis 4 [MIM:606966]
+Senior-Loken syndrome 4 [MIM:606996]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPHS1">
+ <field name="name">NPHS1</field>
+ <field name="long_name">nephrosis 1, congenital, Finnish type (nephrin)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+Nephrosis-1, congenital, Finnish type [MIM:256300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPHS2">
+ <field name="name">NPHS2</field>
+ <field name="long_name">nephrosis 2, idiopathic, steroid-resistant (podocin)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q25-q31</field>
+ <field name="info">
+Nephrotic syndrome, steroid-resistant, autosomal recessive [MIM:600995]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPM1">
+ <field name="name">NPM1</field>
+ <field name="long_name">nucleophosmin (nucleolar phosphoprotein B23, numatrin)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q35</field>
+ <field name="info">
+Leukemia, acute promyelocytic, NPM/RARA type
+Leukemia, acute myeloid [MIM:601626]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPPA">
+ <field name="name">NPPA</field>
+ <field name="long_name">natriuretic peptide precursor A</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2</field>
+ <field name="info">
+Atrial fibrillation, familial, 6 [MIM:612201]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPPB">
+ <field name="name">NPPB</field>
+ <field name="long_name">natriuretic peptide precursor B</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPPC">
+ <field name="name">NPPC</field>
+ <field name="long_name">natriuretic peptide precursor C</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q24-qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPR1">
+ <field name="name">NPR1</field>
+ <field name="long_name">natriuretic peptide receptor A/guanylate cyclase A (atrionatriuretic peptide receptor A)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPR2">
+ <field name="name">NPR2</field>
+ <field name="long_name">natriuretic peptide receptor B/guanylate cyclase B (atrionatriuretic peptide receptor B)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21-p12</field>
+ <field name="info">
+Acromesomelic dysplasia, Maroteaux type [MIM:602875]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPR3">
+ <field name="name">NPR3</field>
+ <field name="long_name">natriuretic peptide receptor C/guanylate cyclase C (atrionatriuretic peptide receptor C)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p14-p12</field>
+ <field name="info">
+Hypertension, salt-resistant</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPSR1">
+ <field name="name">NPSR1</field>
+ <field name="long_name">neuropeptide S receptor 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15-p14</field>
+ <field name="info">
+Asthma, susceptibility to, 2 [MIM:608584]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPY2R">
+ <field name="name">NPY2R</field>
+ <field name="long_name">neuropeptide Y receptor Y2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NPY">
+ <field name="name">NPY</field>
+ <field name="long_name">neuropeptide Y</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NP">
+ <field name="name">NP</field>
+ <field name="long_name">nucleoside phosphorylase</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q13.1</field>
+ <field name="info">
+Nucleoside phosphorylase deficiency, immunodeficiency due to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NQO1">
+ <field name="name">NQO1</field>
+ <field name="long_name">NAD(P)H dehydrogenase, quinone 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22.1</field>
+ <field name="info">
+Benzene toxicity, susceptibility to
+Leukemia, post-chemotherapy, susceptibility to
+Breast cancer, poor survival after chemotherapy for (3) 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NQO2">
+ <field name="name">NQO2</field>
+ <field name="long_name">NAD(P)H dehydrogenase, quinone 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p25</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NR0B2">
+ <field name="name">NR0B2</field>
+ <field name="long_name">nuclear receptor subfamily 0, group B, member 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.1</field>
+ <field name="info">
+Obesity, mild, early-onset [MIM:601665]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NR1I2">
+ <field name="name">NR1I2</field>
+ <field name="long_name">nuclear receptor subfamily 1, group I, member 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q13-q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NR2E1">
+ <field name="name">NR2E1</field>
+ <field name="long_name">nuclear receptor subfamily 2, group E, member 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NR2E3">
+ <field name="name">NR2E3</field>
+ <field name="long_name">nuclear receptor subfamily 2, group E, member 3</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q23</field>
+ <field name="info">
+Enhanced S-cone syndrome [MIM:268100]
+Retinitis pigmentosa-37 [MIM:611131]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NR3C1">
+ <field name="name">NR3C1</field>
+ <field name="long_name">nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Cortisol resistance</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NR3C2">
+ <field name="name">NR3C2</field>
+ <field name="long_name">nuclear receptor subfamily 3, group C, member 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q31.1</field>
+ <field name="info">
+Pseudohypoaldosteronism type I, autosomal dominant [MIM:177735]
+Hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy [MIM:605115]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NR4A2">
+ <field name="name">NR4A2</field>
+ <field name="long_name">nuclear receptor subfamily 4, group A, member 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q22-q23</field>
+ <field name="info">
+Parkinson disease [MIM:168600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NR4A3">
+ <field name="name">NR4A3</field>
+ <field name="long_name">nuclear receptor subfamily 4, group A, member 3</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q11-q12</field>
+ <field name="info">
+Chondrosarcoma, extraskeletal myxoid [MIM:612237]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NRAS">
+ <field name="name">NRAS</field>
+ <field name="long_name">neuroblastoma RAS viral (v-ras) oncogene homolog</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13.2</field>
+ <field name="info">
+Colorectal cancer [MIM:114500]
+Thyroid carcinoma, follicular [MIM:188470]
+Autoimmune lymphoproliferative syndrome type IV</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NRCLP3">
+ <field name="name">NRCLP3</field>
+ <field name="long_name">Narcolepsy 3</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q11.2</field>
+ <field name="info">
+Narcolepsy 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NRCLP4">
+ <field name="name">NRCLP4</field>
+ <field name="long_name">Narcolepsy 4</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13</field>
+ <field name="info">
+Narcolepsy 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NRG1">
+ <field name="name">NRG1</field>
+ <field name="long_name">neuregulin 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p22-p11</field>
+ <field name="info">
+Schizophrenia, susceptibility to [MIM:603013]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NRIP1">
+ <field name="name">NRIP1</field>
+ <field name="long_name">nuclear receptor interacting protein 1</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NRL">
+ <field name="name">NRL</field>
+ <field name="long_name">neural retina leucine zipper</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.1-q11.2</field>
+ <field name="info">
+Retinitis pigmentosa-27
+Retinal degeneration, autosomal recessive, clumped pigment type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NRP2">
+ <field name="name">NRP2</field>
+ <field name="long_name">neuropilin 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q34</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NRTN">
+ <field name="name">NRTN</field>
+ <field name="long_name">neurturin</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Hirschsprung Disease</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NRXN1">
+ <field name="name">NRXN1</field>
+ <field name="long_name">neurexin 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p16.3</field>
+ <field name="info">
+Autism, susceptibility to [MIM:209850]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NRXN3">
+ <field name="name">NRXN3</field>
+ <field name="long_name">neurexin 3</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3-q31.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NSD1">
+ <field name="name">NSD1</field>
+ <field name="long_name">nuclear receptor binding SET domain protein 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q35</field>
+ <field name="info">
+Sotos syndrome [MIM:117550]
+Leukemia, acute myeloid [MIM:601626]
+Weaver syndrome [MIM:277590]
+Beckwith-Wiedemann syndrome [MIM:130650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NSDHL">
+ <field name="name">NSDHL</field>
+ <field name="long_name">NAD(P) dependent steroid dehydrogenase-like</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+CHILD syndrome [MIM:308050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NSF">
+ <field name="name">NSF</field>
+ <field name="long_name">N-ethylmaleimide-sensitive factor</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NT5C3">
+ <field name="name">NT5C3</field>
+ <field name="long_name">5'-nucleotidase, cytosolic III</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15-p14</field>
+ <field name="info">
+Anemia, hemolytic, due to UMPH1 deficiency [MIM:266120]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NTF3">
+ <field name="name">NTF3</field>
+ <field name="long_name">neurotrophin 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NTNG1">
+ <field name="name">NTNG1</field>
+ <field name="long_name">netrin G1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NTRK1">
+ <field name="name">NTRK1</field>
+ <field name="long_name">neurotrophic tyrosine kinase, receptor, type 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21-q22</field>
+ <field name="info">
+Insensitivity to pain, congenital, with anhidrosis [MIM:256800]
+Medullary thyroid carcinoma, familial [MIM:155240]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NTRK2">
+ <field name="name">NTRK2</field>
+ <field name="long_name">neurotrophic tyrosine kinase, receptor, type 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22.1</field>
+ <field name="info">
+Obesity, hyperphagia, and developmental delay</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NTS">
+ <field name="name">NTS</field>
+ <field name="long_name">neurotensin</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NUDT1">
+ <field name="name">NUDT1</field>
+ <field name="long_name">nudix (nucleoside diphosphate linked moiety X)-type motif 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NUMA1">
+ <field name="name">NUMA1</field>
+ <field name="long_name">nuclear mitotic apparatus protein 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Leukemia, acute promyelocytic, NUMA/RARA type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NUMBL">
+ <field name="name">NUMBL</field>
+ <field name="long_name">numb homolog (Drosophila)-like</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.13-q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NUMB">
+ <field name="name">NUMB</field>
+ <field name="long_name">numb homolog (Drosophila)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NUP155">
+ <field name="name">NUP155</field>
+ <field name="long_name">nucleoporin 155kDa</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NUP214">
+ <field name="name">NUP214</field>
+ <field name="long_name">nucleoporin 214kDa</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.1</field>
+ <field name="info">
+Leukemia, acute myeloid [MIM:601626]
+Leukemia, T-cell acute lymphoblastic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NUP62">
+ <field name="name">NUP62</field>
+ <field name="long_name">nucleoporin 62kDa</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.33</field>
+ <field name="info">
+Striatonigral degeneration, infantile [MIM:271930]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NUP98">
+ <field name="name">NUP98</field>
+ <field name="long_name">nucleoporin 98kDa</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15</field>
+ <field name="info">
+Leukemia, lymphycytic, acute T-cell</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NXF5">
+ <field name="name">NXF5</field>
+ <field name="long_name">nuclear RNA export factor 5</field>
+ <field name="chromosome">X</field>
+ <field name="location">X</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="NYS2">
+ <field name="name">NYS2</field>
+ <field name="long_name">nystagmus 2, congenital autosomal dominant</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12</field>
+ <field name="info">
+Nystagmus-2, autosomal dominant</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NYS3">
+ <field name="name">NYS3</field>
+ <field name="long_name">nystagmus 3, congenital autosomal dominant</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p11.2</field>
+ <field name="info">
+Nystagmus 3, congenital</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NYS4">
+ <field name="name">NYS4</field>
+ <field name="long_name">nystagmus 4, congenital autosomal dominant</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q31-q33</field>
+ <field name="info">
+Nystagmus 4, congenital</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NYS5">
+ <field name="name">NYS5</field>
+ <field name="long_name">Nystagmus 5, infantile periodic alternating</field>
+ <field name="chromosome">X</field>
+ <field name="location">X</field>
+ <field name="info">
+Nystagmus 5, infantile periodic alternating</field>
+</record>
+<record model="gnuhealth.disease.gene" id="NYX">
+ <field name="name">NYX</field>
+ <field name="long_name">nyctalopin</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.4</field>
+ <field name="info">
+Night blindness, congenital stationary, type 1 [MIM:310500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OA1">
+ <field name="name">OA1</field>
+ <field name="long_name">Osteoarthritis QTL 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3</field>
+ <field name="info">
+Ocular albinism with sensorineural deafness</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OA2">
+ <field name="name">OA2</field>
+ <field name="long_name">Osteoarthritis QTL 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23</field>
+ <field name="info">
+Night blindness, congenital stationary, X-linked, type 2A [MIM:300071]
+Cone-rod dystrophy, X-linked, 3 [MIM:300476]
+Aland Island eye disease [MIM:300600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OADIP">
+ <field name="name">OADIP</field>
+ <field name="long_name">Osteoarthritis of distal interphalangeal joints</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q12-q13</field>
+ <field name="info">
+Osteoarthritis of distal interphalangeal joints</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OAS1">
+ <field name="name">OAS1</field>
+ <field name="long_name">2',5'-oligoadenylate synthetase 1, 40/46kDa</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.2</field>
+ <field name="info">
+Viral infection, susceptibility to
+Diabetes mellitus, type 1, susceptibility to [MIM:222100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OAS2">
+ <field name="name">OAS2</field>
+ <field name="long_name">2'-5'-oligoadenylate synthetase 2, 69/71kDa</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="OASD">
+ <field name="name">OASD</field>
+ <field name="long_name">ocular albinism and sensorineural deafness</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3</field>
+ <field name="info">
+Ocular albinism with sensorineural deafness</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OAT">
+ <field name="name">OAT</field>
+ <field name="long_name">ornithine aminotransferase (gyrate atrophy)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q26</field>
+ <field name="info">
+Gyrate atrophy of choroid and retina with ornithinemia, B6 responsive or unresponsive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OAZ1">
+ <field name="name">OAZ1</field>
+ <field name="long_name">ornithine decarboxylase antizyme 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="OCA2">
+ <field name="name">OCA2</field>
+ <field name="long_name">oculocutaneous albinism II</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q11.2-q12</field>
+ <field name="info">
+Albinism, oculocutaneous, type II [MIM:203200]
+Albinism, brown oculocutaneous [MIM:203200]
+Skin/hair/eye pigmentation 1, blue/nonblue eyes [MIM:227220]
+Skin/hair/eye pigmentation 1, blond/brown hair [MIM:227220]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OCD1">
+ <field name="name">OCD1</field>
+ <field name="long_name">obsessive-compulsive disorder 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.1-q12</field>
+ <field name="info">
+Anxiety-related personality traits [MIM:607834]
+Obsessive-compulsive disorder 1 [MIM:164230]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OCRL">
+ <field name="name">OCRL</field>
+ <field name="long_name">oculocerebrorenal syndrome of Lowe</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26.1</field>
+ <field name="info">
+Lowe syndrome [MIM:309000]
+Dent disease 2 [MIM:300555]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ODC1">
+ <field name="name">ODC1</field>
+ <field name="long_name">ornithine decarboxylase 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p25</field>
+ <field name="info">
+Colonic adenoma recurrence, reduced risk of [MIM:114500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ODCP">
+ <field name="name">ODCP</field>
+ <field name="long_name">ornithine decarboxylase pseudogene</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p25</field>
+ <field name="info">
+Colonic adenoma recurrence, reduced risk of [MIM:114500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ODPF">
+ <field name="name">ODPF</field>
+ <field name="long_name">Osseous dysplasia, digital, with facial pigmentary defects and multiple frenula</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq27.3-q28</field>
+ <field name="info">
+Osseous dysplasia, digital, with facial pigmentary defects and multiple frenula</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ODS1">
+ <field name="name">ODS1</field>
+ <field name="long_name">Opioid dependence, susceptibility to, 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17</field>
+ <field name="info">
+Opioid dependence, susceptibility to, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OFC1">
+ <field name="name">OFC1</field>
+ <field name="long_name">orofacial cleft 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p24.3</field>
+ <field name="info">
+Orofacial cleft-1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OFC2">
+ <field name="name">OFC2</field>
+ <field name="long_name">orofacial cleft 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p13</field>
+ <field name="info">
+Orofacial cleft-2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OFC3">
+ <field name="name">OFC3</field>
+ <field name="long_name">orofacial cleft 3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+Orofacial cleft-3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OFC4">
+ <field name="name">OFC4</field>
+ <field name="long_name">Orofacial cleft 4</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21-q31</field>
+ <field name="info">
+Orofacial cleft 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OFD1">
+ <field name="name">OFD1</field>
+ <field name="long_name">oral-facial-digital syndrome 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3-p22.2</field>
+ <field name="info">
+Oral-facial-digital syndrome 1 [MIM:311200]
+Simpson-Golabi-Behmel syndrome, type 2 [MIM:300209]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OGDH">
+ <field name="name">OGDH</field>
+ <field name="long_name">oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14-p13</field>
+ <field name="info">
+Alpha-ketoglutarate dehydrogenase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OGG1">
+ <field name="name">OGG1</field>
+ <field name="long_name">8-oxoguanine DNA glycosylase</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26.2</field>
+ <field name="info">
+Renal cell carcinoma, clear cell, somatic [MIM:144700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OGS2">
+ <field name="name">OGS2</field>
+ <field name="long_name">Opitz G syndrome, type II</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+Opitz G syndrome, type II</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OHDS">
+ <field name="name">OHDS</field>
+ <field name="long_name">Orthostatic hypotensive disorder of Streeten</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q</field>
+ <field name="info">
+Orthostatic hypotensive disorder of Streeten</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OLR1">
+ <field name="name">OLR1</field>
+ <field name="long_name">oxidized low density lipoprotein (lectin-like) receptor 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13-p12</field>
+ <field name="info">
+Myocardial infarction, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OMG">
+ <field name="name">OMG</field>
+ <field name="long_name">oligodendrocyte myelin glycoprotein</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="OMP">
+ <field name="name">OMP</field>
+ <field name="long_name">olfactory marker protein</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.4-q14.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="OMS">
+ <field name="name">OMS</field>
+ <field name="long_name">otitis media, susceptibility to</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q26.3</field>
+ <field name="info">
+Otitis media, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPA1">
+ <field name="name">OPA1</field>
+ <field name="long_name">optic atrophy 1 (autosomal dominant)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q28-q29</field>
+ <field name="info">
+Optic atrophy 1 [MIM:165500]
+Glaucoma, normal tension, susceptibility to [MIM:606657]
+Optic atrophy and deafness [MIM:125250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPA2">
+ <field name="name">OPA2</field>
+ <field name="long_name">optic atrophy 2 (obscure)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.4-p11.21</field>
+ <field name="info">
+Optic atrophy, X-linked</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPA3">
+ <field name="name">OPA3</field>
+ <field name="long_name">optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2-q13.3</field>
+ <field name="info">
+3-methylglutaconic aciduria, type III [MIM:258501]
+Optic atrophy and cataract [MIM:165300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPA4">
+ <field name="name">OPA4</field>
+ <field name="long_name">optic atrophy 4 (autosomal dominant)</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q12.2-q12.3</field>
+ <field name="info">
+Optic atrophy-4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPA5">
+ <field name="name">OPA5</field>
+ <field name="long_name">optic atrophy 5 (autosomal dominant)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.1-q13.1</field>
+ <field name="info">
+Optic atrophy 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPA6">
+ <field name="name">OPA6</field>
+ <field name="long_name">optic atrophy 6 (autosomal recessive)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21-q22</field>
+ <field name="info">
+Optic atrophy 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPCML">
+ <field name="name">OPCML</field>
+ <field name="long_name">opioid binding protein/cell adhesion molecule-like</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q25</field>
+ <field name="info">
+Ovarian cancer, somatic [MIM:167000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPHN1">
+ <field name="name">OPHN1</field>
+ <field name="long_name">oligophrenin 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq12</field>
+ <field name="info">
+Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance [MIM:300486]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPLL">
+ <field name="name">OPLL</field>
+ <field name="long_name">ossification of posterior longitudinal ligament of spine</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Bethlem myopathy [MIM:158810]
+Ullrich congenital muscular dystrophy [MIM:254090]
+Ossification of the posterior longitudinal spinal ligaments [MIM:602475]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPN1LW">
+ <field name="name">OPN1LW</field>
+ <field name="long_name">opsin 1 (cone pigments), long-wave-sensitive</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Colorblindness, protan
+Blue-cone monochromacy [MIM:303700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPN1MW">
+ <field name="name">OPN1MW</field>
+ <field name="long_name">opsin 1 (cone pigments), medium-wave-sensitive</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Colorblindness, deutan
+Blue-cone monochromacy [MIM:303700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPN1SW">
+ <field name="name">OPN1SW</field>
+ <field name="long_name">opsin 1 (cone pigments), short-wave-sensitive</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31.3-q32</field>
+ <field name="info">
+Colorblindness, tritan</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPRK1">
+ <field name="name">OPRK1</field>
+ <field name="long_name">opioid receptor, kappa 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPRM1">
+ <field name="name">OPRM1</field>
+ <field name="long_name">opioid receptor, mu 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q24-q25</field>
+ <field name="info">
+Response to morphine-6-glucuronide
+Epilepsy, idiopathic generalized, susceptibility to [MIM:600669]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OPTN">
+ <field name="name">OPTN</field>
+ <field name="long_name">optineurin</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p15-p14</field>
+ <field name="info">
+Glaucoma 1, open angle, E [MIM:137760]
+Glaucoma, normal tension, susceptibility to [MIM:606657]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OR13G1">
+ <field name="name">OR13G1</field>
+ <field name="long_name">olfactory receptor, family 13, subfamily G, member 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q44</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="OR7D4">
+ <field name="name">OR7D4</field>
+ <field name="long_name">olfactory receptor, family 7, subfamily D, member 4</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ORW3">
+ <field name="name">ORW3</field>
+ <field name="long_name">Osler-Rendu-Weber syndrome 3</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.3-q32</field>
+ <field name="info">
+Osler-Rendu-Weber syndrome 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OS6">
+ <field name="name">OS6</field>
+ <field name="long_name">Osteoarthritis susceptibility 6</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p24.3</field>
+ <field name="info">
+Osteoarthritis susceptibility 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OSCS">
+ <field name="name">OSCS</field>
+ <field name="long_name">Osteopathia striata with cranial sclerosis</field>
+ <field name="chromosome">X</field>
+ <field name="location">X</field>
+ <field name="info">
+Osteopathia striata with cranial sclerosis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OSMR">
+ <field name="name">OSMR</field>
+ <field name="long_name">oncostatin M receptor</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13.1</field>
+ <field name="info">
+Amyloidosis, primary localized cutaneous [MIM:105250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OSTM1">
+ <field name="name">OSTM1</field>
+ <field name="long_name">osteopetrosis associated transmembrane protein 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+Osteopetrosis, autosomal recessive 5 [MIM:259720]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OTC">
+ <field name="name">OTC</field>
+ <field name="long_name">ornithine carbamoyltransferase</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp21.1</field>
+ <field name="info">
+Ornithine transcarbamylase deficiency [MIM:311250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OTOA">
+ <field name="name">OTOA</field>
+ <field name="long_name">otoancorin</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12.2</field>
+ <field name="info">
+Deafness, autosomal recessive 22 [MIM:607039]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OTOF">
+ <field name="name">OTOF</field>
+ <field name="long_name">otoferlin</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p23-p22</field>
+ <field name="info">
+Deafness, autosomal recessive 9 [MIM:601071]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OTOR">
+ <field name="name">OTOR</field>
+ <field name="long_name">otoraplin</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="OTSC1">
+ <field name="name">OTSC1</field>
+ <field name="long_name">otosclerosis 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26.1-qter</field>
+ <field name="info">
+Otosclerosis 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OTSC2">
+ <field name="name">OTSC2</field>
+ <field name="long_name">otosclerosis 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q34-q36</field>
+ <field name="info">
+Otosclerosis-2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OTSC3">
+ <field name="name">OTSC3</field>
+ <field name="long_name">otosclerosis 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p22.3-p21.3</field>
+ <field name="info">
+Otosclerosis 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OTSC4">
+ <field name="name">OTSC4</field>
+ <field name="long_name">otosclerosis 4</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22.1-q23.1</field>
+ <field name="info">
+Otosclerosis 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OTSC5">
+ <field name="name">OTSC5</field>
+ <field name="long_name">otosclerosis 5</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q22-q24</field>
+ <field name="info">
+Otosclerosis 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OTSC7">
+ <field name="name">OTSC7</field>
+ <field name="long_name">otosclerosis 7</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q13-q16.1</field>
+ <field name="info">
+Otosclerosis 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OTSC8">
+ <field name="name">OTSC8</field>
+ <field name="long_name">otosclerosis 8</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p13.1-q21.11</field>
+ <field name="info">
+Otsclerosis 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OTX2">
+ <field name="name">OTX2</field>
+ <field name="long_name">orthodenticle homeobox 2</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q21-q22</field>
+ <field name="info">
+Microphthalmia, syndromic 5 [MIM:610125]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OVCAS1">
+ <field name="name">OVCAS1</field>
+ <field name="long_name">Ovarian cancer, epithelial, susceptibility to</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25-p22</field>
+ <field name="info">
+Ovarian cancer, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="OXCT1">
+ <field name="name">OXCT1</field>
+ <field name="long_name">3-oxoacid CoA transferase 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13</field>
+ <field name="info">
+Succinyl CoA:3-oxoacid CoA transferase deficiency [MIM:245050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="P1">
+ <field name="name">P1</field>
+ <field name="long_name">P one antigen (P blood group)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2-qter</field>
+ <field name="info">
+Transcobalamin II deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="P2RX1">
+ <field name="name">P2RX1</field>
+ <field name="long_name">purinergic receptor P2X, ligand-gated ion channel, 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.3</field>
+ <field name="info">
+Bleeding disorder due to P2RX1 defect</field>
+</record>
+<record model="gnuhealth.disease.gene" id="P2RX7">
+ <field name="name">P2RX7</field>
+ <field name="long_name">purinergic receptor P2X, ligand-gated ion channel, 7</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="P2RY12">
+ <field name="name">P2RY12</field>
+ <field name="long_name">purinergic receptor P2Y, G-protein coupled, 12</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q24-q25</field>
+ <field name="info">
+Bleeding disorder due to P2RY12 defect [MIM:609821]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="P2RY5">
+ <field name="name">P2RY5</field>
+ <field name="long_name">purinergic receptor P2Y, G-protein coupled, 5</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14.12-q14.2</field>
+ <field name="info">
+Hypotrichosis, localized, autosomal recessive, 3 [MIM:611452]
+Woolly hair, autosomal recessive [MIM:278150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PABPN1">
+ <field name="name">PABPN1</field>
+ <field name="long_name">poly(A) binding protein, nuclear 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2-q13</field>
+ <field name="info">
+Oculopharyngeal muscular dystrophy [MIM:164300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PADI4">
+ <field name="name">PADI4</field>
+ <field name="long_name">peptidyl arginine deiminase, type IV</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.13</field>
+ <field name="info">
+Rheumatoid arthritis, susceptibility to [MIM:180300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAFAH1B1">
+ <field name="name">PAFAH1B1</field>
+ <field name="long_name">platelet-activating factor acetylhydrolase, isoform Ib, subunit 1 (45kDa)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.3</field>
+ <field name="info">
+Lissencephaly-1 [MIM:607432]
+Subcortical laminar heterotopia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAFAH1B3">
+ <field name="name">PAFAH1B3</field>
+ <field name="long_name">platelet-activating factor acetylhydrolase, isoform Ib, subunit 3 (29kDa)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAFC">
+ <field name="name">PAFC</field>
+ <field name="long_name">Preauricular fistulae, congenital</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q11.1-q13.3</field>
+ <field name="info">
+Preauricular fistulae, congenital</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAH">
+ <field name="name">PAH</field>
+ <field name="long_name">phenylalanine hydroxylase</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.1</field>
+ <field name="info">
+Phenylketonuria [MIM:261600]
+Hyperphenylalaninemia, non-PKU mild [MIM:261600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAK3">
+ <field name="name">PAK3</field>
+ <field name="long_name">p21 protein (Cdc42/Rac)-activated kinase 3</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq21.3-q24</field>
+ <field name="info">
+Mental retardation, X-linked 30 [MIM:300558]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PALB2">
+ <field name="name">PALB2</field>
+ <field name="long_name">partner and localizer of BRCA2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12</field>
+ <field name="info">
+Fanconi anemia, complementation group N [MIM:610832]
+Breast cancer, susceptibility to [MIM:114480]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PALLD">
+ <field name="name">PALLD</field>
+ <field name="long_name">palladin, cytoskeletal associated protein</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q32.3</field>
+ <field name="info">
+Pancreatic cancer, susceptibility to, 1 [MIM:606856]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAND1">
+ <field name="name">PAND1</field>
+ <field name="long_name">Panic disorder 1</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q22-q32</field>
+ <field name="info">
+Panic disorder syndrome 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAND2">
+ <field name="name">PAND2</field>
+ <field name="long_name">panic disorder 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q31</field>
+ <field name="info">
+Panic disorder 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAND3">
+ <field name="name">PAND3</field>
+ <field name="long_name">panic disorder 3</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q31-q34</field>
+ <field name="info">
+Panic disorder 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PANK2">
+ <field name="name">PANK2</field>
+ <field name="long_name">pantothenate kinase 2</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p13-p12.3</field>
+ <field name="info">
+Neurodegeneration, pantothenate kinase-associated [MIM:234200]
+HARP syndrome [MIM:607236]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAOD1">
+ <field name="name">PAOD1</field>
+ <field name="long_name">Peripheral arterial occlusive disease 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+Peripheral arterial occlusive disease 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAPA2">
+ <field name="name">PAPA2</field>
+ <field name="long_name">postaxial polydactyly, type A2</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q21-q32</field>
+ <field name="info">
+Postaxial polydactyly, type A2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAPA3">
+ <field name="name">PAPA3</field>
+ <field name="long_name">Polydactyly, postaxial, type A3</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2-p13.1</field>
+ <field name="info">
+Polydactyly, postaxial, type A3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAPA4">
+ <field name="name">PAPA4</field>
+ <field name="long_name">Polydactyly, postaxial, type A4</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22</field>
+ <field name="info">
+Polydactyly, postaxial, type A4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAPSS2">
+ <field name="name">PAPSS2</field>
+ <field name="long_name">3'-phosphoadenosine 5'-phosphosulfate synthase 2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22-q24</field>
+ <field name="info">
+SEMD, Pakistani type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PARK10">
+ <field name="name">PARK10</field>
+ <field name="long_name">Parkinson disease 10</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+Parkinson disease [MIM:168600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PARK12">
+ <field name="name">PARK12</field>
+ <field name="long_name">Parkinson disease (X-linked) 12</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq21-q25</field>
+ <field name="info">
+Parkinson disease 12 [MIM:168600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PARK2">
+ <field name="name">PARK2</field>
+ <field name="long_name">Parkinson disease (autosomal recessive, juvenile) 2, parkin</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25.2-q27</field>
+ <field name="info">
+Parkinson disease, juvenile, type 2 [MIM:600116]
+Adenocarcinoma of lung, somatic [MIM:211980]
+Adenocarcinoma, ovarian, somatic [MIM:604370]
+Leprosy, susceptibility to [MIM:607572]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PARK3">
+ <field name="name">PARK3</field>
+ <field name="long_name">Parkinson disease (autosomal dominant, Lewy body) 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p13</field>
+ <field name="info">
+Parkinson disease, familial [MIM:168600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PARK4">
+ <field name="name">PARK4</field>
+ <field name="long_name">Parkinson disease (autosomal dominant, Lewy body) 4</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21</field>
+ <field name="info">
+Parkinson disease, familial [MIM:168601]
+Parkinson disease 4, autosomal dominant Lewy body [MIM:605543]
+Dementia, Lewy body [MIM:127750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PARK7">
+ <field name="name">PARK7</field>
+ <field name="long_name">Parkinson disease (autosomal recessive, early onset) 7</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Parkinson disease 7, autosomal recessive early-onset [MIM:606324]
+Amyotrophic lateral sclerosis-Parkinsonism/dementia complex 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PARP1">
+ <field name="name">PARP1</field>
+ <field name="long_name">poly (ADP-ribose) polymerase 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42</field>
+ <field name="info">
+Xeroderma pigmentosum</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PASK">
+ <field name="name">PASK</field>
+ <field name="long_name">PAS domain containing serine/threonine kinase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAWR">
+ <field name="name">PAWR</field>
+ <field name="long_name">PRKC, apoptosis, WT1, regulator</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAX1">
+ <field name="name">PAX1</field>
+ <field name="long_name">paired box 1</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAX2">
+ <field name="name">PAX2</field>
+ <field name="long_name">paired box 2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24.3-q25.1</field>
+ <field name="info">
+Optic nerve coloboma with renal disease [MIM:120330]
+Renal hypoplasia, isolated</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAX3">
+ <field name="name">PAX3</field>
+ <field name="long_name">paired box 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35</field>
+ <field name="info">
+Waardenburg syndrome, type I [MIM:193500]
+Waardenburg syndrome, type III [MIM:148820]
+Rhabdomyosarcoma, alveolar [MIM:268220]
+Craniofacial-deafness-hand syndrome [MIM:122880]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAX4">
+ <field name="name">PAX4</field>
+ <field name="long_name">paired box 4</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q32</field>
+ <field name="info">
+Maturity-onset diabetes of the young, type IX [MIM:612225]
+Diabetes mellitus, type 2 [MIM:125853]
+Diabetes mellitus, ketosis-prone [MIM:612227]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAX5">
+ <field name="name">PAX5</field>
+ <field name="long_name">paired box 5</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p13</field>
+ <field name="info">
+Lymphoplasmacytoid lymphoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAX6">
+ <field name="name">PAX6</field>
+ <field name="long_name">paired box 6</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13</field>
+ <field name="info">
+Aniridia [MIM:106210]
+Peters anomaly [MIM:604229]
+Cataract with late-onset corneal dystrophy [MIM:604219]
+Keratitis [MIM:148190]
+Foveal hyperplasia [MIM:136520]
+Ectopia pupillae [MIM:129750]
+Morning glory disc anomaly [MIM:120430]
+Optic nerve hypoplasia [MIM:165550]
+Coloboma, ocular [MIM:120200]
+Coloboma of optic nerve [MIM:120430]
+Gillespie syndrome [MIM:206700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAX7">
+ <field name="name">PAX7</field>
+ <field name="long_name">paired box 7</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2-p36.12</field>
+ <field name="info">
+Rhabdomyosarcoma, alveolar [MIM:268220]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAX8">
+ <field name="name">PAX8</field>
+ <field name="long_name">paired box 8</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q12-q14</field>
+ <field name="info">
+Hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia [MIM:218700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PAX9">
+ <field name="name">PAX9</field>
+ <field name="long_name">paired box 9</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q12-q13</field>
+ <field name="info">
+Tooth agenesis, selective, 3 [MIM:604625]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PBCA">
+ <field name="name">PBCA</field>
+ <field name="long_name">Pancreatic beta cell, agenesis of</field>
+ <field name="chromosome">6</field>
+ <field name="location">6</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, neonatal</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PBX1">
+ <field name="name">PBX1</field>
+ <field name="long_name">pre-B-cell leukemia homeobox 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23</field>
+ <field name="info">
+Leukemia, acute pre-B-cell</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCAP">
+ <field name="name">PCAP</field>
+ <field name="long_name">predisposing for prostate cancer</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42.2-q43</field>
+ <field name="info">
+Prostate cancer, susceptibility to [MIM:176807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCCA">
+ <field name="name">PCCA</field>
+ <field name="long_name">propionyl Coenzyme A carboxylase, alpha polypeptide</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q32</field>
+ <field name="info">
+Propionicacidemia [MIM:606054]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCCB">
+ <field name="name">PCCB</field>
+ <field name="long_name">propionyl Coenzyme A carboxylase, beta polypeptide</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21-q22</field>
+ <field name="info">
+Propionicacidemia [MIM:606054]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCDH15">
+ <field name="name">PCDH15</field>
+ <field name="long_name">protocadherin 15</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21-q22</field>
+ <field name="info">
+Usher syndrome, type 1F [MIM:602083]
+Deafness, autosomal recessive 23 [MIM:609533]
+Usher syndrome, type 1D/F digenic [MIM:601067]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCDH19">
+ <field name="name">PCDH19</field>
+ <field name="long_name">protocadherin 19</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.3</field>
+ <field name="info">
+Epilepsy, female-restricted, with mental retardation [MIM:300088]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCDHA10">
+ <field name="name">PCDHA10</field>
+ <field name="long_name">protocadherin alpha 10</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCK1">
+ <field name="name">PCK1</field>
+ <field name="long_name">phosphoenolpyruvate carboxykinase 1 (soluble)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.31</field>
+ <field name="info">
+Hypoglycemia due to PCK1 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCK2">
+ <field name="name">PCK2</field>
+ <field name="long_name">phosphoenolpyruvate carboxykinase 2 (mitochondrial)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2-q12</field>
+ <field name="info">
+PEPCK deficiency, mitochondrial</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCLD">
+ <field name="name">PCLD</field>
+ <field name="long_name">polycystic liver disease</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2-p13.1</field>
+ <field name="info">
+Polycystic liver disease [MIM:174050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCM1">
+ <field name="name">PCM1</field>
+ <field name="long_name">pericentriolar material 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p22-p21.3</field>
+ <field name="info">
+Thyroid carcinoma, papillary [MIM:188550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCMT1">
+ <field name="name">PCMT1</field>
+ <field name="long_name">protein-L-isoaspartate (D-aspartate) O-methyltransferase</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q22.3-q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCNT">
+ <field name="name">PCNT</field>
+ <field name="long_name">pericentrin</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCSK1">
+ <field name="name">PCSK1</field>
+ <field name="long_name">proprotein convertase subtilisin/kexin type 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q15-q21</field>
+ <field name="info">
+Obesity with impaired prohormone processing [MIM:600955]
+Obesity, susceptiblity to, BMIQ12 [MIM:612362]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCSK2">
+ <field name="name">PCSK2</field>
+ <field name="long_name">proprotein convertase subtilisin/kexin type 2</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PCSK9">
+ <field name="name">PCSK9</field>
+ <field name="long_name">proprotein convertase subtilisin/kexin type 9</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34.1-p32</field>
+ <field name="info">
+Hypercholesterolemia, familial, 3 [MIM:603776]
+Low density lipoprotein cholesterol level QTL 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PC">
+ <field name="name">PC</field>
+ <field name="long_name">pyruvate carboxylase</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.4-q13.5</field>
+ <field name="info">
+Pyruvate carboxylase deficiency [MIM:266150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDB2">
+ <field name="name">PDB2</field>
+ <field name="long_name">Paget disease of bone 2</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21-q22</field>
+ <field name="info">
+Osteosarcoma [MIM:259500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDB4">
+ <field name="name">PDB4</field>
+ <field name="long_name">Paget disease of bone 4</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Paget disease of bone [MIM:602080]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDCD10">
+ <field name="name">PDCD10</field>
+ <field name="long_name">programmed cell death 10</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.1</field>
+ <field name="info">
+Cerebral cavernous malformations 3 [MIM:603285]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDCD1">
+ <field name="name">PDCD1</field>
+ <field name="long_name">programmed cell death 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.3</field>
+ <field name="info">
+Systemic lupus erythematosus, susceptibility to, 2, 605218 [MIM:152700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDE11A">
+ <field name="name">PDE11A</field>
+ <field name="long_name">phosphodiesterase 11A</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31.2</field>
+ <field name="info">
+Pigmented nodular adrenocortical disease, primary, 2 [MIM:610475]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDE4B">
+ <field name="name">PDE4B</field>
+ <field name="long_name">phosphodiesterase 4B, cAMP-specific (phosphodiesterase E4 dunce homolog, Drosophila)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDE4D">
+ <field name="name">PDE4D</field>
+ <field name="long_name">phosphodiesterase 4D, cAMP-specific (phosphodiesterase E3 dunce homolog, Drosophila)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q12</field>
+ <field name="info">
+Stroke, susceptibility to, 1 [MIM:606799]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDE6A">
+ <field name="name">PDE6A</field>
+ <field name="long_name">phosphodiesterase 6A, cGMP-specific, rod, alpha</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.2-q34</field>
+ <field name="info">
+Retinitis pigmentosa, autosomal recessive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDE6B">
+ <field name="name">PDE6B</field>
+ <field name="long_name">phosphodiesterase 6B, cGMP-specific, rod, beta</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.3</field>
+ <field name="info">
+Night blindness, congenital stationary, type 3 [MIM:163500]
+Retinitis pigmentosa 40</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDE6H">
+ <field name="name">PDE6H</field>
+ <field name="long_name">phosphodiesterase 6H, cGMP-specific, cone, gamma</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+Retinal cone dystrophy 3 [MIM:610024]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDE8B">
+ <field name="name">PDE8B</field>
+ <field name="long_name">phosphodiesterase 8B</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13</field>
+ <field name="info">
+Pigmented nodular adrenocortical disease, primary, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDGFB">
+ <field name="name">PDGFB</field>
+ <field name="long_name">platelet-derived growth factor beta polypeptide (simian sarcoma viral (v-sis) oncogene homolog)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.3-q13.1</field>
+ <field name="info">
+Meningioma, SIS-related
+Dermatofibrosarcoma protuberans
+Giant-cell fibroblastoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDGFRA">
+ <field name="name">PDGFRA</field>
+ <field name="long_name">platelet-derived growth factor receptor, alpha polypeptide</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q12</field>
+ <field name="info">
+Gastrointestinal stromal tumor, somatic [MIM:606764]
+Hypereosinophilic syndrome, idiopathic, resistant to imatinib [MIM:607685]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDGFRB">
+ <field name="name">PDGFRB</field>
+ <field name="long_name">platelet-derived growth factor receptor, beta polypeptide</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31-q32</field>
+ <field name="info">
+Myeloproliferative disorder with eosinophilia [MIM:131440]
+Myelomonocytic leukemia, chronic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDGFRL">
+ <field name="name">PDGFRL</field>
+ <field name="long_name">platelet-derived growth factor receptor-like</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p22-p21.3</field>
+ <field name="info">
+Hepatocellular cancer [MIM:114550]
+Colorectal cancer [MIM:114500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDHA1">
+ <field name="name">PDHA1</field>
+ <field name="long_name">pyruvate dehydrogenase (lipoamide) alpha 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.2-p22.1</field>
+ <field name="info">
+Pyruvate dehydrogenase deficiency [MIM:312170]
+Leigh syndrome, X-linked [MIM:308930]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDHB">
+ <field name="name">PDHB</field>
+ <field name="long_name">pyruvate dehydrogenase (lipoamide) beta</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p13-q23</field>
+ <field name="info">
+Pyruvate dehydrogenase E1-beta deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDPK1">
+ <field name="name">PDPK1</field>
+ <field name="long_name">3-phosphoinositide dependent protein kinase-1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDR">
+ <field name="name">PDR</field>
+ <field name="long_name">pigment disorder, reticulate</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22-p21</field>
+ <field name="info">
+Pigment disorder, reticulate</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDSS1">
+ <field name="name">PDSS1</field>
+ <field name="long_name">prenyl (decaprenyl) diphosphate synthase, subunit 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p12.1</field>
+ <field name="info">
+Coenzyme Q10 deficiency [MIM:607426]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDSS2">
+ <field name="name">PDSS2</field>
+ <field name="long_name">prenyl (decaprenyl) diphosphate synthase, subunit 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+Coenzyme Q10 deficiency [MIM:607426]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDX1">
+ <field name="name">PDX1</field>
+ <field name="long_name">pancreatic and duodenal homeobox 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13</field>
+ <field name="info">
+Lacticacidemia due to PDX1 deficiency [MIM:245349]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDXK">
+ <field name="name">PDXK</field>
+ <field name="long_name">pyridoxal (pyridoxine, vitamin B6) kinase</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PDYN">
+ <field name="name">PDYN</field>
+ <field name="long_name">prodynorphin</field>
+ <field name="chromosome">20</field>
+ <field name="location">20pter-p12.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PECAM1">
+ <field name="name">PECAM1</field>
+ <field name="long_name">platelet/endothelial cell adhesion molecule</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEE1">
+ <field name="name">PEE1</field>
+ <field name="long_name">preeclampsia/eclampsia 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p13</field>
+ <field name="info">
+Preeclampsia/eclampsia 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEE2">
+ <field name="name">PEE2</field>
+ <field name="long_name">Preeclampsia/eclampsia 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p25</field>
+ <field name="info">
+Preeclampsia/eclampsia 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEE3">
+ <field name="name">PEE3</field>
+ <field name="long_name">Preeclampsia/eclampsia 3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p13</field>
+ <field name="info">
+Preeclampsia/eclampsia 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PENK">
+ <field name="name">PENK</field>
+ <field name="long_name">proenkephalin</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q23-q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEPD">
+ <field name="name">PEPD</field>
+ <field name="long_name">peptidase D</field>
+ <field name="chromosome">19</field>
+ <field name="location">19cen-q13.11</field>
+ <field name="info">
+Prolidase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PER1">
+ <field name="name">PER1</field>
+ <field name="long_name">period homolog 1 (Drosophila)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PER2">
+ <field name="name">PER2</field>
+ <field name="long_name">period homolog 2 (Drosophila)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.3</field>
+ <field name="info">
+Advanced sleep phase syndrome, familial [MIM:604348]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEX10">
+ <field name="name">PEX10</field>
+ <field name="long_name">peroxisomal biogenesis factor 10</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.32</field>
+ <field name="info">
+Zellweger syndrome [MIM:214100]
+Adrenoleukodystrophy, neonatal [MIM:202370]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEX12">
+ <field name="name">PEX12</field>
+ <field name="long_name">peroxisomal biogenesis factor 12</field>
+ <field name="chromosome">17</field>
+ <field name="location">17</field>
+ <field name="info">
+Peroxisome biogenesis factor 12</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEX13">
+ <field name="name">PEX13</field>
+ <field name="long_name">peroxisomal biogenesis factor 13</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p15</field>
+ <field name="info">
+Zellweger syndrome [MIM:214100]
+Adrenoleukodystrophy, neonatal [MIM:202370]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEX14">
+ <field name="name">PEX14</field>
+ <field name="long_name">peroxisomal biogenesis factor 14</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2</field>
+ <field name="info">
+Zellweger syndrome [MIM:214100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEX16">
+ <field name="name">PEX16</field>
+ <field name="long_name">peroxisomal biogenesis factor 16</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p12-p11.2</field>
+ <field name="info">
+Zellweger syndrome, complementation group 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEX19">
+ <field name="name">PEX19</field>
+ <field name="long_name">peroxisomal biogenesis factor 19</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q22</field>
+ <field name="info">
+Zellweger syndrome [MIM:214100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEX1">
+ <field name="name">PEX1</field>
+ <field name="long_name">peroxisomal biogenesis factor 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21-q22</field>
+ <field name="info">
+Zellweger syndrome-1 [MIM:214100]
+Adrenoleukodystrophy, neonatal [MIM:202370]
+Refsum disease, infantile [MIM:266510]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEX26">
+ <field name="name">PEX26</field>
+ <field name="long_name">peroxisomal biogenesis factor 26</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.21</field>
+ <field name="info">
+Adrenoleukodystrophy, neonatal [MIM:202370]
+Refsum disease, infantile form [MIM:266510]
+Zellweger syndrome [MIM:214100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEX3">
+ <field name="name">PEX3</field>
+ <field name="long_name">peroxisomal biogenesis factor 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23-q24</field>
+ <field name="info">
+Zellweger syndrome, complementation group G [MIM:214100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEX5">
+ <field name="name">PEX5</field>
+ <field name="long_name">peroxisomal biogenesis factor 5</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.3</field>
+ <field name="info">
+Adrenoleukodystrophy, neonatal [MIM:202370]
+Zellweger syndrome [MIM:214100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEX6">
+ <field name="name">PEX6</field>
+ <field name="long_name">peroxisomal biogenesis factor 6</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.1</field>
+ <field name="info">
+Peroxisomal biogenesis disorder, complementation group 4
+Peroxisomal biogenesis disorder, complementation group 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PEX7">
+ <field name="name">PEX7</field>
+ <field name="long_name">peroxisomal biogenesis factor 7</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q22-q24</field>
+ <field name="info">
+Rhizomelic chondrodysplasia punctata, type 1 [MIM:215100]
+Refsum disease [MIM:266500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PFAS">
+ <field name="name">PFAS</field>
+ <field name="long_name">phosphoribosylformylglycinamidine synthase</field>
+ <field name="chromosome">17</field>
+ <field name="location">17</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PFBI">
+ <field name="name">PFBI</field>
+ <field name="long_name">Plasmodium falciparum blood infection levels</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31-q33</field>
+ <field name="info">
+Malaria, intensity of infection</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PFKL">
+ <field name="name">PFKL</field>
+ <field name="long_name">phosphofructokinase, liver</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Hemolytic anemia due to phosphofructokinase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PFKM">
+ <field name="name">PFKM</field>
+ <field name="long_name">phosphofructokinase, muscle</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13.3</field>
+ <field name="info">
+Glycogen storage disease VII [MIM:232800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PGAM1">
+ <field name="name">PGAM1</field>
+ <field name="long_name">phosphoglycerate mutase 1 (brain)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q25.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PGAM2">
+ <field name="name">PGAM2</field>
+ <field name="long_name">phosphoglycerate mutase 2 (muscle)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p13-p12.3</field>
+ <field name="info">
+Myopathy due to phosphoglycerate mutase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PGC">
+ <field name="name">PGC</field>
+ <field name="long_name">progastricsin (pepsinogen C)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3-p21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PGK1P1">
+ <field name="name">PGK1P1</field>
+ <field name="long_name">phosphoglycerate kinase 1, pseudogene 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13</field>
+ <field name="info">
+Phosphoglycerate kinase 1 deficiency [MIM:300653]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PGK1P2">
+ <field name="name">PGK1P2</field>
+ <field name="long_name">phosphoglycerate kinase 1, pseudogene 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13</field>
+ <field name="info">
+Phosphoglycerate kinase 1 deficiency [MIM:300653]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PGK1">
+ <field name="name">PGK1</field>
+ <field name="long_name">phosphoglycerate kinase 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13</field>
+ <field name="info">
+Phosphoglycerate kinase 1 deficiency [MIM:300653]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PGL2">
+ <field name="name">PGL2</field>
+ <field name="long_name">paraganglioma or familial glomus tumors 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.1</field>
+ <field name="info">
+Paragangliomas, familial nonchromaffin, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PGRMC1">
+ <field name="name">PGRMC1</field>
+ <field name="long_name">progesterone receptor membrane component 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22-q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PGR">
+ <field name="name">PGR</field>
+ <field name="long_name">progesterone receptor</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22</field>
+ <field name="info">
+Progesterone resistance [MIM:264080]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHA2A">
+ <field name="name">PHA2A</field>
+ <field name="long_name">Pseudohypoaldosteronism type II (gene A)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31-q42</field>
+ <field name="info">
+Pseudohypoaldosteronism, type II</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHARC">
+ <field name="name">PHARC</field>
+ <field name="long_name">Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p11.21-q12</field>
+ <field name="info">
+Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHB">
+ <field name="name">PHB</field>
+ <field name="long_name">prohibitin</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+Breast cancer, sporadic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHEX">
+ <field name="name">PHEX</field>
+ <field name="long_name">phosphate regulating endopeptidase homolog, X-linked</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.2-p22.1</field>
+ <field name="info">
+Hypophosphatemia, X-linked [MIM:307800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHF11">
+ <field name="name">PHF11</field>
+ <field name="long_name">PHD finger protein 11</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14.1</field>
+ <field name="info">
+IgE levels QTL [MIM:147050]
+Asthma [MIM:600807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHF6">
+ <field name="name">PHF6</field>
+ <field name="long_name">PHD finger protein 6</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26.3</field>
+ <field name="info">
+Borjeson-Forssman-Lehmann syndrome [MIM:301900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHF8">
+ <field name="name">PHF8</field>
+ <field name="long_name">PHD finger protein 8</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.2</field>
+ <field name="info">
+Mental retardation syndrome, X-linked, Siderius type [MIM:300263]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHGDH">
+ <field name="name">PHGDH</field>
+ <field name="long_name">phosphoglycerate dehydrogenase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q12</field>
+ <field name="info">
+Phosphoglycerate dehydrogenase deficiency [MIM:601815]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHKA1">
+ <field name="name">PHKA1</field>
+ <field name="long_name">phosphorylase kinase, alpha 1 (muscle)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13</field>
+ <field name="info">
+Muscle glycogenosis [MIM:300559]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHKA2">
+ <field name="name">PHKA2</field>
+ <field name="long_name">phosphorylase kinase, alpha 2 (liver)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.2-p22.1</field>
+ <field name="info">
+Glycogenosis, X-linked hepatic, type I
+Glycogenosis, X-linked hepatic, type II</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHKB">
+ <field name="name">PHKB</field>
+ <field name="long_name">phosphorylase kinase, beta</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q12-q13</field>
+ <field name="info">
+Phosphorylase kinase deficiency of liver and muscle, autosomal recessive [MIM:261750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHKG2">
+ <field name="name">PHKG2</field>
+ <field name="long_name">phosphorylase kinase, gamma 2 (testis)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12.1-p11.2</field>
+ <field name="info">
+Glycogen storage disease IXc
+Cirrhosis due to liver phosphorylase kinase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHOBS">
+ <field name="name">PHOBS</field>
+ <field name="long_name">Phobia, specific</field>
+ <field name="chromosome">14</field>
+ <field name="location">14</field>
+ <field name="info">
+Phobia, specific</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHOX2A">
+ <field name="name">PHOX2A</field>
+ <field name="long_name">paired-like homeobox 2a</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.3-q13.4</field>
+ <field name="info">
+Fibrosis of extraocular muscles, congenital, 2 [MIM:602078]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHOX2B">
+ <field name="name">PHOX2B</field>
+ <field name="long_name">paired-like homeobox 2b</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p12</field>
+ <field name="info">
+Central hypoventilation syndrome, congenital [MIM:209880]
+Hirschsprung disease, short-segment [MIM:142623]
+Neuroblastoma [MIM:256700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PHYH">
+ <field name="name">PHYH</field>
+ <field name="long_name">phytanoyl-CoA 2-hydroxylase</field>
+ <field name="chromosome">10</field>
+ <field name="location">10pter-p11.2</field>
+ <field name="info">
+Refsum disease [MIM:266500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PICK1">
+ <field name="name">PICK1</field>
+ <field name="long_name">protein interacting with PRKCA 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.3-q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PIGA">
+ <field name="name">PIGA</field>
+ <field name="long_name">phosphatidylinositol glycan anchor biosynthesis, class A</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.1</field>
+ <field name="info">
+Paroxysmal nocturnal hemoglobinuria</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PIGM">
+ <field name="name">PIGM</field>
+ <field name="long_name">phosphatidylinositol glycan anchor biosynthesis, class M</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23.2</field>
+ <field name="info">
+Glycosylphosphatidylinositol deficiency [MIM:610293]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PIGR">
+ <field name="name">PIGR</field>
+ <field name="long_name">polymeric immunoglobulin receptor</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31-q42</field>
+ <field name="info">
+IgA nephropathy, susceptibility to [MIM:161950]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PIK3C2G">
+ <field name="name">PIK3C2G</field>
+ <field name="long_name">phosphoinositide-3-kinase, class 2, gamma polypeptide</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PIK3CA">
+ <field name="name">PIK3CA</field>
+ <field name="long_name">phosphoinositide-3-kinase, catalytic, alpha polypeptide</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.3</field>
+ <field name="info">
+Ovarian cancer, somatic [MIM:604370]
+Breast cancer, somatic [MIM:114480]
+Colorectal cancer, somatic [MIM:114500]
+Gastric cancer, somatic [MIM:137215]
+Hepatocellular carcinoma, somatic [MIM:114550]
+Nonsmall cell lung cancer, somatic [MIM:211980]
+Keratosis, seborrheic, somatic [MIM:182000]
+Nevus, epidermal [MIM:162900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PIK3CB">
+ <field name="name">PIK3CB</field>
+ <field name="long_name">phosphoinositide-3-kinase, catalytic, beta polypeptide</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PIK3CD">
+ <field name="name">PIK3CD</field>
+ <field name="long_name">phosphoinositide-3-kinase, catalytic, delta polypeptide</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PIK3R1">
+ <field name="name">PIK3R1</field>
+ <field name="long_name">phosphoinositide-3-kinase, regulatory subunit 1 (alpha)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PIN1">
+ <field name="name">PIN1</field>
+ <field name="long_name">peptidylprolyl cis/trans isomerase, NIMA-interacting 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PINK1">
+ <field name="name">PINK1</field>
+ <field name="long_name">PTEN induced putative kinase 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Parkinson disease 6, early onset [MIM:605909]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PIP5K1C">
+ <field name="name">PIP5K1C</field>
+ <field name="long_name">phosphatidylinositol-4-phosphate 5-kinase, type I, gamma</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Lethal congenital contractural syndrome 3 [MIM:611369]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PITPNM3">
+ <field name="name">PITPNM3</field>
+ <field name="long_name">PITPNM family member 3</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13</field>
+ <field name="info">
+Cone-rod dystrophy 5 [MIM:600977]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PITX1">
+ <field name="name">PITX1</field>
+ <field name="long_name">paired-like homeodomain 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Clubfoot, congenital [MIM:119800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PITX2">
+ <field name="name">PITX2</field>
+ <field name="long_name">paired-like homeodomain 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q25-q26</field>
+ <field name="info">
+Axenfeld-Rieger syndrome, type 1 [MIM:180500]
+Iridogoniodysgenesis, type 2 [MIM:137600]
+Ring dermoid of cornea [MIM:180550]
+Peters anomaly [MIM:604229]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PITX3">
+ <field name="name">PITX3</field>
+ <field name="long_name">paired-like homeodomain 3</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q25</field>
+ <field name="info">
+Anterior segment mesenchymal dysgenesis [MIM:107250]
+Cataract, posterior polar, 4 [MIM:610623]
+Cataract, congenital
+Cataract, posterior polar, 4, syndromic [MIM:610623]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PKC">
+ <field name="name">PKC</field>
+ <field name="long_name">Paroxysmal kinesigenic choreoathetosis</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p11.2-q12.1</field>
+ <field name="info">
+Paroxysmal kinesigenic choreoathetosis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PKD1L1">
+ <field name="name">PKD1L1</field>
+ <field name="long_name">polycystic kidney disease 1 like 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p13-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PKD1">
+ <field name="name">PKD1</field>
+ <field name="long_name">polycystic kidney disease 1 (autosomal dominant)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3-p13.12</field>
+ <field name="info">
+Polycystic kidney disease, adult type I [MIM:173900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PKD2">
+ <field name="name">PKD2</field>
+ <field name="long_name">polycystic kidney disease 2 (autosomal dominant)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21-q23</field>
+ <field name="info">
+Polycystic kidney disease, adult, type II</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PKDTS">
+ <field name="name">PKDTS</field>
+ <field name="long_name">polycystic kidney disease, infantile severe, with tuberous sclerosis</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+Polycystic kidney disease, infantile severe, with tuberous sclerosis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PKHD1">
+ <field name="name">PKHD1</field>
+ <field name="long_name">polycystic kidney and hepatic disease 1 (autosomal recessive)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.1-p12</field>
+ <field name="info">
+Polycystic kidney and hepatic disease [MIM:263200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PKLR">
+ <field name="name">PKLR</field>
+ <field name="long_name">pyruvate kinase, liver and RBC</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Pyruvate kinase deficiency [MIM:266200]
+Adenosine triphosphate, elevated, of erythrocytes [MIM:102900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PKN3">
+ <field name="name">PKN3</field>
+ <field name="long_name">protein kinase N3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PKP1">
+ <field name="name">PKP1</field>
+ <field name="long_name">plakophilin 1 (ectodermal dysplasia/skin fragility syndrome)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+Ectodermal dysplasia/skin fragility syndrome [MIM:604536]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PKP2">
+ <field name="name">PKP2</field>
+ <field name="long_name">plakophilin 2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p11</field>
+ <field name="info">
+Arrhythmogenic right ventricular dysplasia, familial, 9 [MIM:609040]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLA2G2A">
+ <field name="name">PLA2G2A</field>
+ <field name="long_name">phospholipase A2, group IIA (platelets, synovial fluid)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p35</field>
+ <field name="info">
+Colorectal cancer, sporadic [MIM:114500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLA2G4A">
+ <field name="name">PLA2G4A</field>
+ <field name="long_name">phospholipase A2, group IVA (cytosolic, calcium-dependent)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q25</field>
+ <field name="info">
+Phospholipase A2, group IV A, deficiency of</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLA2G6">
+ <field name="name">PLA2G6</field>
+ <field name="long_name">phospholipase A2, group VI (cytosolic, calcium-independent)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.1</field>
+ <field name="info">
+Infantile neuroaxonal dystrophy 1 [MIM:256600]
+Neurodegeneration with brain iron accumulation [MIM:610217]
+Karak syndrome [MIM:608395]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLA2G7">
+ <field name="name">PLA2G7</field>
+ <field name="long_name">phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.2-p12</field>
+ <field name="info">
+Platelet-activating factor acetylhydrolase deficiency
+Asthma, susceptibility to [MIM:600807]
+Atopy, susceptibility to [MIM:147050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLAG1">
+ <field name="name">PLAG1</field>
+ <field name="long_name">pleiomorphic adenoma gene 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q12</field>
+ <field name="info">
+Adenomas, salivary gland pleomorphic [MIM:181030]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLAGL1">
+ <field name="name">PLAGL1</field>
+ <field name="long_name">pleiomorphic adenoma gene-like 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q24</field>
+ <field name="info">
+Diabetes mellitus, transient neonatal [MIM:601410]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLAT">
+ <field name="name">PLAT</field>
+ <field name="long_name">plasminogen activator, tissue</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p12</field>
+ <field name="info">
+Thrombophilia, familial, due to decreased release of PLAT [MIM:612348]
+Hyperfibrinolysis, familial, due to increased release of PLAT [MIM:612348]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLAU">
+ <field name="name">PLAU</field>
+ <field name="long_name">plasminogen activator, urokinase</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+Alzheimer disease, late-onset, susceptibility to [MIM:104300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLCB2">
+ <field name="name">PLCB2</field>
+ <field name="long_name">phospholipase C, beta 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15</field>
+ <field name="info">
+Platelet PLC beta-2 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLCD1">
+ <field name="name">PLCD1</field>
+ <field name="long_name">phospholipase C, delta 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p22-p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLCE1">
+ <field name="name">PLCE1</field>
+ <field name="long_name">phospholipase C, epsilon 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23</field>
+ <field name="info">
+Nephrotic syndrome, type 3 [MIM:610725]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLD2">
+ <field name="name">PLD2</field>
+ <field name="long_name">phospholipase D2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLEC1">
+ <field name="name">PLEC1</field>
+ <field name="long_name">plectin 1, intermediate filament binding protein 500kDa</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24</field>
+ <field name="info">
+Muscular dystrophy with epidermolysis bullosa simplex [MIM:226670]
+Epidermolysis bullosa simplex, Ogna type [MIM:131950]
+Epidermolysis bullosa simplex with pyloric atresia [MIM:612138]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLEKHA1">
+ <field name="name">PLEKHA1</field>
+ <field name="long_name">pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q25.3-q26.2</field>
+ <field name="info">
+Age-related maculopathy, susceptibility to [MIM:603075]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLEKHG4">
+ <field name="name">PLEKHG4</field>
+ <field name="long_name">pleckstrin homology domain containing, family G (with RhoGef domain) member 4</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22.1</field>
+ <field name="info">
+Spinocerebellar ataxia 4, pure Japanese type [MIM:117210]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLEKHG5">
+ <field name="name">PLEKHG5</field>
+ <field name="long_name">pleckstrin homology domain containing, family G (with RhoGef domain) member 5</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Spinal muscular atrophy, distal, autosomal recessive, 4 [MIM:611067]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLEKHM1">
+ <field name="name">PLEKHM1</field>
+ <field name="long_name">pleckstrin homology domain containing, family M (with RUN domain) member 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.3</field>
+ <field name="info">
+Osteopetrosis, autosomal recessive 6 [MIM:611497]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLF">
+ <field name="name">PLF</field>
+ <field name="long_name">Pulmonary function</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21-q22</field>
+ <field name="info">
+Pulmonary function</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLG">
+ <field name="name">PLG</field>
+ <field name="long_name">plasminogen</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q26</field>
+ <field name="info">
+Plasminogen Tochigi disease
+Thrombophilia, dysplasminogenemic
+Plasminogen deficiency, types I and II
+Conjunctivitis, ligneous [MIM:217090]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLIN">
+ <field name="name">PLIN</field>
+ <field name="long_name">perilipin</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLN">
+ <field name="name">PLN</field>
+ <field name="long_name">phospholamban</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q22.1</field>
+ <field name="info">
+Cardiomyopathy, dilated, 1P [MIM:609909]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLOD1">
+ <field name="name">PLOD1</field>
+ <field name="long_name">procollagen-lysine 1, 2-oxoglutarate 5-dioxygenase 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3-p36.2</field>
+ <field name="info">
+Ehlers-Danlos syndrome, type VI [MIM:225400]
+Nevo syndrome [MIM:601451]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLOD2">
+ <field name="name">PLOD2</field>
+ <field name="long_name">procollagen-lysine, 2-oxoglutarate 5-dioxygenase 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q23-q24</field>
+ <field name="info">
+Bruck syndrome 2 [MIM:609220]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLOD3">
+ <field name="name">PLOD3</field>
+ <field name="long_name">procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22</field>
+ <field name="info">
+Lysyl hydroxylase 3 deficiency [MIM:612394]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLP1">
+ <field name="name">PLP1</field>
+ <field name="long_name">proteolipid protein 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22</field>
+ <field name="info">
+Pelizaeus-Merzbacher disease [MIM:312080]
+Spastic paraplegia-2 [MIM:312920]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLP2">
+ <field name="name">PLP2</field>
+ <field name="long_name">proteolipid protein 2 (colonic epithelium-enriched)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23-p11.22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLSA1">
+ <field name="name">PLSA1</field>
+ <field name="long_name">Primary lateral sclerosis, adult, 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16</field>
+ <field name="info">
+Primary lateral sclerosis, adult, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLTP">
+ <field name="name">PLTP</field>
+ <field name="long_name">phospholipid transfer protein</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q12-q13.1</field>
+ <field name="info">
+High density lipoprotein cholesterol level QTL 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PLUNC">
+ <field name="name">PLUNC</field>
+ <field name="long_name">palate, lung and nasal epithelium associated</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PML">
+ <field name="name">PML</field>
+ <field name="long_name">promyelocytic leukemia</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22</field>
+ <field name="info">
+Leukemia, acute promyelocytic, PML/RARA type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PMM2">
+ <field name="name">PMM2</field>
+ <field name="long_name">phosphomannomutase 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3-p13.2</field>
+ <field name="info">
+Carbohydrate-deficient glycoprotein syndrome, type I [MIM:212065]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PMP22">
+ <field name="name">PMP22</field>
+ <field name="long_name">peripheral myelin protein 22</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 1A [MIM:118220]
+Dejerine-Sottas disease [MIM:145900]
+Neuropathy, recurrent, with pressure palsies [MIM:162500]
+Charcot-Marie-Tooth disease, type 1E [MIM:118300]
+Roussy-Levy syndrome [MIM:180800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PMS1">
+ <field name="name">PMS1</field>
+ <field name="long_name">PMS1 postmeiotic segregation increased 1 (S. cerevisiae)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31-q33</field>
+ <field name="info">
+Colorectal cancer, hereditary nonpolyposis, type 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PMS2">
+ <field name="name">PMS2</field>
+ <field name="long_name">PMS2 postmeiotic segregation increased 2 (S. cerevisiae)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p22</field>
+ <field name="info">
+Mismatch repair cancer syndrome [MIM:276300]
+Colorectal cancer, hereditary nonpolyposis, type 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PNKD2">
+ <field name="name">PNKD2</field>
+ <field name="long_name">paroxysmal nonkinesigenic dyskinesia 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31</field>
+ <field name="info">
+Paroxysmal nonkinesigenic dyskinesia 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PNKD">
+ <field name="name">PNKD</field>
+ <field name="long_name">paroxysmal nonkinesigenic dyskinesia</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35</field>
+ <field name="info">
+Paroxysmal nonkinesigenic dyskinesia [MIM:118800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PNLIP">
+ <field name="name">PNLIP</field>
+ <field name="long_name">pancreatic lipase</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q26.1</field>
+ <field name="info">
+Pancreatic lipase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PNMT">
+ <field name="name">PNMT</field>
+ <field name="long_name">phenylethanolamine N-methyltransferase</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+Hypertension, essential [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PNPLA2">
+ <field name="name">PNPLA2</field>
+ <field name="long_name">patatin-like phospholipase domain containing 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Neutral lipid storage disease with myopathy [MIM:610717]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PNPLA6">
+ <field name="name">PNPLA6</field>
+ <field name="long_name">patatin-like phospholipase domain containing 6</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Spastic paraplegia 39 [MIM:612020]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PNPO">
+ <field name="name">PNPO</field>
+ <field name="long_name">pyridoxamine 5'-phosphate oxidase</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.32</field>
+ <field name="info">
+Pyridoxamine 5'-phosphate oxidase deficiency [MIM:610090]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="POLB">
+ <field name="name">POLB</field>
+ <field name="long_name">polymerase (DNA directed), beta</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="POLD1">
+ <field name="name">POLD1</field>
+ <field name="long_name">polymerase (DNA directed), delta 1, catalytic subunit 125kDa</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3-q13.4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="POLE2">
+ <field name="name">POLE2</field>
+ <field name="long_name">polymerase (DNA directed), epsilon 2 (p59 subunit)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q13-q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="POLG2">
+ <field name="name">POLG2</field>
+ <field name="long_name">polymerase (DNA directed), gamma 2, accessory subunit</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23-q24</field>
+ <field name="info">
+Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4 [MIM:610131]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="POLG">
+ <field name="name">POLG</field>
+ <field name="long_name">polymerase (DNA directed), gamma</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q25</field>
+ <field name="info">
+Progressive external ophthalmoplegia, autosomal recessive [MIM:258450]
+Progressive external ophthalmoplegia, autosomal dominant, with or without hypogonadiam [MIM:157640]
+Alpers syndrome [MIM:203700]
+Spinocerebellar ataxia with epilepsy [MIM:607459]
+Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis [MIM:607459]
+MNGIE without leukoencephalopathy [MIM:603041]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="POLH">
+ <field name="name">POLH</field>
+ <field name="long_name">polymerase (DNA directed), eta</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.1-p12</field>
+ <field name="info">
+Xeroderma pigmentosum, variant type [MIM:278750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="POMC">
+ <field name="name">POMC</field>
+ <field name="long_name">proopiomelanocortin</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p23.3</field>
+ <field name="info">
+Obesity, adrenal insufficiency, and red hair due to POMC deficiency [MIM:609734]
+Obesity, early-onset, susceptibility to [MIM:601665]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="POMGNT1">
+ <field name="name">POMGNT1</field>
+ <field name="long_name">protein O-linked mannose beta1,2-N-acetylglucosaminyltransferase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34-p33</field>
+ <field name="info">
+Muscle-eye-brain disease [MIM:253280]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="POMT1">
+ <field name="name">POMT1</field>
+ <field name="long_name">protein-O-mannosyltransferase 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.1</field>
+ <field name="info">
+Walker-Warburg syndrome [MIM:236670]
+Muscular dystrophy, limb-girdle, type 2K [MIM:609308]
+Muscular dystrophy, congenital, plus mental retardation [MIM:236670]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="POMT2">
+ <field name="name">POMT2</field>
+ <field name="long_name">protein-O-mannosyltransferase 2</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3</field>
+ <field name="info">
+Walker-Warburg syndrome [MIM:236670]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PON1">
+ <field name="name">PON1</field>
+ <field name="long_name">paraoxonase 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.3</field>
+ <field name="info">
+Coronary artery disease, susceptibility to
+Coronary artery spasm, susceptibility to
+Organophosphate poisoning, sensitivity to (3) 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PON2">
+ <field name="name">PON2</field>
+ <field name="long_name">paraoxonase 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.3</field>
+ <field name="info">
+Coronary artery disease, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PON3">
+ <field name="name">PON3</field>
+ <field name="long_name">paraoxonase 3</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PORCN">
+ <field name="name">PORCN</field>
+ <field name="long_name">porcupine homolog (Drosophila)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23</field>
+ <field name="info">
+Focal dermal hypoplasia [MIM:305600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PORC">
+ <field name="name">PORC</field>
+ <field name="long_name">porphyria, acute; Chester type</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.1</field>
+ <field name="info">
+Porphyria, Chester type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="POR">
+ <field name="name">POR</field>
+ <field name="long_name">P450 (cytochrome) oxidoreductase</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.2</field>
+ <field name="info">
+Antley-Bixler syndrome-like with disordered steroidogenesis [MIM:201750]
+Adrenal hyperplasia, congenital, due to combined P450C17 and P450C21 deficiency [MIM:201750]
+POR deficiency [MIM:201750]
+Disordered steroidogenesis, isolated [MIM:201750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="POU1F1">
+ <field name="name">POU1F1</field>
+ <field name="long_name">POU class 1 homeobox 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p11</field>
+ <field name="info">
+Pituitary hormone deficiency, combined</field>
+</record>
+<record model="gnuhealth.disease.gene" id="POU3F4">
+ <field name="name">POU3F4</field>
+ <field name="long_name">POU class 3 homeobox 4</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq21.1</field>
+ <field name="info">
+Deafness, X-linked 2 [MIM:304400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="POU4F3">
+ <field name="name">POU4F3</field>
+ <field name="long_name">POU class 4 homeobox 3</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Deafness, autosomal dominant 15 [MIM:602459]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="POU6F2">
+ <field name="name">POU6F2</field>
+ <field name="long_name">POU class 6 homeobox 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14-p13</field>
+ <field name="info">
+Wilms tumor susceptibility-5 [MIM:601583]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPARA">
+ <field name="name">PPARA</field>
+ <field name="long_name">peroxisome proliferator-activated receptor alpha</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12-q13.1</field>
+ <field name="info">
+Hyperapobetalipoproteinemia, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPARD">
+ <field name="name">PPARD</field>
+ <field name="long_name">peroxisome proliferator-activated receptor delta</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.2-p21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPARGC1A">
+ <field name="name">PPARGC1A</field>
+ <field name="long_name">peroxisome proliferator-activated receptor gamma, coactivator 1 alpha</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPARGC1B">
+ <field name="name">PPARGC1B</field>
+ <field name="long_name">peroxisome proliferator-activated receptor gamma, coactivator 1 beta</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q33</field>
+ <field name="info">
+Obesity, variation in [MIM:601665]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPARG">
+ <field name="name">PPARG</field>
+ <field name="long_name">peroxisome proliferator-activated receptor gamma</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25</field>
+ <field name="info">
+Obesity, severe [MIM:601665]
+Obesity, resistance to
+Glioblastoma, susceptibility to [MIM:137800]
+Insulin resistance, severe, digenic [MIM:604367]
+Lipodystrophy, familial partial, type 3 [MIM:604367]
+Carotid intimal medial thickness 1 [MIM:609338]
+Diabetes, type 2 [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPAT">
+ <field name="name">PPAT</field>
+ <field name="long_name">phosphoribosyl pyrophosphate amidotransferase</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPIA">
+ <field name="name">PPIA</field>
+ <field name="long_name">peptidylprolyl isomerase A (cyclophilin A)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPIG">
+ <field name="name">PPIG</field>
+ <field name="long_name">peptidylprolyl isomerase G (cyclophilin G)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPKB">
+ <field name="name">PPKB</field>
+ <field name="long_name">palmoplantar keratoderma, Bothnia type</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q11-q13</field>
+ <field name="info">
+Palmoplantar keratoderma, Bothnia type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPM1D">
+ <field name="name">PPM1D</field>
+ <field name="long_name">protein phosphatase 1D magnesium-dependent, delta isoform</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q22-q23</field>
+ <field name="info">
+Breast cancer [MIM:114480]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPM2C">
+ <field name="name">PPM2C</field>
+ <field name="long_name">protein phosphatase 2C, magnesium-dependent, catalytic subunit</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q22.1</field>
+ <field name="info">
+Pyruvate dehydrogenase phosphatase deficiency [MIM:608782]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPOX">
+ <field name="name">PPOX</field>
+ <field name="long_name">protoporphyrinogen oxidase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q22</field>
+ <field name="info">
+Porphyria variegata [MIM:176200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPP1R3A">
+ <field name="name">PPP1R3A</field>
+ <field name="long_name">protein phosphatase 1, regulatory (inhibitor) subunit 3A</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.23-q21.11</field>
+ <field name="info">
+Insulin resistance, severe, digenic [MIM:604367]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPP2R1B">
+ <field name="name">PPP2R1B</field>
+ <field name="long_name">protein phosphatase 2 (formerly 2A), regulatory subunit A, beta isoform</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22-q24</field>
+ <field name="info">
+Lung cancer [MIM:211980]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPP2R2B">
+ <field name="name">PPP2R2B</field>
+ <field name="long_name">protein phosphatase 2 (formerly 2A), regulatory subunit B, beta isoform</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31-q33</field>
+ <field name="info">
+Spinocerebellar ataxia 12 [MIM:604326]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPPD1">
+ <field name="name">PPPD1</field>
+ <field name="long_name">Porokeratosis, palmar, plantar, and disseminated 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.1-q24.2</field>
+ <field name="info">
+Porokeratosis, palmar, plantar, and disseminated 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPR2">
+ <field name="name">PPR2</field>
+ <field name="long_name">Photoparoxysmal response 2</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q31.3</field>
+ <field name="info">
+Photoparoxysmal response 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPR3">
+ <field name="name">PPR3</field>
+ <field name="long_name">photoparoxysmal response 3</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q32</field>
+ <field name="info">
+Photoparoxysmal response 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPR">
+ <field name="name">PPR</field>
+ <field name="long_name">photoparoxysmal response</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p21-p16</field>
+ <field name="info">
+Leigh syndrome, French-Canadian type [MIM:220111]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PPT1">
+ <field name="name">PPT1</field>
+ <field name="long_name">palmitoyl-protein thioesterase 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+Ceroid lipofuscinosis, neuronal-1, infantile [MIM:256730]
+Ceroid lipofuscinosis, neuronal, variant juvenile type, with granular osmiophilic deposits</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PQBP1">
+ <field name="name">PQBP1</field>
+ <field name="long_name">polyglutamine binding protein 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23</field>
+ <field name="info">
+Renpenning syndrome [MIM:309500]
+Golabi-Ito-Hall syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRB1">
+ <field name="name">PRB1</field>
+ <field name="long_name">proline-rich protein BstNI subfamily 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRB3">
+ <field name="name">PRB3</field>
+ <field name="long_name">proline-rich protein BstNI subfamily 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRB4">
+ <field name="name">PRB4</field>
+ <field name="long_name">proline-rich protein BstNI subfamily 4</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRBNS">
+ <field name="name">PRBNS</field>
+ <field name="long_name">Pierre Robin syndrome</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q24.3-q25.1</field>
+ <field name="info">
+Pierre Robin syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRCC">
+ <field name="name">PRCC</field>
+ <field name="long_name">papillary renal cell carcinoma (translocation-associated)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Renal cell carcinoma, papillary, 1 [MIM:605074]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRCD">
+ <field name="name">PRCD</field>
+ <field name="long_name">progressive rod-cone degeneration</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q22</field>
+ <field name="info">
+Retinitis pigmentosa 36 [MIM:610599]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRDM2">
+ <field name="name">PRDM2</field>
+ <field name="long_name">PR domain containing 2, with ZNF domain</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRF1">
+ <field name="name">PRF1</field>
+ <field name="long_name">perforin 1 (pore forming protein)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22</field>
+ <field name="info">
+Hemophagocytic lymphohistiocytosis, familial, 2 [MIM:603553]
+Lymphoma, non-Hodgkin [MIM:605027]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRG4">
+ <field name="name">PRG4</field>
+ <field name="long_name">proteoglycan 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q24-q25</field>
+ <field name="info">
+Camptodactyly-arthropathy-coxa vara-pericarditis syndrome [MIM:208250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRICKLE1">
+ <field name="name">PRICKLE1</field>
+ <field name="long_name">prickle homolog 1 (Drosophila)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q12</field>
+ <field name="info">
+Epilepsy, progressive myoclonic 1B [MIM:612437]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRKAA2">
+ <field name="name">PRKAA2</field>
+ <field name="long_name">protein kinase, AMP-activated, alpha 2 catalytic subunit</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRKAG2">
+ <field name="name">PRKAG2</field>
+ <field name="long_name">protein kinase, AMP-activated, gamma 2 non-catalytic subunit</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q36</field>
+ <field name="info">
+Wolff-Parkinson-White syndrome [MIM:194200]
+Cardiomyopathy, hypertrophic 6, with WPW [MIM:600858]
+Glycogen storage disease of heart, lethal congenital [MIM:261740]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRKAR1A">
+ <field name="name">PRKAR1A</field>
+ <field name="long_name">protein kinase, cAMP-dependent, regulatory, type I, alpha (tissue specific extinguisher 1)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23-q24</field>
+ <field name="info">
+Carney complex, type 1 [MIM:160980]
+Myxoma, intracardiac [MIM:255960]
+Thyroid carcinoma, papillary [MIM:188550]
+Pigmented adrenocortical disease, primary, 1 [MIM:610489]
+Adrenocortical tumor, somatic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRKCA">
+ <field name="name">PRKCA</field>
+ <field name="long_name">protein kinase C, alpha</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q22-q23.2</field>
+ <field name="info">
+Pituitary tumor, invasive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRKCG">
+ <field name="name">PRKCG</field>
+ <field name="long_name">protein kinase C, gamma</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+Spinocerebellar ataxia 14 [MIM:605361]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRKCH">
+ <field name="name">PRKCH</field>
+ <field name="long_name">protein kinase C, eta</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q22-q23</field>
+ <field name="info">
+Cerebral infarction, susceptibility to [MIM:601367]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRKCSH">
+ <field name="name">PRKCSH</field>
+ <field name="long_name">protein kinase C substrate 80K-H</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2-p13.1</field>
+ <field name="info">
+Polycystic liver disease [MIM:174050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRKDC">
+ <field name="name">PRKDC</field>
+ <field name="long_name">protein kinase, DNA-activated, catalytic polypeptide</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRKRA">
+ <field name="name">PRKRA</field>
+ <field name="long_name">protein kinase, interferon-inducible double stranded RNA dependent activator</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31.3</field>
+ <field name="info">
+Dystonia 16 [MIM:612067]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRLR">
+ <field name="name">PRLR</field>
+ <field name="long_name">prolactin receptor</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRM1">
+ <field name="name">PRM1</field>
+ <field name="long_name">protamine 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRM2">
+ <field name="name">PRM2</field>
+ <field name="long_name">protamine 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRND">
+ <field name="name">PRND</field>
+ <field name="long_name">prion protein 2 (dublet)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20pter-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRNP">
+ <field name="name">PRNP</field>
+ <field name="long_name">prion protein</field>
+ <field name="chromosome">20</field>
+ <field name="location">20pter-p12</field>
+ <field name="info">
+Creutzfeldt-Jakob disease [MIM:123400]
+Gerstmann-Straussler disease [MIM:137440]
+Insomnia, fatal familial [MIM:600072]
+Prion disease with protracted course [MIM:606688]
+Huntington disease-like 1 [MIM:603218]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PROCR">
+ <field name="name">PROCR</field>
+ <field name="long_name">protein C receptor, endothelial (EPCR)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PROC">
+ <field name="name">PROC</field>
+ <field name="long_name">protein C (inactivator of coagulation factors Va and VIIIa)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q13-q14</field>
+ <field name="info">
+Thrombophilia due to protein C deficiency, autosomal dominant [MIM:176860]
+Thrombophilia due to protein C deficiency, autosomal recessive [MIM:612304]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRODH2">
+ <field name="name">PRODH2</field>
+ <field name="long_name">proline dehydrogenase (oxidase) 2</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+Hyperprolinemia, type I [MIM:239500]
+Schizophrenia, susceptibility to, 4 [MIM:600850]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRODH">
+ <field name="name">PRODH</field>
+ <field name="long_name">proline dehydrogenase (oxidase) 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+Hyperprolinemia, type I [MIM:239500]
+Schizophrenia, susceptibility to, 4 [MIM:600850]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PROK2">
+ <field name="name">PROK2</field>
+ <field name="long_name">prokineticin 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.1</field>
+ <field name="info">
+Kallmann syndrome 4 [MIM:610628]
+Hypogonadism, hypogonadotropic [MIM:146110]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PROKR2">
+ <field name="name">PROKR2</field>
+ <field name="long_name">prokineticin receptor 2</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p13</field>
+ <field name="info">
+Kallmann syndrome 3 [MIM:244200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PROM1">
+ <field name="name">PROM1</field>
+ <field name="long_name">prominin 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15.3</field>
+ <field name="info">
+Retinitis pigmentosa-41 [MIM:612095]
+Cone-rod dystrophy 12 [MIM:612657]
+Stargardt disease 4 [MIM:603786]
+Macular dystrophy, retinal, 2 [MIM:608051]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PROP1">
+ <field name="name">PROP1</field>
+ <field name="long_name">PROP paired-like homeobox 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q</field>
+ <field name="info">
+Pituitary hormone deficiency, combined</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PROS1">
+ <field name="name">PROS1</field>
+ <field name="long_name">protein S (alpha)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q11.2</field>
+ <field name="info">
+Thrombophilia due to protein S deficiency [MIM:612336]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PROSP">
+ <field name="name">PROSP</field>
+ <field name="long_name">protein S pseudogene (beta)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q11.2</field>
+ <field name="info">
+Thrombophilia due to protein S deficiency [MIM:612336]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRPF31">
+ <field name="name">PRPF31</field>
+ <field name="long_name">PRP31 pre-mRNA processing factor 31 homolog (S. cerevisiae)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+Retinitis pigmentosa-11 [MIM:600138]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRPF8">
+ <field name="name">PRPF8</field>
+ <field name="long_name">PRP8 pre-mRNA processing factor 8 homolog (S. cerevisiae)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.3</field>
+ <field name="info">
+Retinitis pigmentosa-13 [MIM:600059]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRPH2">
+ <field name="name">PRPH2</field>
+ <field name="long_name">peripherin 2 (retinal degeneration, slow)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.1-cen</field>
+ <field name="info">
+Retinitis pigmentosa-7 [MIM:608133]
+Retinitis punctata albescens [MIM:136880]
+Butterfly dystrophy, retinal [MIM:169150]
+Macular dystrophy, vitelliform [MIM:608161]
+Foveomacular dystrophy, adult-onset, with choroidal neovascularization [MIM:608161]
+Macular dystrophy
+Retinitis pigmentosa, digenic [MIM:608133]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRPH">
+ <field name="name">PRPH</field>
+ <field name="long_name">peripherin</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q12-q13</field>
+ <field name="info">
+Amyotrophic lateral sclerosis, susceptibility to [MIM:105400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRPS1">
+ <field name="name">PRPS1</field>
+ <field name="long_name">phosphoribosyl pyrophosphate synthetase 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22-q24</field>
+ <field name="info">
+Gout, PRPS-related [MIM:300661]
+Phosphoribosylpyrophosphate synthetase superactivity [MIM:300661]
+Charcot-Marie-Tooth disease, X-linked recessive, 5 [MIM:311070]
+Arts syndrome [MIM:301835]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRR1">
+ <field name="name">PRR1</field>
+ <field name="long_name">proline rich 1 (prostatic)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23-q24</field>
+ <field name="info">
+Ectodermal dysplasia, Margarita Island type [MIM:225060]
+Zlotogora-Ogur syndrome [MIM:225000]
+Cleft lip/palate ectodermal dysplasia syndrome [MIM:225000]
+Orofacial cleft 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRSS12">
+ <field name="name">PRSS12</field>
+ <field name="long_name">protease, serine, 12 (neurotrypsin, motopsin)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q25-q26</field>
+ <field name="info">
+Mental retardation, autosomal recessive 1 [MIM:249500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRSS1">
+ <field name="name">PRSS1</field>
+ <field name="long_name">protease, serine, 1 (trypsin 1)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q35</field>
+ <field name="info">
+Trypsinogen deficiency
+Pancreatitis, hereditary [MIM:167800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRSS2">
+ <field name="name">PRSS2</field>
+ <field name="long_name">protease, serine, 2 (trypsin 2)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q35</field>
+ <field name="info">
+Pancreatitis, chronic, protection against</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRSS7">
+ <field name="name">PRSS7</field>
+ <field name="long_name">protease, serine, 7 (enterokinase)</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q21</field>
+ <field name="info">
+Enterokinase deficiency [MIM:226200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRS">
+ <field name="name">PRS</field>
+ <field name="long_name">Prieto X-linked mental retardation syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11-q21</field>
+ <field name="info">
+Mental retardation, X-linked, syndromic-2, with dysmorphism and cerebral atrophy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRTH">
+ <field name="name">PRTH</field>
+ <field name="long_name">pituitary resistance to thyroid hormone</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p24.3</field>
+ <field name="info">
+Thyroid hormone resistance [MIM:188570]
+Thyroid hormone resistance, autosomal recessive [MIM:274300]
+Thyroid hromone resistance, selective pituitary [MIM:145650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PRX">
+ <field name="name">PRX</field>
+ <field name="long_name">periaxin</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1-q13.2</field>
+ <field name="info">
+Dejerine-Sottas neuropathy, autosomal recessive [MIM:145900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSAP">
+ <field name="name">PSAP</field>
+ <field name="long_name">prosaposin</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.1</field>
+ <field name="info">
+Metachromatic leukodystrophy due to SAP-b deficiency [MIM:249900]
+Gaucher disease, atypical [MIM:610539]
+Combined SAP deficiency [MIM:611721]
+Krabbe disease, atypical [MIM:611722]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSAT1">
+ <field name="name">PSAT1</field>
+ <field name="long_name">phosphoserine aminotransferase 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q21.31</field>
+ <field name="info">
+Phosphoserine aminotransferase deficiency [MIM:610992]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSCA">
+ <field name="name">PSCA</field>
+ <field name="long_name">prostate stem cell antigen</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSEN1">
+ <field name="name">PSEN1</field>
+ <field name="long_name">presenilin 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3</field>
+ <field name="info">
+Alzheimer disease, type 3 [MIM:607822]
+Alzheimer disease, type 3, with spastic paraparesis and unusual plaques [MIM:607822]
+Alzheimer disease, type 3, with spastic paraparesis and apraxia [MIM:607822]
+Dementia, frontotemporal [MIM:600274]
+Pick disease [MIM:172700]
+Cardiomyopathy, dilated, 1U</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSEN2">
+ <field name="name">PSEN2</field>
+ <field name="long_name">presenilin 2 (Alzheimer disease 4)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31-q42</field>
+ <field name="info">
+Alzheimer disease-4 [MIM:606889]
+Cardiomyopathy, dilated, 1V</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSENEN">
+ <field name="name">PSENEN</field>
+ <field name="long_name">presenilin enhancer 2 homolog (C. elegans)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSHK2">
+ <field name="name">PSHK2</field>
+ <field name="long_name">Pseudohyperkalemia, familial, 2, due to red cell leak</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35-q36</field>
+ <field name="info">
+Pseudohyperkalemia, familial, 2, due to red cell leak</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSMA6">
+ <field name="name">PSMA6</field>
+ <field name="long_name">proteasome (prosome, macropain) subunit, alpha type, 6</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q13</field>
+ <field name="info">
+Myocardial infarcation, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSMB8">
+ <field name="name">PSMB8</field>
+ <field name="long_name">proteasome (prosome, macropain) subunit, beta type, 8 (large multifunctional peptidase 7)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSMB9">
+ <field name="name">PSMB9</field>
+ <field name="long_name">proteasome (prosome, macropain) subunit, beta type, 9 (large multifunctional peptidase 2)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSNP2">
+ <field name="name">PSNP2</field>
+ <field name="long_name">supranuclear palsy, progressive, 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31.1</field>
+ <field name="info">
+Supranuclear palsy, progressive, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSNP3">
+ <field name="name">PSNP3</field>
+ <field name="long_name">Supranuclear palsy, progressive, 3</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p12-p11</field>
+ <field name="info">
+Supranuclear palsy, progressive, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSORS10">
+ <field name="name">PSORS10</field>
+ <field name="long_name">psoriasis susceptibility 10</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.23</field>
+ <field name="info">
+Psoriasis susceptibility to [MIM:177900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSORS11">
+ <field name="name">PSORS11</field>
+ <field name="long_name">Psoriasis susceptibility 11</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1-q33.1</field>
+ <field name="info">
+Psoriasis susceptibility 11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSORS1">
+ <field name="name">PSORS1</field>
+ <field name="long_name">psoriasis susceptibility 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Psoriasis, early onset, susceptibility to [MIM:177900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSORS2">
+ <field name="name">PSORS2</field>
+ <field name="long_name">psoriasis susceptibility 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+Psoriasis, susceptibility to [MIM:177900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSORS3">
+ <field name="name">PSORS3</field>
+ <field name="long_name">psoriasis susceptibility 3</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q</field>
+ <field name="info">
+Psoriasis, susceptibility to [MIM:177900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSORS4">
+ <field name="name">PSORS4</field>
+ <field name="long_name">psoriasis susceptibility 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Psoriasis, susceptibility to [MIM:177900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSORS5">
+ <field name="name">PSORS5</field>
+ <field name="long_name">psoriasis susceptibility 5</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21</field>
+ <field name="info">
+Psoriasis, susceptibility to [MIM:177900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSORS6">
+ <field name="name">PSORS6</field>
+ <field name="long_name">psoriasis susceptibility 6</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13</field>
+ <field name="info">
+Psoriasis, susceptibility to [MIM:177900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSORS7">
+ <field name="name">PSORS7</field>
+ <field name="long_name">psoriasis susceptibility 7</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p</field>
+ <field name="info">
+Psoriasis, susceptibility to [MIM:177900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSORS8">
+ <field name="name">PSORS8</field>
+ <field name="long_name">psoriasis susceptibility 8</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q</field>
+ <field name="info">
+Psoriasis susceptibility 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSORS9">
+ <field name="name">PSORS9</field>
+ <field name="long_name">psoriasis susceptibility 9</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q31-q34</field>
+ <field name="info">
+Psoraisis, susceptibility to [MIM:177900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSS">
+ <field name="name">PSS</field>
+ <field name="long_name">Potocki-Shaffer syndrome</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p11.2</field>
+ <field name="info">
+Potocki-Shaffer syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PSTPIP1">
+ <field name="name">PSTPIP1</field>
+ <field name="long_name">proline-serine-threonine phosphatase interacting protein 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q24-q25.1</field>
+ <field name="info">
+Pyogenic sterile arthritis, pyoderma gangrenosum, and acne [MIM:604416]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTAFR">
+ <field name="name">PTAFR</field>
+ <field name="long_name">platelet-activating factor receptor</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p35-p34.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTCH1">
+ <field name="name">PTCH1</field>
+ <field name="long_name">patched homolog 1 (Drosophila)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22.3</field>
+ <field name="info">
+Basal cell nevus syndrome [MIM:109400]
+Basal cell carcinoma, somatic [MIM:605462]
+Holoprosencephaly-7 [MIM:610828]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTCH2">
+ <field name="name">PTCH2</field>
+ <field name="long_name">patched homolog 2 (Drosophila)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+Medulloblastoma [MIM:155255]
+Basal cell carcinoma, somatic [MIM:605462]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTCPRN">
+ <field name="name">PTCPRN</field>
+ <field name="long_name">Papillary thyroid carcinoma with papillary renal neoplasia</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Thyroid carcinoma, papillary, with papillary renal neoplasia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTEN">
+ <field name="name">PTEN</field>
+ <field name="long_name">phosphatase and tensin homolog</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23.31</field>
+ <field name="info">
+Cowden disease [MIM:158350]
+Lhermitte-Duclos syndrome
+Prostate cancer [MIM:176807]
+Endometrial carcinoma
+Thyroid carcinoma, follicular [MIM:188470]
+Bannayan-Riley-Ruvalcaba syndrome [MIM:153480]
+Oligodendroglioma [MIM:137800]
+Meningioma [MIM:607174]
+VATER association with hydrocephalus [MIM:276950]
+Proteus syndrome [MIM:176920]
+Macrocephaly/autism syndrome [MIM:605309]
+Juvenile polyposis syndrome, infantile form [MIM:174900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTF1A">
+ <field name="name">PTF1A</field>
+ <field name="long_name">pancreas specific transcription factor, 1a</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p12.3</field>
+ <field name="info">
+Diabetes mellitus, permanent neonatal, with cerebellar agenesis [MIM:609069]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTGDR">
+ <field name="name">PTGDR</field>
+ <field name="long_name">prostaglandin D2 receptor (DP)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q22.1</field>
+ <field name="info">
+Asthma, susceptibility to, 1 [MIM:607277]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTGDS">
+ <field name="name">PTGDS</field>
+ <field name="long_name">prostaglandin D2 synthase 21kDa (brain)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.2-q34.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTGER2">
+ <field name="name">PTGER2</field>
+ <field name="long_name">prostaglandin E receptor 2 (subtype EP2), 53kDa</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q22</field>
+ <field name="info">
+Asthma, aspirin-induced, susceptibility to [MIM:208550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTGER4">
+ <field name="name">PTGER4</field>
+ <field name="long_name">prostaglandin E receptor 4 (subtype EP4)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTGES2">
+ <field name="name">PTGES2</field>
+ <field name="long_name">prostaglandin E synthase 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTGIR">
+ <field name="name">PTGIR</field>
+ <field name="long_name">prostaglandin I2 (prostacyclin) receptor (IP)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTGIS">
+ <field name="name">PTGIS</field>
+ <field name="long_name">prostaglandin I2 (prostacyclin) synthase</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.11-q13.13</field>
+ <field name="info">
+Hypertension, essential [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTGS1">
+ <field name="name">PTGS1</field>
+ <field name="long_name">prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q32-q33.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTGS2">
+ <field name="name">PTGS2</field>
+ <field name="long_name">prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q25.2-q25.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTHLH">
+ <field name="name">PTHLH</field>
+ <field name="long_name">parathyroid hormone-like hormone</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p12.1-p11.2</field>
+ <field name="info">
+Humoral hypercalcemia of malignancy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTH">
+ <field name="name">PTH</field>
+ <field name="long_name">parathyroid hormone</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.3-p15.1</field>
+ <field name="info">
+Hypoparathyroidism, autosomal dominant [MIM:146200]
+Hypoparathyroidism, autosomal recessive [MIM:146200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTLAH">
+ <field name="name">PTLAH</field>
+ <field name="long_name">patella aplasia-hypoplasia</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+Patella aplasia or hypoplasia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTLS">
+ <field name="name">PTLS</field>
+ <field name="long_name">Potocki-Lupski syndrome</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+Potocki-Lupski syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTOS1">
+ <field name="name">PTOS1</field>
+ <field name="long_name">ptosis, congenital 1 (autosomal dominant)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34.1-p32</field>
+ <field name="info">
+Ptosis, hereditary congenital, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTOS2">
+ <field name="name">PTOS2</field>
+ <field name="long_name">Ptosis, hereditary congenital 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24-q27.1</field>
+ <field name="info">
+Ptosis, hereditary congenital 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTPN11">
+ <field name="name">PTPN11</field>
+ <field name="long_name">protein tyrosine phosphatase, non-receptor type 11</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.1</field>
+ <field name="info">
+Noonan syndrome 1 [MIM:163950]
+Leopard syndrome [MIM:151100]
+Leukemia, juvenile myelomonocytic [MIM:607785]
+Noonan-like/multiple giant cell lesion syndrome [MIM:163955]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTPN12">
+ <field name="name">PTPN12</field>
+ <field name="long_name">protein tyrosine phosphatase, non-receptor type 12</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.23</field>
+ <field name="info">
+Colon cancer</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTPN13">
+ <field name="name">PTPN13</field>
+ <field name="long_name">protein tyrosine phosphatase, non-receptor type 13 (APO-1/CD95 (Fas)-associated phosphatase)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTPN1">
+ <field name="name">PTPN1</field>
+ <field name="long_name">protein tyrosine phosphatase, non-receptor type 1</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.1-q13.2</field>
+ <field name="info">
+Insulin resistance, susceptibility to [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTPN22">
+ <field name="name">PTPN22</field>
+ <field name="long_name">protein tyrosine phosphatase, non-receptor type 22 (lymphoid)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13</field>
+ <field name="info">
+Diabetes, type 1, susceptibility to [MIM:222100]
+Rheumatoid arthritis, susceptibility to [MIM:180300]
+Systemic lupus erythematosus susceptibility to [MIM:152700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTPRB">
+ <field name="name">PTPRB</field>
+ <field name="long_name">protein tyrosine phosphatase, receptor type, B</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q15-q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTPRCAP">
+ <field name="name">PTPRCAP</field>
+ <field name="long_name">protein tyrosine phosphatase, receptor type, C-associated protein</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTPRC">
+ <field name="name">PTPRC</field>
+ <field name="long_name">protein tyrosine phosphatase, receptor type, C</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31-q32</field>
+ <field name="info">
+Multiple sclerosis, susceptibility to [MIM:126200]
+Hepatitic C virus, susceptibility to [MIM:609532]
+Severe combined immunodeficiency, T cell-negative, B-cell/natural killer-cell positive [MIM:608971]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTPRF">
+ <field name="name">PTPRF</field>
+ <field name="long_name">protein tyrosine phosphatase, receptor type, F</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTPRJ">
+ <field name="name">PTPRJ</field>
+ <field name="long_name">protein tyrosine phosphatase, receptor type, J</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p11.2</field>
+ <field name="info">
+Colon cancer, somatic [MIM:114500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTPRZ1">
+ <field name="name">PTPRZ1</field>
+ <field name="long_name">protein tyrosine phosphatase, receptor-type, Z polypeptide 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31.3</field>
+ <field name="info">
+H. pylori infection, susceptibility to [MIM:600263]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PTS">
+ <field name="name">PTS</field>
+ <field name="long_name">6-pyruvoyltetrahydropterin synthase</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22.3-q23.3</field>
+ <field name="info">
+Hyperphenylalaninemia, BH4-deficient, A [MIM:261640]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PUJO">
+ <field name="name">PUJO</field>
+ <field name="long_name">pelviureteric junction obstruction</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p</field>
+ <field name="info">
+Pelviureteric junction obstruction</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PUS1">
+ <field name="name">PUS1</field>
+ <field name="long_name">pseudouridylate synthase 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p16.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="PVRL1">
+ <field name="name">PVRL1</field>
+ <field name="long_name">poliovirus receptor-related 1 (herpesvirus entry mediator C)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23-q24</field>
+ <field name="info">
+Ectodermal dysplasia, Margarita Island type [MIM:225060]
+Zlotogora-Ogur syndrome [MIM:225000]
+Cleft lip/palate ectodermal dysplasia syndrome [MIM:225000]
+Orofacial cleft 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PVR">
+ <field name="name">PVR</field>
+ <field name="long_name">poliovirus receptor</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2-q13.3</field>
+ <field name="info">
+Polio, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PVT1">
+ <field name="name">PVT1</field>
+ <field name="long_name">Pvt1 oncogene (non-protein coding)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24</field>
+ <field name="info">
+Burkitt lymphoma variant/acute lymphoblastic leukemia with translocations t(2;8)(p12;q24);t(8;22)(q24;q11)</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PXMP3">
+ <field name="name">PXMP3</field>
+ <field name="long_name">peroxisomal membrane protein 3, 35kDa</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21.1</field>
+ <field name="info">
+Zellweger syndrome-3
+Refsum disease, infantile form [MIM:266510]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PYGL">
+ <field name="name">PYGL</field>
+ <field name="long_name">phosphorylase, glycogen, liver</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q21-q22</field>
+ <field name="info">
+Glycogen storage disease VI</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PYGM">
+ <field name="name">PYGM</field>
+ <field name="long_name">phosphorylase, glycogen, muscle</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+McArdle disease [MIM:232600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="PYY">
+ <field name="name">PYY</field>
+ <field name="long_name">peptide YY</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="QDPR">
+ <field name="name">QDPR</field>
+ <field name="long_name">quinoid dihydropteridine reductase</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15.31</field>
+ <field name="info">
+Hyperphenylalaninemia, BH4-deficient, C [MIM:261630]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAB23">
+ <field name="name">RAB23</field>
+ <field name="long_name">RAB23, member RAS oncogene family</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p11</field>
+ <field name="info">
+Carpenter syndrome [MIM:201000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAB27A">
+ <field name="name">RAB27A</field>
+ <field name="long_name">RAB27A, member RAS oncogene family</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21</field>
+ <field name="info">
+Griscelli syndrome, type 2 [MIM:607624]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAB3GAP1">
+ <field name="name">RAB3GAP1</field>
+ <field name="long_name">RAB3 GTPase activating protein subunit 1 (catalytic)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q21.3</field>
+ <field name="info">
+Warburg micro syndrome 1 [MIM:600118]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAB3GAP2">
+ <field name="name">RAB3GAP2</field>
+ <field name="long_name">RAB3 GTPase activating protein subunit 2 (non-catalytic)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q41</field>
+ <field name="info">
+Martsolf syndrome [MIM:212720]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAC2">
+ <field name="name">RAC2</field>
+ <field name="long_name">ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.3-q13.2</field>
+ <field name="info">
+Neutrophil immunodeficiency syndrome [MIM:608203]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAD23B">
+ <field name="name">RAD23B</field>
+ <field name="long_name">RAD23 homolog B (S. cerevisiae)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAD50">
+ <field name="name">RAD50</field>
+ <field name="long_name">RAD50 homolog (S. cerevisiae)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAD51L3">
+ <field name="name">RAD51L3</field>
+ <field name="long_name">RAD51-like 3 (S. cerevisiae)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAD51">
+ <field name="name">RAD51</field>
+ <field name="long_name">RAD51 homolog (RecA homolog, E. coli) (S. cerevisiae)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAD52">
+ <field name="name">RAD52</field>
+ <field name="long_name">RAD52 homolog (S. cerevisiae)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13-p12.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAD54B">
+ <field name="name">RAD54B</field>
+ <field name="long_name">RAD54 homolog B (S. cerevisiae)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21.3-q22</field>
+ <field name="info">
+Lymphoma, non-Hodgkin
+Colon adenocarcinoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAD54L">
+ <field name="name">RAD54L</field>
+ <field name="long_name">RAD54-like (S. cerevisiae)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+Lymphoma, non-Hodgkin
+Breast cancer, invasive intraductal
+Colon adenocarcinoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAD9A">
+ <field name="name">RAD9A</field>
+ <field name="long_name">RAD9 homolog A (S. pombe)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.1-q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAF1">
+ <field name="name">RAF1</field>
+ <field name="long_name">v-raf-1 murine leukemia viral oncogene homolog 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25</field>
+ <field name="info">
+Noonan syndrome 5 [MIM:611553]
+LEOPARD syndrome 2 [MIM:611554]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAG1">
+ <field name="name">RAG1</field>
+ <field name="long_name">recombination activating gene 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13</field>
+ <field name="info">
+Severe combined immunodeficiency, B cell-negative [MIM:601457]
+Omenn syndrome [MIM:603554]
+Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity [MIM:609889]
+Combined cellular and humoral immune defects with granulomas [MIM:233650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAG2">
+ <field name="name">RAG2</field>
+ <field name="long_name">recombination activating gene 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13</field>
+ <field name="info">
+Severe combined immunodeficiency, B cell-negative [MIM:601457]
+Omenn syndrome [MIM:603554]
+Combined cellular and humoral immune defects with granulomas [MIM:233650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAGE">
+ <field name="name">RAGE</field>
+ <field name="long_name">renal tumor antigen</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAI1">
+ <field name="name">RAI1</field>
+ <field name="long_name">retinoic acid induced 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+Smith-Magenis syndrome [MIM:182290]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RANBP2">
+ <field name="name">RANBP2</field>
+ <field name="long_name">RAN binding protein 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q11-q13</field>
+ <field name="info">
+Encephalopathy, acute necrotizing 1 [MIM:608033]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAN">
+ <field name="name">RAN</field>
+ <field name="long_name">RAN, member RAS oncogene family</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAP1GDS1">
+ <field name="name">RAP1GDS1</field>
+ <field name="long_name">RAP1, GTP-GDP dissociation stimulator 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21-q25</field>
+ <field name="info">
+Lymphocytic leukemia, acute T-cell</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAPSN">
+ <field name="name">RAPSN</field>
+ <field name="long_name">receptor-associated protein of the synapse</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p11.2-p11.1</field>
+ <field name="info">
+Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency [MIM:608931]
+Myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency [MIM:608931]
+Fetal akinesia deformation sequence [MIM:208150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RARA">
+ <field name="name">RARA</field>
+ <field name="long_name">retinoic acid receptor, alpha</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.1</field>
+ <field name="info">
+Leukemia, acute promyelocytic [MIM:612376]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RARS2">
+ <field name="name">RARS2</field>
+ <field name="long_name">arginyl-tRNA synthetase 2, mitochondrial</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q16.1</field>
+ <field name="info">
+Pontocerebellar hypoplasia, type 6 [MIM:611523]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RASA1">
+ <field name="name">RASA1</field>
+ <field name="long_name">RAS p21 protein activator (GTPase activating protein) 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13.3</field>
+ <field name="info">
+Basal cell carcinoma, somatic
+Parkes Weber syndrome [MIM:608355]
+Capillary malformation-arteriovenous malformation [MIM:608354]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RASSF1">
+ <field name="name">RASSF1</field>
+ <field name="long_name">Ras association (RalGDS/AF-6) domain family member 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.3</field>
+ <field name="info">
+Lung cancer [MIM:211980]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RAX">
+ <field name="name">RAX</field>
+ <field name="long_name">retina and anterior neural fold homeobox</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.3</field>
+ <field name="info">
+Microphthalmia, isolated 3 [MIM:611038]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RB1CC1">
+ <field name="name">RB1CC1</field>
+ <field name="long_name">RB1-inducible coiled-coil 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q11</field>
+ <field name="info">
+Breast cancer, somatic [MIM:114480]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RB1">
+ <field name="name">RB1</field>
+ <field name="long_name">retinoblastoma 1</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14.1-q14.2</field>
+ <field name="info">
+Retinoblastoma
+Osteosarcoma [MIM:259500]
+Bladder cancer [MIM:109800]
+Pinealoma with bilateral retinoblastoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RBBP8">
+ <field name="name">RBBP8</field>
+ <field name="long_name">retinoblastoma binding protein 8</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q11.2</field>
+ <field name="info">
+Pancreatic carcinoma, somatic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RBM15">
+ <field name="name">RBM15</field>
+ <field name="long_name">RNA binding motif protein 15</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13</field>
+ <field name="info">
+Megakaryoblastic leukemia, acute</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RBM28">
+ <field name="name">RBM28</field>
+ <field name="long_name">RNA binding motif protein 28</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q32.1</field>
+ <field name="info">
+Alopecia, neurologic defects, and endocrinopathy syndrome [MIM:612079]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RBMY1A1">
+ <field name="name">RBMY1A1</field>
+ <field name="long_name">RNA binding motif protein, Y-linked, family 1, member A1</field>
+ <field name="chromosome">Y</field>
+ <field name="location">Yq11</field>
+ <field name="info">
+Y Chromosome Infertility</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RBP4">
+ <field name="name">RBP4</field>
+ <field name="long_name">retinol binding protein 4, plasma</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+Retinol binding protein, deficiency of</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RCA1">
+ <field name="name">RCA1</field>
+ <field name="long_name">renal carcinoma, familial, associated 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.1</field>
+ <field name="info">
+Renal cell carcinoma [MIM:144700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RCC1">
+ <field name="name">RCC1</field>
+ <field name="long_name">regulator of chromosome condensation 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q13.1</field>
+ <field name="info">
+Skin/hair/eye pigmentation 1, blue/nonblue eyes [MIM:227220]
+Skin/hair/eye pigmentation 1, blond/brown hair [MIM:227220]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RCCP3">
+ <field name="name">RCCP3</field>
+ <field name="long_name">Renal cell carcinoma, papillary, 3</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.32</field>
+ <field name="info">
+Renal cell carcinoma, papillary, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RCD1">
+ <field name="name">RCD1</field>
+ <field name="long_name">retinal cone dystrophy 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25-q26</field>
+ <field name="info">
+Retinal cone dystrophy-1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RCD2">
+ <field name="name">RCD2</field>
+ <field name="long_name">Retinal cone dsytrophy 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p</field>
+ <field name="info">
+Retinal cone dystrophy 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RCM2">
+ <field name="name">RCM2</field>
+ <field name="long_name">cardiomyopathy, familial restrictive, 2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23.3</field>
+ <field name="info">
+Cardiomyopathy, familial restrictive, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RD3">
+ <field name="name">RD3</field>
+ <field name="long_name">retinal degeneration 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32.3</field>
+ <field name="info">
+Leber congenital amaurosis 12 [MIM:610612]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RDH12">
+ <field name="name">RDH12</field>
+ <field name="long_name">retinol dehydrogenase 12 (all-trans/9-cis/11-cis)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q23.3</field>
+ <field name="info">
+Leber congenital amaurosis 13 [MIM:612712]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RDH5">
+ <field name="name">RDH5</field>
+ <field name="long_name">retinol dehydrogenase 5 (11-cis/9-cis)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13-q14</field>
+ <field name="info">
+Fundus albipunctatus [MIM:136880]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RDPA">
+ <field name="name">RDPA</field>
+ <field name="long_name">refsum disease, adult, with increased pipecolicacidemia</field>
+ <field name="chromosome">10</field>
+ <field name="location">10pter-p11.2</field>
+ <field name="info">
+Refsum disease, adult, with increased pipecolicacidemia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RDX">
+ <field name="name">RDX</field>
+ <field name="long_name">radixin</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Deafness, autosomal recessive, 24 [MIM:611022]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RECQL4">
+ <field name="name">RECQL4</field>
+ <field name="long_name">RecQ protein-like 4</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.3</field>
+ <field name="info">
+Rothmund-Thomson syndrome [MIM:268400]
+RAPADILINO syndrome [MIM:266280]
+Baller-Gerold syndrome [MIM:218600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="REEP1">
+ <field name="name">REEP1</field>
+ <field name="long_name">receptor accessory protein 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p11.2</field>
+ <field name="info">
+Spastic paraplegia 31 [MIM:610250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RELN">
+ <field name="name">RELN</field>
+ <field name="long_name">reelin</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22</field>
+ <field name="info">
+Lissencephaly syndrome, Norman-Roberts type [MIM:257320]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="REL">
+ <field name="name">REL</field>
+ <field name="long_name">v-rel reticuloendotheliosis viral oncogene homolog (avian)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p13-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="REN">
+ <field name="name">REN</field>
+ <field name="long_name">renin</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+Hyperproreninemia
+Renal tubular dysgenesis [MIM:267430]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RETN">
+ <field name="name">RETN</field>
+ <field name="long_name">resistin</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent, susceptibility to [MIM:125853]
+Hypertension, insulin resistance-related, susceptibility to [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RET">
+ <field name="name">RET</field>
+ <field name="long_name">ret proto-oncogene</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q11.2</field>
+ <field name="info">
+Multiple endocrine neoplasia IIA [MIM:171400]
+Medullary thyroid carcinoma [MIM:155240]
+Multiple endocrine neoplasia IIB [MIM:162300]
+Hirschsprung disease [MIM:142623]
+Central hypoventilation syndrome, congenital [MIM:209880]
+Pheochromocytoma [MIM:171300]
+Renal agenesis [MIM:191830]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="REV3L">
+ <field name="name">REV3L</field>
+ <field name="long_name">REV3-like, catalytic subunit of DNA polymerase zeta (yeast)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RFC2">
+ <field name="name">RFC2</field>
+ <field name="long_name">replication factor C (activator 1) 2, 40kDa</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RFH1">
+ <field name="name">RFH1</field>
+ <field name="long_name">Renal failure, progressive, with hypertension</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Nephropathy-hypertension</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RFMN">
+ <field name="name">RFMN</field>
+ <field name="long_name">Roifman syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">X</field>
+ <field name="info">
+Roifman syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RFT1">
+ <field name="name">RFT1</field>
+ <field name="long_name">RFT1 homolog (S. cerevisiae)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.1</field>
+ <field name="info">
+Congenital disorder of glycosylation, type In [MIM:612015]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RFX1">
+ <field name="name">RFX1</field>
+ <field name="long_name">regulatory factor X, 1 (influences HLA class II expression)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.1</field>
+ <field name="info">
+immunodeficiency,severe combined with defective expression of MHC class II gene</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RFX5">
+ <field name="name">RFX5</field>
+ <field name="long_name">regulatory factor X, 5 (influences HLA class II expression)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21.1-q21.3</field>
+ <field name="info">
+Bare lymphocyte syndrome, type II, complementation group C [MIM:209920]
+Bare lymphocyte syndrome, type II, complementation group E [MIM:209920]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RFXANK">
+ <field name="name">RFXANK</field>
+ <field name="long_name">regulatory factor X-associated ankyrin-containing protein</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p12</field>
+ <field name="info">
+MHC class II deficiency, complementation group B [MIM:209920]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RFXAP">
+ <field name="name">RFXAP</field>
+ <field name="long_name">regulatory factor X-associated protein</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14</field>
+ <field name="info">
+Bare lymphocyte syndrome, type II, complementation group D [MIM:209920]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RGR">
+ <field name="name">RGR</field>
+ <field name="long_name">retinal G protein coupled receptor</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23</field>
+ <field name="info">
+Retinitis pigmentosa, autosomal recessive
+Retinitis pigmentosa, autosomal dominant</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RGS2">
+ <field name="name">RGS2</field>
+ <field name="long_name">regulator of G-protein signaling 2, 24kDa</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RGS5">
+ <field name="name">RGS5</field>
+ <field name="long_name">regulator of G-protein signaling 5</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23</field>
+ <field name="info">
+Blood pressure regulation QTL [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RGS6">
+ <field name="name">RGS6</field>
+ <field name="long_name">regulator of G-protein signaling 6</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RGS9BP">
+ <field name="name">RGS9BP</field>
+ <field name="long_name">regulator of G protein signaling 9 binding protein</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.11</field>
+ <field name="info">
+Bradyopsia [MIM:608415]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RGS9">
+ <field name="name">RGS9</field>
+ <field name="long_name">regulator of G-protein signaling 9</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23-q24</field>
+ <field name="info">
+Bradyopsia [MIM:608415]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RHAG">
+ <field name="name">RHAG</field>
+ <field name="long_name">Rh-associated glycoprotein</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.1-p11</field>
+ <field name="info">
+Anemia, hemolytic, Rh-null, regulator type [MIM:268150]
+Rh-mod syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RHCE">
+ <field name="name">RHCE</field>
+ <field name="long_name">Rh blood group, CcEe antigens</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2-p34</field>
+ <field name="info">
+Blood group, Rhesus
+Rh-null disease, amorph type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RHDNS1">
+ <field name="name">RHDNS1</field>
+ <field name="long_name">Renal hypodysplasia, nonsyndromic, 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p33-p32</field>
+ <field name="info">
+Renal hypodysplasia, nonsyndromic, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RHD">
+ <field name="name">RHD</field>
+ <field name="long_name">Rh blood group, D antigen</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2-p34</field>
+ <field name="info">
+Rh-negative blood type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RHO">
+ <field name="name">RHO</field>
+ <field name="long_name">rhodopsin</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21-q24</field>
+ <field name="info">
+Retinitis pigmentosa-4, autosomal dominant
+Retinitis pigmentosa, autosomal recessive
+Night blindness, congenital stationery, rhodopsin-related</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RIEG2">
+ <field name="name">RIEG2</field>
+ <field name="long_name">Rieger syndrome 2</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14</field>
+ <field name="info">
+Rieger syndrome, type 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RILP">
+ <field name="name">RILP</field>
+ <field name="long_name">Rab interacting lysosomal protein</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q12</field>
+ <field name="info">
+Epilepsy, progressive myoclonic 1B [MIM:612437]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RIMS1">
+ <field name="name">RIMS1</field>
+ <field name="long_name">regulating synaptic membrane exocytosis 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q12-q13</field>
+ <field name="info">
+Cone-rod dystrophy 7 [MIM:603649]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RIPK3">
+ <field name="name">RIPK3</field>
+ <field name="long_name">receptor-interacting serine-threonine kinase 3</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RLBP1">
+ <field name="name">RLBP1</field>
+ <field name="long_name">retinaldehyde binding protein 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26</field>
+ <field name="info">
+Fundus albipunctatus [MIM:136880]
+Retinitis punctata albescens [MIM:136880]
+Newfoundland rod-cone dystrophy [MIM:607476]
+Bothnia retinal dystrophy [MIM:607475]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RLS2">
+ <field name="name">RLS2</field>
+ <field name="long_name">Restless legs syndrome 2</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q13-q21</field>
+ <field name="info">
+Restless legs syndrome 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RLS3">
+ <field name="name">RLS3</field>
+ <field name="long_name">Restless legs syndrome 3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p24-p22</field>
+ <field name="info">
+Restless legs syndrome 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RLS4">
+ <field name="name">RLS4</field>
+ <field name="long_name">Restless legs syndrome 4</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33</field>
+ <field name="info">
+Restless legs syndrome 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RLS5">
+ <field name="name">RLS5</field>
+ <field name="long_name">Restless legs syndrome, susceptibility to, 5</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p13</field>
+ <field name="info">
+Restless legs syndrome, susceptibility to, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RMD1">
+ <field name="name">RMD1</field>
+ <field name="long_name">rippling muscle disease 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q41</field>
+ <field name="info">
+Rippling muscle disease-1 [MIM:606072]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RMRP">
+ <field name="name">RMRP</field>
+ <field name="long_name">RNA component of mitochondrial RNA processing endoribonuclease</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21-p12</field>
+ <field name="info">
+Cartilage-hair hypoplasia [MIM:250250]
+Metaphyseal dysplasia without hypotrichosis [MIM:250460]
+Anauxetic dysplasia [MIM:607095]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RNANC">
+ <field name="name">RNANC</field>
+ <field name="long_name">Retinal nonattachment, nonsyndromic congenital</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21</field>
+ <field name="info">
+Retinal nonattachment, nonsyndromic congenital</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RNASE3">
+ <field name="name">RNASE3</field>
+ <field name="long_name">ribonuclease, RNase A family, 3 (eosinophil cationic protein)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RNASEH2A">
+ <field name="name">RNASEH2A</field>
+ <field name="long_name">ribonuclease H2, subunit A</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.13</field>
+ <field name="info">
+Aicardi-Goutieres syndrome 4 [MIM:610333]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RNASEH2B">
+ <field name="name">RNASEH2B</field>
+ <field name="long_name">ribonuclease H2, subunit B</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14.1</field>
+ <field name="info">
+Aicardi-Goutieres syndrome 2 [MIM:610181]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RNASEH2C">
+ <field name="name">RNASEH2C</field>
+ <field name="long_name">ribonuclease H2, subunit C</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.2</field>
+ <field name="info">
+Aicardi-Goutieres syndrome 3 [MIM:610329]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RNASEL">
+ <field name="name">RNASEL</field>
+ <field name="long_name">ribonuclease L (2',5'-oligoisoadenylate synthetase-dependent)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q25</field>
+ <field name="info">
+Prostate cancer 1, 176807 [MIM:601518]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RNF135">
+ <field name="name">RNF135</field>
+ <field name="long_name">ring finger protein 135</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11</field>
+ <field name="info">
+Overgrowth syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RNF139">
+ <field name="name">RNF139</field>
+ <field name="long_name">ring finger protein 139</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.1</field>
+ <field name="info">
+Renal cell carcinoma [MIM:144700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RNF168">
+ <field name="name">RNF168</field>
+ <field name="long_name">ring finger protein 168</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q29</field>
+ <field name="info">
+RIDDLE syndrome [MIM:611943]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RNF212">
+ <field name="name">RNF212</field>
+ <field name="long_name">ring finger protein 212</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.3</field>
+ <field name="info">
+Recombination rate QTL 1 [MIM:612042]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RNF6">
+ <field name="name">RNF6</field>
+ <field name="long_name">ring finger protein (C3H2C3 type) 6</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12.11</field>
+ <field name="info">
+Esophageal carcinoma, somatic [MIM:133239]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ROBO1">
+ <field name="name">ROBO1</field>
+ <field name="long_name">roundabout, axon guidance receptor, homolog 1 (Drosophila)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ROBO2">
+ <field name="name">ROBO2</field>
+ <field name="long_name">roundabout, axon guidance receptor, homolog 2 (Drosophila)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p12.3</field>
+ <field name="info">
+Vesicoureteral reflux 2 [MIM:610878]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ROBO3">
+ <field name="name">ROBO3</field>
+ <field name="long_name">roundabout, axon guidance receptor, homolog 3 (Drosophila)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23-q25</field>
+ <field name="info">
+Gaze palsy, horizontal, with progressive scoliosis [MIM:607313]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ROCK1">
+ <field name="name">ROCK1</field>
+ <field name="long_name">Rho-associated, coiled-coil containing protein kinase 1</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q11.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ROM1">
+ <field name="name">ROM1</field>
+ <field name="long_name">retinal outer segment membrane protein 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Retinitis pigmentosa, digenic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ROR2">
+ <field name="name">ROR2</field>
+ <field name="long_name">receptor tyrosine kinase-like orphan receptor 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22</field>
+ <field name="info">
+Brachydactyly, type B1 [MIM:113000]
+Robinow syndrome, autosomal recessive [MIM:268310]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RORA">
+ <field name="name">RORA</field>
+ <field name="long_name">RAR-related orphan receptor A</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ROS1">
+ <field name="name">ROS1</field>
+ <field name="long_name">c-ros oncogene 1 , receptor tyrosine kinase</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RP1">
+ <field name="name">RP1</field>
+ <field name="long_name">retinitis pigmentosa 1 (autosomal dominant)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q11-q13</field>
+ <field name="info">
+Retinitis pigmentosa-1 [MIM:180100]
+Hypertriglyceridemia, susceptibility to [MIM:145750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RP22">
+ <field name="name">RP22</field>
+ <field name="long_name">retinitis pigmentosa 22 (autosomal recessive)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12.3-p12.1</field>
+ <field name="info">
+Retinitis pigmentosa-22</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RP23">
+ <field name="name">RP23</field>
+ <field name="long_name">retinitis pigmentosa 23 (X-linked recessive)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22</field>
+ <field name="info">
+Retinitis pigmentosa 23</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RP24">
+ <field name="name">RP24</field>
+ <field name="long_name">retinitis pigmentosa 24 (X-linked recessive)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26-q27</field>
+ <field name="info">
+Retinitis pigmentosa-24</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RP28">
+ <field name="name">RP28</field>
+ <field name="long_name">retinitis pigmentosa 28 (autosomal recessive)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p15-p11</field>
+ <field name="info">
+Retinitis pigmentosa-28</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RP29">
+ <field name="name">RP29</field>
+ <field name="long_name">retinitis pigmentosa 29 (autosomal recessive)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q32-q34</field>
+ <field name="info">
+Retinitis pigmentosa-29</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RP2">
+ <field name="name">RP2</field>
+ <field name="long_name">retinitis pigmentosa 2 (X-linked recessive)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.3</field>
+ <field name="info">
+Retinitis pigmentosa-2 [MIM:312600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RP32">
+ <field name="name">RP32</field>
+ <field name="long_name">retinitis pigmentosa 32 (autosomal recessive)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p21.3-p13.3</field>
+ <field name="info">
+Retinitis pigmentosa-32</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RP33">
+ <field name="name">RP33</field>
+ <field name="long_name">retinitis pigmentosa 33 (autosomal dominant)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q11.2</field>
+ <field name="info">
+Retinitis pigmentosa 33</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RP34">
+ <field name="name">RP34</field>
+ <field name="long_name">retinitis pigmentosa 34 (X-linked recessive)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Retinitis pigmentosa 34</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RP6">
+ <field name="name">RP6</field>
+ <field name="long_name">retinitis pigmentosa 6 (X-linked recessive)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp21.3-p21.2</field>
+ <field name="info">
+Retinitis pigmentosa-6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RP9">
+ <field name="name">RP9</field>
+ <field name="long_name">retinitis pigmentosa 9 (autosomal dominant)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14.2</field>
+ <field name="info">
+Retinitis pigmentosa-9 [MIM:180104]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPA1">
+ <field name="name">RPA1</field>
+ <field name="long_name">replication protein A1, 70kDa</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPA4">
+ <field name="name">RPA4</field>
+ <field name="long_name">replication protein A4, 34kDa</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq21.33</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPE65">
+ <field name="name">RPE65</field>
+ <field name="long_name">retinal pigment epithelium-specific protein 65kDa</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+Leber congenital amaurosis 2 [MIM:204100]
+Retinitis pigmentosa-20</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPGRIP1L">
+ <field name="name">RPGRIP1L</field>
+ <field name="long_name">RPGRIP1-like</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q12.2</field>
+ <field name="info">
+Joubert syndrome 7 [MIM:611560]
+Meckel syndrome, type 5 [MIM:611561]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPGRIP1">
+ <field name="name">RPGRIP1</field>
+ <field name="long_name">retinitis pigmentosa GTPase regulator interacting protein 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11</field>
+ <field name="info">
+Leber congenital amaurosis 6
+Cone-rod dystrophy 13 [MIM:608194]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPGR">
+ <field name="name">RPGR</field>
+ <field name="long_name">retinitis pigmentosa GTPase regulator</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp21.1</field>
+ <field name="info">
+Retinitis pigmentosa-3 [MIM:300389]
+Cone-rod dystrophy [MIM:300029]
+Cone dystrophy-1 [MIM:304020]
+Retinitis pigmentosa, X-linked, with recurrent respiratory infections [MIM:300455]
+Macular degeneration, X-linked atrophic
+Retinitis pigmentosa, X-linked with deafness and sinorespiratory infections [MIM:300455]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPH3AL">
+ <field name="name">RPH3AL</field>
+ <field name="long_name">rabphilin 3A-like (without C2 domains)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPIA">
+ <field name="name">RPIA</field>
+ <field name="long_name">ribose 5-phosphate isomerase A</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p11.2</field>
+ <field name="info">
+Ribose 5-phosphate isomerase deficiency [MIM:608611]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPL10">
+ <field name="name">RPL10</field>
+ <field name="long_name">ribosomal protein L10</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPL11">
+ <field name="name">RPL11</field>
+ <field name="long_name">ribosomal protein L11</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.1-p35</field>
+ <field name="info">
+Diamond-Blackfan anemia 7 [MIM:612562]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPL35A">
+ <field name="name">RPL35A</field>
+ <field name="long_name">ribosomal protein L35a</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q29-qter</field>
+ <field name="info">
+Diamond-Blackfan anemia 5 [MIM:612528]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPL5">
+ <field name="name">RPL5</field>
+ <field name="long_name">ribosomal protein L5</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p22.1</field>
+ <field name="info">
+Diamond-Blackfan anemia 6 [MIM:612561]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPS17">
+ <field name="name">RPS17</field>
+ <field name="long_name">ribosomal protein S17</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q</field>
+ <field name="info">
+Diamond-Blackfan anemia 4 [MIM:612527]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPS19">
+ <field name="name">RPS19</field>
+ <field name="long_name">ribosomal protein S19</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+Anemia, Diamond-Blackfan [MIM:105650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPS24">
+ <field name="name">RPS24</field>
+ <field name="long_name">ribosomal protein S24</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22-q23</field>
+ <field name="info">
+Diamond-blackfan anemia [MIM:610629]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPS6KA3">
+ <field name="name">RPS6KA3</field>
+ <field name="long_name">ribosomal protein S6 kinase, 90kDa, polypeptide 3</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.2-p22.1</field>
+ <field name="info">
+Coffin-Lowry syndrome [MIM:303600]
+Mental retardation, X-linked nonspecific, type 19</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPS7">
+ <field name="name">RPS7</field>
+ <field name="long_name">ribosomal protein S7</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p25</field>
+ <field name="info">
+Diamond-Blackfan anemia 8 [MIM:612563]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RPY">
+ <field name="name">RPY</field>
+ <field name="long_name">Retinitis pigmentosa, Y-linked</field>
+ <field name="chromosome">Y</field>
+ <field name="location">Y</field>
+ <field name="info">
+Retinitis pigmentosa, Y-linked</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RRAS2">
+ <field name="name">RRAS2</field>
+ <field name="long_name">related RAS viral (r-ras) oncogene homolog 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11pter-p15.5</field>
+ <field name="info">
+Ovarian carcinoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RRDX">
+ <field name="name">RRDX</field>
+ <field name="long_name">Radial ray deficiency</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24-q25</field>
+ <field name="info">
+Radial ray deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RRH">
+ <field name="name">RRH</field>
+ <field name="long_name">retinal pigment epithelium-derived rhodopsin homolog</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RRIS">
+ <field name="name">RRIS</field>
+ <field name="long_name">Respiratory rhythmicity in sleep</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q26</field>
+ <field name="info">
+Respiratory rhythmicity in sleep</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RRM2B">
+ <field name="name">RRM2B</field>
+ <field name="long_name">ribonucleotide reductase M2 B (TP53 inducible)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q23.1</field>
+ <field name="info">
+Mitochondrial DNA depletion syndrome, encephalomyopathic form, with renal tubulopathy [MIM:612075]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RS1">
+ <field name="name">RS1</field>
+ <field name="long_name">retinoschisin 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.2-p22.1</field>
+ <field name="info">
+Retinoschisis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RSCIS">
+ <field name="name">RSCIS</field>
+ <field name="long_name">Radiation sensitivity/chromosome instability syndrome, autosomal dominant</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2</field>
+ <field name="info">
+Radiation sensitivity/chromosome instability syndrome, autosomal dominant</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RSPH4A">
+ <field name="name">RSPH4A</field>
+ <field name="long_name">radial spoke head 4 homolog A (Chlamydomonas)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q22.1</field>
+ <field name="info">
+Ciliary dyskinesia, primary, 11 [MIM:612649]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RSPH9">
+ <field name="name">RSPH9</field>
+ <field name="long_name">radial spoke head 9 homolog (Chlamydomonas)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.1</field>
+ <field name="info">
+Ciliary dyskinesia, primary, 12 [MIM:612650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RSPO1">
+ <field name="name">RSPO1</field>
+ <field name="long_name">R-spondin homolog (Xenopus laevis)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34.3</field>
+ <field name="info">
+Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal [MIM:610644]
+Palmoplantar hyperkeratosis and true hermaphroditism [MIM:610644]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RSPO4">
+ <field name="name">RSPO4</field>
+ <field name="long_name">R-spondin family, member 4</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p13</field>
+ <field name="info">
+Anonychia congenita [MIM:206800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RSS">
+ <field name="name">RSS</field>
+ <field name="long_name">Russell Silver syndrome</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p11.2</field>
+ <field name="info">
+Silver-Russell syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RSTSS">
+ <field name="name">RSTSS</field>
+ <field name="long_name">Chromosome 16p13.3 deletion syndrome</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+Chromosome 16p13.3 deletion syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RTE1">
+ <field name="name">RTE1</field>
+ <field name="long_name">repressor of telomerase expression 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p15.1</field>
+ <field name="info">
+Glioma, high-grade [MIM:137800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RTF1">
+ <field name="name">RTF1</field>
+ <field name="long_name">Rtf1, Paf1/RNA polymerase II complex component, homolog (S. cerevisiae)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15.1</field>
+ <field name="info">
+Congenital disorder of glycosylation, type In [MIM:612015]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RTN4R">
+ <field name="name">RTN4R</field>
+ <field name="long_name">reticulon 4 receptor</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11</field>
+ <field name="info">
+Schizophrenia, susceptibility to [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RUNX1">
+ <field name="name">RUNX1</field>
+ <field name="long_name">runt-related transcription factor 1</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Leukemia, acute myeloid [MIM:601626]
+Platelet disorder, familial, with associated myeloid malignancy [MIM:601399]
+Rheumatoid arthritis, susceptibility to [MIM:180300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RUNX2">
+ <field name="name">RUNX2</field>
+ <field name="long_name">runt-related transcription factor 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21</field>
+ <field name="info">
+Cleidocranial dysplasia [MIM:119600]
+Dental anomalies, isolated</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RWS">
+ <field name="name">RWS</field>
+ <field name="long_name">Ragweed sensitivity</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Ragweed sensitivity</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RXRG">
+ <field name="name">RXRG</field>
+ <field name="long_name">retinoid X receptor, gamma</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q22-q23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="RYR1">
+ <field name="name">RYR1</field>
+ <field name="long_name">ryanodine receptor 1 (skeletal)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+Malignant hyperthermia susceptibility 1 [MIM:145600]
+Central core disease [MIM:117000]
+Minicore myopathy with external ophthalmoplegia [MIM:255320]
+Neuromuscular disease, congenital, with uniform type 1 fiber [MIM:117000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="RYR2">
+ <field name="name">RYR2</field>
+ <field name="long_name">ryanodine receptor 2 (cardiac)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42.1-q43</field>
+ <field name="info">
+Ventricular tachycardia, catecholaminergic polymorphic, 1 [MIM:604772]
+Arrhythmogenic right ventricular dysplasia 2 [MIM:600996]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SAA1">
+ <field name="name">SAA1</field>
+ <field name="long_name">serum amyloid A1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SACS">
+ <field name="name">SACS</field>
+ <field name="long_name">spastic ataxia of Charlevoix-Saguenay (sacsin)</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12</field>
+ <field name="info">
+Spastic ataxia, Charlevoix-Saguenay type [MIM:270550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SAG">
+ <field name="name">SAG</field>
+ <field name="long_name">S-antigen; retina and pineal gland (arrestin)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.1</field>
+ <field name="info">
+Oguchi disease-1 [MIM:258100]
+Retinitis pigmentosa-47</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SALL1">
+ <field name="name">SALL1</field>
+ <field name="long_name">sal-like 1 (Drosophila)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q12.1</field>
+ <field name="info">
+Townes-Brocks syndrome [MIM:107480]
+Townes-Brocks branchiootorenal-like syndrome [MIM:107480]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SALL4">
+ <field name="name">SALL4</field>
+ <field name="long_name">sal-like 4 (Drosophila)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.13-q13.2</field>
+ <field name="info">
+Duane-radial ray syndrome [MIM:607323]
+IVIC syndrome [MIM:147750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SAMD9">
+ <field name="name">SAMD9</field>
+ <field name="long_name">sterile alpha motif domain containing 9</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21</field>
+ <field name="info">
+Tumoral calcinosis, familial, normophosphatemic [MIM:610455]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SAR1B">
+ <field name="name">SAR1B</field>
+ <field name="long_name">SAR1 homolog B (S. cerevisiae)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1</field>
+ <field name="info">
+Chylomicron retention disease [MIM:246700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SARDH">
+ <field name="name">SARDH</field>
+ <field name="long_name">sarcosine dehydrogenase</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q33-q34</field>
+ <field name="info">
+Sarcosinemia [MIM:268900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SART1">
+ <field name="name">SART1</field>
+ <field name="long_name">squamous cell carcinoma antigen recognized by T cells</field>
+ <field name="chromosome">11</field>
+ <field name="location">11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SART3">
+ <field name="name">SART3</field>
+ <field name="long_name">squamous cell carcinoma antigen recognized by T cells 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.1</field>
+ <field name="info">
+Porokeratosis, disseminated superficial actinic, 1 [MIM:175900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SAT1">
+ <field name="name">SAT1</field>
+ <field name="long_name">spermidine/spermine N1-acetyltransferase 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.1</field>
+ <field name="info">
+Keratosis follicularis spinulosa decalvans [MIM:308800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SATB2">
+ <field name="name">SATB2</field>
+ <field name="long_name">SATB homeobox 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33</field>
+ <field name="info">
+Cleft palate and mental retardation [MIM:119540]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SATX2">
+ <field name="name">SATX2</field>
+ <field name="long_name">Ataxia, spastic 2, autosomal recessive</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13</field>
+ <field name="info">
+Ataxia, spastic 2, autosomal recessive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SBDS">
+ <field name="name">SBDS</field>
+ <field name="long_name">Shwachman-Bodian-Diamond syndrome</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11</field>
+ <field name="info">
+Shwachman-Bodian-Diamond syndrome [MIM:260400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SBF2">
+ <field name="name">SBF2</field>
+ <field name="long_name">SET binding factor 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 4B2 [MIM:604563]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SC5DL">
+ <field name="name">SC5DL</field>
+ <field name="long_name">sterol-C5-desaturase (ERG3 delta-5-desaturase homolog, S. cerevisiae)-like</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.3</field>
+ <field name="info">
+Lathosterolosis [MIM:607330]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCA18">
+ <field name="name">SCA18</field>
+ <field name="long_name">spinocerebellar ataxia 18 (sensory with neurogenic muscular atrophy)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22-q32</field>
+ <field name="info">
+Spinal cerebellar ataxia 18</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCA19">
+ <field name="name">SCA19</field>
+ <field name="long_name">spinocerebellar ataxia 19</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p21-q21</field>
+ <field name="info">
+Spinocerebellar ataxia 19</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCA20">
+ <field name="name">SCA20</field>
+ <field name="long_name">spinocerebellar ataxia 20</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13-q11</field>
+ <field name="info">
+Spinocerebellar ataxia 20</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCA23">
+ <field name="name">SCA23</field>
+ <field name="long_name">spinocerebellar ataxia 23</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p13-p12.3</field>
+ <field name="info">
+Spinocerebellar ataxia 23</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCA25">
+ <field name="name">SCA25</field>
+ <field name="long_name">spinocerebellar ataxia 25</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p21-p13</field>
+ <field name="info">
+Spinocerebellar ataxia 25</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCA28">
+ <field name="name">SCA28</field>
+ <field name="long_name">spinocerebellar ataxia 28</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.22-q11.2</field>
+ <field name="info">
+Spinocerebellar ataxia 28</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCA29">
+ <field name="name">SCA29</field>
+ <field name="long_name">spinocerebellar ataxia 29</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26</field>
+ <field name="info">
+Spinocerebellar ataxia 29</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCAP">
+ <field name="name">SCAP</field>
+ <field name="long_name">SREBF chaperone</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCAR2">
+ <field name="name">SCAR2</field>
+ <field name="long_name">spinocerebellar ataxia, autosomal recessive 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34-qter</field>
+ <field name="info">
+Spinocerebellar ataxia, autosomal recessive 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCAR3">
+ <field name="name">SCAR3</field>
+ <field name="long_name">spinocerebellar ataxia, autosomal recessive 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p23-p21</field>
+ <field name="info">
+Spinocerebellar ataxia, autosomal recessive 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCAR5">
+ <field name="name">SCAR5</field>
+ <field name="long_name">spinocerebellar ataxia, autosomal recessive 5</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q24-q26</field>
+ <field name="info">
+Spinocerebellar ataxia, autosomal recessive 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCAR6">
+ <field name="name">SCAR6</field>
+ <field name="long_name">spinocerebellar ataxia, autosomal recessive 6</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11-q13</field>
+ <field name="info">
+Spinocerebellar ataxia, autosomal recessive 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCAR7">
+ <field name="name">SCAR7</field>
+ <field name="long_name">spinocerebellar ataxia, autosomal recessive 7</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15</field>
+ <field name="info">
+Spinocerebellar ataxia, autosomal recessive 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCARB1">
+ <field name="name">SCARB1</field>
+ <field name="long_name">scavenger receptor class B, member 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCARB2">
+ <field name="name">SCARB2</field>
+ <field name="long_name">scavenger receptor class B, member 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q13-q21</field>
+ <field name="info">
+Action myoclonus-renal failure syndrome [MIM:254900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCASI">
+ <field name="name">SCASI</field>
+ <field name="long_name">spinocerebellar ataxia with saccadic intrusions</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Spinocerebellar ataxia, autosomal recessive 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCAX1">
+ <field name="name">SCAX1</field>
+ <field name="long_name">spinocerebellar ataxia, X-linked 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.21-q21.3</field>
+ <field name="info">
+Spinocerebellar ataxia, X-linked 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCAX5">
+ <field name="name">SCAX5</field>
+ <field name="long_name">Spinocerebellar ataxia, X-linked 5</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq25-q27.1</field>
+ <field name="info">
+Spinocerebellar ataxia, X-linked 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCCD">
+ <field name="name">SCCD</field>
+ <field name="long_name">Schnyder crystalline corneal dystrophy</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3</field>
+ <field name="info">
+Corneal dystrophy, crystalline, of Schnyder [MIM:121800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCG2">
+ <field name="name">SCG2</field>
+ <field name="long_name">secretogranin II (chromogranin C)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35-q36</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCG3">
+ <field name="name">SCG3</field>
+ <field name="long_name">secretogranin III</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCGB1A1">
+ <field name="name">SCGB1A1</field>
+ <field name="long_name">secretoglobin, family 1A, member 1 (uteroglobin)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q12.3-q13.1</field>
+ <field name="info">
+Asthma, susceptibility to [MIM:600807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCGB3A2">
+ <field name="name">SCGB3A2</field>
+ <field name="long_name">secretoglobin, family 3A, member 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31-q34</field>
+ <field name="info">
+Asthma, susceptibility to [MIM:600807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCKL2">
+ <field name="name">SCKL2</field>
+ <field name="long_name">Seckel syndrome 2</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.31-q11.2</field>
+ <field name="info">
+Seckel syndrome 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCKL3">
+ <field name="name">SCKL3</field>
+ <field name="long_name">Seckel syndrome 3</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q21-q22</field>
+ <field name="info">
+Seckel syndrome 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCLC1">
+ <field name="name">SCLC1</field>
+ <field name="long_name">small cell cancer of the lung</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p23-p21</field>
+ <field name="info">
+Small-cell cancer of lung</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCN1A">
+ <field name="name">SCN1A</field>
+ <field name="long_name">sodium channel, voltage-gated, type I, alpha subunit</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q24</field>
+ <field name="info">
+Epilepsy, generalized, with febrile seizures plus, type 2 [MIM:604233]
+Epilepsy, severe myoclonic, of infancy [MIM:607208]
+Migraine, familial hemiplegic, 3 [MIM:609634]
+Epilepsy, intractable childhood, with generalized tonic-clonic seizures [MIM:607208]
+Febrile convulsions, familial, 3 [MIM:604403]
+Antiepileptic drugs, response to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCN1B">
+ <field name="name">SCN1B</field>
+ <field name="long_name">sodium channel, voltage-gated, type I, beta</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+Generalized epilepsy with febrile seizures plus [MIM:604233]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCN2A">
+ <field name="name">SCN2A</field>
+ <field name="long_name">sodium channel, voltage-gated, type II, alpha subunit</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q23-q24.3</field>
+ <field name="info">
+Seizures, afebrile [MIM:604233]
+Seizures, benign familial neonatal-infantile [MIM:607745]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCN3A">
+ <field name="name">SCN3A</field>
+ <field name="long_name">sodium channel, voltage-gated, type III, alpha subunit</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCN4A">
+ <field name="name">SCN4A</field>
+ <field name="long_name">sodium channel, voltage-gated, type IV, alpha subunit</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23.1-q25.3</field>
+ <field name="info">
+Hyperkalemic periodic paralysis [MIM:170500]
+Paramyotonia congenita [MIM:168300]
+Myotonia congenita, atypical, acetazolamide-responsive [MIM:608390]
+Cramps, familial, potassium-aggravated
+Hypokalemic periodic paralysis [MIM:170400]
+Myasthenic syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCN4B">
+ <field name="name">SCN4B</field>
+ <field name="long_name">sodium channel, voltage-gated, type IV, beta</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Long QT syndrome-10 [MIM:611819]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCN5A">
+ <field name="name">SCN5A</field>
+ <field name="long_name">sodium channel, voltage-gated, type V, alpha subunit</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21</field>
+ <field name="info">
+Long QT syndrome-3 [MIM:603830]
+Brugada syndrome 1 [MIM:601144]
+Heart block, progressive, type IA [MIM:113900]
+Heart block, nonprogressive [MIM:113900]
+Ventricular fibrillation, idiopathic [MIM:603829]
+Sick sinus syndrome 1 [MIM:608567]
+Cardiomyopathy, dilated, 1E [MIM:601154]
+Sudden infant death syndrome, susceptibility to [MIM:272120]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCN8A">
+ <field name="name">SCN8A</field>
+ <field name="long_name">sodium channel, voltage gated, type VIII, alpha subunit</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCN9A">
+ <field name="name">SCN9A</field>
+ <field name="long_name">sodium channel, voltage-gated, type IX, alpha subunit</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q24</field>
+ <field name="info">
+Erythermalgia, primary [MIM:133020]
+Insensitivity to pain, channelopathy-associated [MIM:243000]
+Paroxysmal extreme pain disorder [MIM:167400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCNN1A">
+ <field name="name">SCNN1A</field>
+ <field name="long_name">sodium channel, nonvoltage-gated 1 alpha</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+Pseudohypoaldosteronism, type I [MIM:264350]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCNN1B">
+ <field name="name">SCNN1B</field>
+ <field name="long_name">sodium channel, nonvoltage-gated 1, beta</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13-p12</field>
+ <field name="info">
+Liddle syndrome [MIM:177200]
+Pseudohypoaldosteronism, type I [MIM:264350]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCNN1G">
+ <field name="name">SCNN1G</field>
+ <field name="long_name">sodium channel, nonvoltage-gated 1, gamma</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13-p12</field>
+ <field name="info">
+Liddle syndrome [MIM:177200]
+Pseudohypoaldosteronism, type I [MIM:264350]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCO1">
+ <field name="name">SCO1</field>
+ <field name="long_name">SCO cytochrome oxidase deficient homolog 1 (yeast)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13-p12</field>
+ <field name="info">
+Hepatic failure, early onset, and neurologic disorder</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCO2">
+ <field name="name">SCO2</field>
+ <field name="long_name">SCO cytochrome oxidase deficient homolog 2 (yeast)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13</field>
+ <field name="info">
+Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency [MIM:604377]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCP2">
+ <field name="name">SCP2</field>
+ <field name="long_name">sterol carrier protein 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+Leukoencephalopathy with dystonia and motor neuropathy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCRIB">
+ <field name="name">SCRIB</field>
+ <field name="long_name">scribbled homolog (Drosophila)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCT">
+ <field name="name">SCT</field>
+ <field name="long_name">secretin</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCZD10">
+ <field name="name">SCZD10</field>
+ <field name="long_name">schizophrenia disorder 10 (periodic catatonia)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCZD11">
+ <field name="name">SCZD11</field>
+ <field name="long_name">Schizophrenia susceptibility locus, chromosome 10q-related</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.3</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCZD12">
+ <field name="name">SCZD12</field>
+ <field name="long_name">schizophrenia 12</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2</field>
+ <field name="info">
+Schizophrenia 12 [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCZD13">
+ <field name="name">SCZD13</field>
+ <field name="long_name">Schizophrenia, susceptibility to, 13</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q32.1</field>
+ <field name="info">
+Schizophrenia, susceptibility to, 13</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCZD1">
+ <field name="name">SCZD1</field>
+ <field name="long_name">schizophrenia disorder 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q23-q35</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCZD2">
+ <field name="name">SCZD2</field>
+ <field name="long_name">schizophrenia disorder 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q14-q21</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCZD3">
+ <field name="name">SCZD3</field>
+ <field name="long_name">schizophrenia disorder 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p23</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCZD4">
+ <field name="name">SCZD4</field>
+ <field name="long_name">schizophrenia disorder 4</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+Hyperprolinemia, type I [MIM:239500]
+Schizophrenia, susceptibility to, 4 [MIM:600850]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCZD5">
+ <field name="name">SCZD5</field>
+ <field name="long_name">schizophrenia disorder 5</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q13-q26</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCZD6">
+ <field name="name">SCZD6</field>
+ <field name="long_name">schizophrenia disorder 6</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCZD7">
+ <field name="name">SCZD7</field>
+ <field name="long_name">schizophrenia disorder 7</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q32</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SCZD8">
+ <field name="name">SCZD8</field>
+ <field name="long_name">schizophrenia disorder 8</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p</field>
+ <field name="info">
+Schizophrenia [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SDC3">
+ <field name="name">SDC3</field>
+ <field name="long_name">syndecan 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1pter-p22.3</field>
+ <field name="info">
+Obesity, association with [MIM:601665]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SDHA">
+ <field name="name">SDHA</field>
+ <field name="long_name">succinate dehydrogenase complex, subunit A, flavoprotein (Fp)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15</field>
+ <field name="info">
+Leigh syndrome [MIM:256000]
+Mitochondrial respiratory chain complex II deficiency [MIM:252011]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SDHB">
+ <field name="name">SDHB</field>
+ <field name="long_name">succinate dehydrogenase complex, subunit B, iron sulfur (Ip)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.1-p35</field>
+ <field name="info">
+Paraganglioma, familial chromaffin, 4 [MIM:115310]
+Pheochromocytoma [MIM:171300]
+Paraganglioma and gastric stromal sarcoma [MIM:606864]
+Cowden-like syndrome [MIM:612359]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SDHC">
+ <field name="name">SDHC</field>
+ <field name="long_name">succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Paragangliomas, familial nonchromaffin, 3 [MIM:605373]
+Paraganglioma and gastric stromal sarcoma [MIM:606864]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SDHD">
+ <field name="name">SDHD</field>
+ <field name="long_name">succinate dehydrogenase complex, subunit D, integral membrane protein</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Paragangliomas, familial nonchromaffin, 1, with or without deafness [MIM:168000]
+Pheochromocytoma [MIM:171300]
+Carcinoid tumors, intestinal [MIM:114900]
+Merkel cell carcinoma, somatic
+Paraganglioma and gastric stromal sarcoma [MIM:606864]
+Cowden-like syndrome [MIM:612359]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SDS">
+ <field name="name">SDS</field>
+ <field name="long_name">serine dehydratase</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11</field>
+ <field name="info">
+Shwachman-Bodian-Diamond syndrome [MIM:260400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SDTY1">
+ <field name="name">SDTY1</field>
+ <field name="long_name">Syndactyly, type I</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q34-q36</field>
+ <field name="info">
+Syndactyly, type 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SEA">
+ <field name="name">SEA</field>
+ <field name="long_name">S13 erythroblastosis oncogene homolog (avian)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SEC23A">
+ <field name="name">SEC23A</field>
+ <field name="long_name">Sec23 homolog A (S. cerevisiae)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q21.1</field>
+ <field name="info">
+Craniolenticulosutural dysplasia [MIM:607812]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SEC63">
+ <field name="name">SEC63</field>
+ <field name="long_name">SEC63 homolog (S. cerevisiae)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+Polycystic liver disease [MIM:174050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SECISBP2">
+ <field name="name">SECISBP2</field>
+ <field name="long_name">SECIS binding protein 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22.2</field>
+ <field name="info">
+Thyroid hormone metabolism, abnormal [MIM:609698]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SEL1L">
+ <field name="name">SEL1L</field>
+ <field name="long_name">sel-1 suppressor of lin-12-like (C. elegans)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SELE">
+ <field name="name">SELE</field>
+ <field name="long_name">selectin E</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23-q25</field>
+ <field name="info">
+IgA nephropathy, susceptiblity to [MIM:161950]
+Atherosclerosis, susceptibility to
+Blood pressure regulation QTL [MIM:145500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SELL">
+ <field name="name">SELL</field>
+ <field name="long_name">selectin L</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23-q25</field>
+ <field name="info">
+IgA nephropathy susceptibility to [MIM:161950]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SELPLG">
+ <field name="name">SELPLG</field>
+ <field name="long_name">selectin P ligand</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SELP">
+ <field name="name">SELP</field>
+ <field name="long_name">selectin P (granule membrane protein 140kDa, antigen CD62)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23-q25</field>
+ <field name="info">
+Platelet alpha/delta storage pool deficiency
+Atopy, susceptibility to [MIM:147050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SELS">
+ <field name="name">SELS</field>
+ <field name="long_name">selenoprotein S</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26.3</field>
+ <field name="info">
+Inflammatory response, modulation of</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SEMA3E">
+ <field name="name">SEMA3E</field>
+ <field name="long_name">sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.11</field>
+ <field name="info">
+CHARGE syndrome [MIM:214800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SEMA4A">
+ <field name="name">SEMA4A</field>
+ <field name="long_name">sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q22</field>
+ <field name="info">
+Retinitis pigmentosa 35 [MIM:610282]
+Cone-rod dystrophy 10 [MIM:610283]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SEMA7A">
+ <field name="name">SEMA7A</field>
+ <field name="long_name">semaphorin 7A, GPI membrane anchor (John Milton Hagen blood group)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22.2-q23</field>
+ <field name="info">
+Blood group, John-Milton-Hagen</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SEMG1">
+ <field name="name">SEMG1</field>
+ <field name="long_name">semenogelin I</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q12-q13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SEN2">
+ <field name="name">SEN2</field>
+ <field name="long_name">senescence (cellular)-related 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25.1</field>
+ <field name="info">
+Pontocerebellar hypoplasia type 2B [MIM:612389]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="01/09/15">
+ <field name="name">01/09/15</field>
+ <field name="long_name">15 kDa selenoprotein</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SEPN1">
+ <field name="name">SEPN1</field>
+ <field name="long_name">selenoprotein N, 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36-p35</field>
+ <field name="info">
+Muscular dystrophy, rigid spine, 1 [MIM:602771]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SEPP1">
+ <field name="name">SEPP1</field>
+ <field name="long_name">selenoprotein P, plasma, 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SEPT9">
+ <field name="name">SEPT9</field>
+ <field name="long_name">septin 9</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+Leukemia, acute myeloid, therapy-related
+Ovarian carcinoma
+Amyotrophy, hereditary neuralgic [MIM:162100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SERPINA10">
+ <field name="name">SERPINA10</field>
+ <field name="long_name">serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 10</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.1</field>
+ <field name="info">
+Venous thrombosis, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SERPINA1">
+ <field name="name">SERPINA1</field>
+ <field name="long_name">serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.1</field>
+ <field name="info">
+Emphysema-cirrhosis
+Hemorrhagic diathesis due to \'antithrombin\' Pittsburgh
+Emphysema
+Pulmonary disease, chronic obstructive, susceptibility to [MIM:606963]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SERPINA3">
+ <field name="name">SERPINA3</field>
+ <field name="long_name">serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 3</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.1</field>
+ <field name="info">
+Alpha-1-antichymotrypsin deficiency
+Cerebrovascular disease, occlusive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SERPINA5">
+ <field name="name">SERPINA5</field>
+ <field name="long_name">serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 5</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.1</field>
+ <field name="info">
+Protein C inhibitor deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SERPINA6">
+ <field name="name">SERPINA6</field>
+ <field name="long_name">serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.1</field>
+ <field name="info">
+Corticosteroid-binding globulin deficiency [MIM:611489]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SERPINB5">
+ <field name="name">SERPINB5</field>
+ <field name="long_name">serpin peptidase inhibitor, clade B (ovalbumin), member 5</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SERPIND1">
+ <field name="name">SERPIND1</field>
+ <field name="long_name">serpin peptidase inhibitor, clade D (heparin cofactor), member 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11</field>
+ <field name="info">
+Thrombophilia due to heparin cofactor II deficiency [MIM:612356]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SERPINE1">
+ <field name="name">SERPINE1</field>
+ <field name="long_name">serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.3-q22</field>
+ <field name="info">
+Thrombophilia due to excessive plasminogen activator inhibitor
+Hemorrhagic diathesis due to PAI1 deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SERPINF1">
+ <field name="name">SERPINF1</field>
+ <field name="long_name">serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SERPINF2">
+ <field name="name">SERPINF2</field>
+ <field name="long_name">serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17pter-p12</field>
+ <field name="info">
+Plasmin inhibitor deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SERPING1">
+ <field name="name">SERPING1</field>
+ <field name="long_name">serpin peptidase inhibitor, clade G (C1 inhibitor), member 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q11-q13.1</field>
+ <field name="info">
+Angioedema, hereditary, types I and II [MIM:106100]
+Complement component 4, partial deficiency of [MIM:120790]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SERPINI1">
+ <field name="name">SERPINI1</field>
+ <field name="long_name">serpin peptidase inhibitor, clade I (neuroserpin), member 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26</field>
+ <field name="info">
+Encephalopathy, familial, with neuroserpin inclusion bodies [MIM:604218]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SETBP1">
+ <field name="name">SETBP1</field>
+ <field name="long_name">SET binding protein 1</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.1</field>
+ <field name="info">
+Leukemia, acute T-cell lymphoblastic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SETDB2">
+ <field name="name">SETDB2</field>
+ <field name="long_name">SET domain, bifurcated 2</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SETX">
+ <field name="name">SETX</field>
+ <field name="long_name">senataxin</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+Ataxia-ocular apraxia-2 [MIM:606002]
+Amyotrophic lateral sclerosis 4, juvenile [MIM:602433]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SET">
+ <field name="name">SET</field>
+ <field name="long_name">SET nuclear oncogene</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+acute undifferentiated leukemia (AUL);see also CAN</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SFRS2IP">
+ <field name="name">SFRS2IP</field>
+ <field name="long_name">splicing factor, arginine/serine-rich 2, interacting protein</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SFTPA1">
+ <field name="name">SFTPA1</field>
+ <field name="long_name">surfactant protein A1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.2-q23.1</field>
+ <field name="info">
+Pulmonary fibrosis, idiopathic, susceptibility to [MIM:178500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SFTPA2">
+ <field name="name">SFTPA2</field>
+ <field name="long_name">surfactant protein A2</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22-q23</field>
+ <field name="info">
+Pulmonary fibrosis, idiopathic [MIM:178500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SFTPB">
+ <field name="name">SFTPB</field>
+ <field name="long_name">surfactant protein B</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p12-p11.2</field>
+ <field name="info">
+Surfactant metabolism dysfunction, pulmonary, 1 [MIM:265120]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SFTPC">
+ <field name="name">SFTPC</field>
+ <field name="long_name">surfactant protein C</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21</field>
+ <field name="info">
+Surfactant metabolism dysfunction, pulmonary, 2 [MIM:610913]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SFTPD">
+ <field name="name">SFTPD</field>
+ <field name="long_name">surfactant protein D</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SF">
+ <field name="name">SF</field>
+ <field name="long_name">Stoltzfus blood group</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q28-q31</field>
+ <field name="info">
+Blood group, Stoltzfus system</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SGCA">
+ <field name="name">SGCA</field>
+ <field name="long_name">sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12-q21.33</field>
+ <field name="info">
+Muscular dystrophy, limb-girdle, type 2D [MIM:608099]
+Adhalinopathy, primary</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SGCB">
+ <field name="name">SGCB</field>
+ <field name="long_name">sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q12</field>
+ <field name="info">
+Muscular dystrophy, limb-girdle, type 2E [MIM:604286]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SGCD">
+ <field name="name">SGCD</field>
+ <field name="long_name">sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q33</field>
+ <field name="info">
+Muscular dystrophy, limb-girdle, type 2F [MIM:601287]
+Cardiomyopathy, dilated, 1L [MIM:606685]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SGCE">
+ <field name="name">SGCE</field>
+ <field name="long_name">sarcoglycan, epsilon</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21</field>
+ <field name="info">
+Dystonia-11, myoclonic [MIM:159900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SGCG">
+ <field name="name">SGCG</field>
+ <field name="long_name">sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12</field>
+ <field name="info">
+Muscular dystrophy, limb-girdle, type 2C [MIM:253700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SGM1">
+ <field name="name">SGM1</field>
+ <field name="long_name">segmentation syndrome 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q22.2</field>
+ <field name="info">
+Klippel-Feil syndrome with laryngeal malformation</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SGSH">
+ <field name="name">SGSH</field>
+ <field name="long_name">N-sulfoglucosamine sulfohydrolase</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25.3</field>
+ <field name="info">
+Sanfilippo syndrome, type A [MIM:252900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SH2B3">
+ <field name="name">SH2B3</field>
+ <field name="long_name">SH2B adaptor protein 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SH2D1A">
+ <field name="name">SH2D1A</field>
+ <field name="long_name">SH2 domain protein 1A</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq25</field>
+ <field name="info">
+Lymphoproliferative syndrome, X-linked [MIM:308240]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SH3BP2">
+ <field name="name">SH3BP2</field>
+ <field name="long_name">SH3-domain binding protein 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.3</field>
+ <field name="info">
+Cherubism [MIM:118400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SH3GL1">
+ <field name="name">SH3GL1</field>
+ <field name="long_name">SH3-domain GRB2-like 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Leukemia, acute myeloid [MIM:601626]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SH3TC2">
+ <field name="name">SH3TC2</field>
+ <field name="long_name">SH3 domain and tetratricopeptide repeats 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q32</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 4C [MIM:601596]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHANK3">
+ <field name="name">SHANK3</field>
+ <field name="long_name">SH3 and multiple ankyrin repeat domains 3</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.3</field>
+ <field name="info">
+Chromosome 22q13.3 deletion syndrome [MIM:606232]
+Autism, chromosome 22q13.3 deletion syndrome-related</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHBG">
+ <field name="name">SHBG</field>
+ <field name="long_name">sex hormone-binding globulin</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHEP11">
+ <field name="name">SHEP11</field>
+ <field name="long_name">Skin/hair/eye pigmentation 11, blue/nonblue eyes</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p23</field>
+ <field name="info">
+Skin/hair/eye pigmentation 11, blue/nonblue eyes</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHEP8">
+ <field name="name">SHEP8</field>
+ <field name="long_name">Skin/hair/eye pigmentation 8, freckling</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p25.3</field>
+ <field name="info">
+Skin/hair/eye pigmentation 8, freckling</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHFL1">
+ <field name="name">SHFL1</field>
+ <field name="long_name">Split-hand/foot malformation with long bone deficiency 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42.2-q43</field>
+ <field name="info">
+Split-hand/foot malformation with long bone deficiency 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHFLD2">
+ <field name="name">SHFLD2</field>
+ <field name="long_name">Split-hand/foot malformation with long deficiency 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q14.1</field>
+ <field name="info">
+Split-hand/foot malformation with long deficiency 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHFLD3">
+ <field name="name">SHFLD3</field>
+ <field name="long_name">Split-hand/foot malformation with long bone deficiency 3</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.3-p13.1</field>
+ <field name="info">
+Split-hand/foot malformation with long bone deficiency 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHFM1D">
+ <field name="name">SHFM1D</field>
+ <field name="long_name">Split hand/foot malformation type 1 with sensorineural hearing loss</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.2-q21.3</field>
+ <field name="info">
+Split hand/foot malformation type 1 with deafness</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHFM1">
+ <field name="name">SHFM1</field>
+ <field name="long_name">split hand/foot malformation (ectrodactyly) type 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.2-q21.3</field>
+ <field name="info">
+Split hand/foot malformation, type 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHFM2">
+ <field name="name">SHFM2</field>
+ <field name="long_name">split hand/foot malformation (ectrodactyly) type 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26</field>
+ <field name="info">
+Split hand/foot malformation, type 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHFM3">
+ <field name="name">SHFM3</field>
+ <field name="long_name">Split-hand/foot malformation 3</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+Split-hand/foot malformation 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHFM5">
+ <field name="name">SHFM5</field>
+ <field name="long_name">split hand/foot malformation (ectrodactyly) type 5</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31</field>
+ <field name="info">
+Split-hand/foot malformation 5 [MIM:183600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHH">
+ <field name="name">SHH</field>
+ <field name="long_name">sonic hedgehog homolog (Drosophila)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q36</field>
+ <field name="info">
+Holoprosencephaly-3 [MIM:142945]
+Solitary median maxillary central incisor [MIM:147250]
+Coloboma, ocular [MIM:120200]
+Microphthalmia, isolated, with coloboma 5 [MIM:611638]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHMT1">
+ <field name="name">SHMT1</field>
+ <field name="long_name">serine hydroxymethyltransferase 1 (soluble)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHOX">
+ <field name="name">SHOX</field>
+ <field name="long_name">short stature homeobox</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xpter-p22.32</field>
+ <field name="info">
+Short stature, idiopathic familial [MIM:300582]
+Leri-Weill dyschondrosteosis [MIM:127300]
+Langer mesomelic dysplasia [MIM:249700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHROOM3">
+ <field name="name">SHROOM3</field>
+ <field name="long_name">shroom family member 3</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SHROOM4">
+ <field name="name">SHROOM4</field>
+ <field name="long_name">shroom family member 4</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.2</field>
+ <field name="info">
+Stocco dos Santos X-linked mental retardation syndrome [MIM:300434]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SIL1">
+ <field name="name">SIL1</field>
+ <field name="long_name">SIL1 homolog, endoplasmic reticulum chaperone (S. cerevisiae)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Marinesco-Sjogren syndrome [MIM:248800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SIM1">
+ <field name="name">SIM1</field>
+ <field name="long_name">single-minded homolog 1 (Drosophila)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q16.3-q21</field>
+ <field name="info">
+Obesity, severe [MIM:601665]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SIPA1">
+ <field name="name">SIPA1</field>
+ <field name="long_name">signal-induced proliferation-associated 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.3</field>
+ <field name="info">
+Metastasis efficiency, modification of</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SIRT3">
+ <field name="name">SIRT3</field>
+ <field name="long_name">sirtuin (silent mating type information regulation 2 homolog) 3 (S. cerevisiae)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SIX1">
+ <field name="name">SIX1</field>
+ <field name="long_name">SIX homeobox 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q23</field>
+ <field name="info">
+Brachiootic syndrome 3 [MIM:608389]
+Deafness, autosomal dominant 23 [MIM:605192]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SIX2">
+ <field name="name">SIX2</field>
+ <field name="long_name">SIX homeobox 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p16-p15</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SIX3">
+ <field name="name">SIX3</field>
+ <field name="long_name">SIX homeobox 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p21</field>
+ <field name="info">
+Holoprosencephaly-2 [MIM:157170]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SIX5">
+ <field name="name">SIX5</field>
+ <field name="long_name">SIX homeobox 5</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+Branchiootorenal syndrome 2 [MIM:610896]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SIX6">
+ <field name="name">SIX6</field>
+ <field name="long_name">SIX homeobox 6</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q23</field>
+ <field name="info">
+Microphthalmia, isolated, with cataract 2 [MIM:212550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SI">
+ <field name="name">SI</field>
+ <field name="long_name">sucrase-isomaltase (alpha-glucosidase)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q25-q26</field>
+ <field name="info">
+Sucrase-isomaltase deficiency, congenital [MIM:222900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SKI">
+ <field name="name">SKI</field>
+ <field name="long_name">v-ski sarcoma viral oncogene homolog (avian)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3</field>
+ <field name="info">
+1p36 deletion syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC10A2">
+ <field name="name">SLC10A2</field>
+ <field name="long_name">solute carrier family 10 (sodium/bile acid cotransporter family), member 2</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q33</field>
+ <field name="info">
+Bile acid malabsorption, primary</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC12A1">
+ <field name="name">SLC12A1</field>
+ <field name="long_name">solute carrier family 12 (sodium/potassium/chloride transporters), member 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15-q21.1</field>
+ <field name="info">
+Bartter syndrome, type 1 [MIM:601678]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC12A3">
+ <field name="name">SLC12A3</field>
+ <field name="long_name">solute carrier family 12 (sodium/chloride transporters), member 3</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q13</field>
+ <field name="info">
+Gitelman syndrome [MIM:263800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC12A6">
+ <field name="name">SLC12A6</field>
+ <field name="long_name">solute carrier family 12 (potassium/chloride transporters), member 6</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q13-q14</field>
+ <field name="info">
+Agenesis of the corpus callosum with peripheral neuropathy [MIM:218000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC14A1">
+ <field name="name">SLC14A1</field>
+ <field name="long_name">solute carrier family 14 (urea transporter), member 1 (Kidd blood group)</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q11-q12</field>
+ <field name="info">
+Urea transport defect, compensated
+Blood group, Kidd</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC14A2">
+ <field name="name">SLC14A2</field>
+ <field name="long_name">solute carrier family 14 (urea transporter), member 2</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q12.1-q21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC15A1">
+ <field name="name">SLC15A1</field>
+ <field name="long_name">solute carrier family 15 (oligopeptide transporter), member 1</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q33-q34</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC16A12">
+ <field name="name">SLC16A12</field>
+ <field name="long_name">solute carrier family 16, member 12 (monocarboxylic acid transporter 12)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23.3</field>
+ <field name="info">
+Cataract, juvenile, with microcornea and glucosuria [MIM:612018]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC16A1">
+ <field name="name">SLC16A1</field>
+ <field name="long_name">solute carrier family 16, member 1 (monocarboxylic acid transporter 1)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13.2-p12</field>
+ <field name="info">
+Erythrocyte lactate transporter defect [MIM:245340]
+Hyperinsulinemic hypoglycemia, familial, 7 [MIM:610021]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC16A2">
+ <field name="name">SLC16A2</field>
+ <field name="long_name">solute carrier family 16, member 2 (monocarboxylic acid transporter 8)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.2</field>
+ <field name="info">
+Allan-Herndon-Dudley syndrome [MIM:300523]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC17A1">
+ <field name="name">SLC17A1</field>
+ <field name="long_name">solute carrier family 17 (sodium phosphate), member 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p23-p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC17A3">
+ <field name="name">SLC17A3</field>
+ <field name="long_name">solute carrier family 17 (sodium phosphate), member 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Glycogen storage disease Ic [MIM:232240]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC17A5">
+ <field name="name">SLC17A5</field>
+ <field name="long_name">solute carrier family 17 (anion/sugar transporter), member 5</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q14-q15</field>
+ <field name="info">
+Salla disease [MIM:604369]
+Sialic acid storage disorder, infantile [MIM:269920]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC17A8">
+ <field name="name">SLC17A8</field>
+ <field name="long_name">solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q23</field>
+ <field name="info">
+Deafness, autosomal dominant 25 [MIM:605583]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC18A1">
+ <field name="name">SLC18A1</field>
+ <field name="long_name">solute carrier family 18 (vesicular monoamine), member 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC19A1">
+ <field name="name">SLC19A1</field>
+ <field name="long_name">solute carrier family 19 (folate transporter), member 1</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC19A2">
+ <field name="name">SLC19A2</field>
+ <field name="long_name">solute carrier family 19 (thiamine transporter), member 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q23.3</field>
+ <field name="info">
+Thiamine-responsive megaloblastic anemia syndrome [MIM:249270]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC19A3">
+ <field name="name">SLC19A3</field>
+ <field name="long_name">solute carrier family 19, member 3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q36.3</field>
+ <field name="info">
+Basal ganglia disease, biotin-responsive [MIM:607483]
+Encephalopathy, thiamine-responsive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC1A1">
+ <field name="name">SLC1A1</field>
+ <field name="long_name">solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p24</field>
+ <field name="info">
+Dicarboxylicaminoaciduria [MIM:222730]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC1A2">
+ <field name="name">SLC1A2</field>
+ <field name="long_name">solute carrier family 1 (glial high affinity glutamate transporter), member 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC1A3">
+ <field name="name">SLC1A3</field>
+ <field name="long_name">solute carrier family 1 (glial high affinity glutamate transporter), member 3</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13</field>
+ <field name="info">
+Episodic ataxia, type 6 [MIM:612656]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC22A11">
+ <field name="name">SLC22A11</field>
+ <field name="long_name">solute carrier family 22 (organic anion/urate transporter), member 11</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC22A12">
+ <field name="name">SLC22A12</field>
+ <field name="long_name">solute carrier family 22 (organic anion/urate transporter), member 12</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Hypouricemia, renal [MIM:220150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC22A1">
+ <field name="name">SLC22A1</field>
+ <field name="long_name">solute carrier family 22 (organic cation transporter), member 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q26</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC22A2">
+ <field name="name">SLC22A2</field>
+ <field name="long_name">solute carrier family 22 (organic cation transporter), member 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q26</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC22A3">
+ <field name="name">SLC22A3</field>
+ <field name="long_name">solute carrier family 22 (extraneuronal monoamine transporter), member 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q27</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC22A4">
+ <field name="name">SLC22A4</field>
+ <field name="long_name">solute carrier family 22 (organic cation/ergothioneine transporter), member 4</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Rheumatoid arthritis, susceptibility to [MIM:180300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC22A5">
+ <field name="name">SLC22A5</field>
+ <field name="long_name">solute carrier family 22 (organic cation/carnitine transporter), member 5</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1</field>
+ <field name="info">
+Carnitine deficiency, systemic primary [MIM:212140]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC22A6">
+ <field name="name">SLC22A6</field>
+ <field name="long_name">solute carrier family 22 (organic anion transporter), member 6</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.1-q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC24A1">
+ <field name="name">SLC24A1</field>
+ <field name="long_name">solute carrier family 24 (sodium/potassium/calcium exchanger), member 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC24A2">
+ <field name="name">SLC24A2</field>
+ <field name="long_name">solute carrier family 24 (sodium/potassium/calcium exchanger), member 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC24A5">
+ <field name="name">SLC24A5</field>
+ <field name="long_name">solute carrier family 24, member 5</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21.1</field>
+ <field name="info">
+Skin/hair/eye pigmentation 4, fair/dark skin [MIM:113750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC25A13">
+ <field name="name">SLC25A13</field>
+ <field name="long_name">solute carrier family 25, member 13 (citrin)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.3</field>
+ <field name="info">
+Citrullinemia, adult-onset type II [MIM:603471]
+Citrullinemia, type II, neonatal-onset [MIM:605814]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC25A15">
+ <field name="name">SLC25A15</field>
+ <field name="long_name">solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14</field>
+ <field name="info">
+Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome [MIM:238970]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC25A19">
+ <field name="name">SLC25A19</field>
+ <field name="long_name">solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25.3</field>
+ <field name="info">
+Microcephaly, Amish type [MIM:607196]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC25A20">
+ <field name="name">SLC25A20</field>
+ <field name="long_name">solute carrier family 25 (carnitine/acylcarnitine translocase), member 20</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.31</field>
+ <field name="info">
+Carnitine-acylcarnitine translocase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC25A22">
+ <field name="name">SLC25A22</field>
+ <field name="long_name">solute carrier family 25 (mitochondrial carrier: glutamate), member 22</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Epilepsy, neonatal myoclonic, with suppression-burst pattern [MIM:609304]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC25A3">
+ <field name="name">SLC25A3</field>
+ <field name="long_name">solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q23</field>
+ <field name="info">
+Micochondrial phosphate carrier deficiency [MIM:610773]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC25A4">
+ <field name="name">SLC25A4</field>
+ <field name="long_name">solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q35</field>
+ <field name="info">
+Progressive external ophthalmoplegia with mitochondrial DNA deletions [MIM:157640]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC26A2">
+ <field name="name">SLC26A2</field>
+ <field name="long_name">solute carrier family 26 (sulfate transporter), member 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q32-q33.1</field>
+ <field name="info">
+Diastrophic dysplasia [MIM:222600]
+Atelosteogenesis II [MIM:256050]
+Achondrogenesis Ib [MIM:600972]
+Epiphyseal dysplasia, multiple, 4 [MIM:226900]
+Diastrophic dysplasia, broad bone-platyspondylic variant [MIM:222600]
+De la Chapelle dysplasia [MIM:256050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC26A3">
+ <field name="name">SLC26A3</field>
+ <field name="long_name">solute carrier family 26, member 3</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22-q31.1</field>
+ <field name="info">
+Colon cancer
+Chloride diarrhea, congenital, Finnish type [MIM:214700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC26A4">
+ <field name="name">SLC26A4</field>
+ <field name="long_name">solute carrier family 26, member 4</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31</field>
+ <field name="info">
+Pendred syndrome [MIM:274600]
+Enlarged vestibular aqueduct [MIM:600791]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC26A5">
+ <field name="name">SLC26A5</field>
+ <field name="long_name">solute carrier family 26, member 5 (prestin)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22.1</field>
+ <field name="info">
+Deafness, autosomal recessive 61</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC26A6">
+ <field name="name">SLC26A6</field>
+ <field name="long_name">solute carrier family 26, member 6</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC27A4">
+ <field name="name">SLC27A4</field>
+ <field name="long_name">solute carrier family 27 (fatty acid transporter), member 4</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC28A1">
+ <field name="name">SLC28A1</field>
+ <field name="long_name">solute carrier family 28 (sodium-coupled nucleoside transporter), member 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q25-q26</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC28A2">
+ <field name="name">SLC28A2</field>
+ <field name="long_name">solute carrier family 28 (sodium-coupled nucleoside transporter), member 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC28A3">
+ <field name="name">SLC28A3</field>
+ <field name="long_name">solute carrier family 28 (sodium-coupled nucleoside transporter), member 3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC29A1">
+ <field name="name">SLC29A1</field>
+ <field name="long_name">solute carrier family 29 (nucleoside transporters), member 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.2-p21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC29A2">
+ <field name="name">SLC29A2</field>
+ <field name="long_name">solute carrier family 29 (nucleoside transporters), member 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC29A3">
+ <field name="name">SLC29A3</field>
+ <field name="long_name">solute carrier family 29 (nucleoside transporters), member 3</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.1</field>
+ <field name="info">
+Hyperpigmentation, cutaneous, with hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, and hypogonadism [MIM:612391]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC2A10">
+ <field name="name">SLC2A10</field>
+ <field name="long_name">solute carrier family 2 (facilitated glucose transporter), member 10</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.1</field>
+ <field name="info">
+Arterial tortuosity syndrome [MIM:208050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC2A1">
+ <field name="name">SLC2A1</field>
+ <field name="long_name">solute carrier family 2 (facilitated glucose transporter), member 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p35-p31.3</field>
+ <field name="info">
+Glucose transport defect, blood-brain barrier [MIM:606777]
+Paroxysmal exertion-induced dyskinesia and hemolytic anemia [MIM:612126]
+Dystonia-18 [MIM:612126]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC2A2">
+ <field name="name">SLC2A2</field>
+ <field name="long_name">solute carrier family 2 (facilitated glucose transporter), member 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.1-q26.3</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent
+Fanconi-Bickel syndrome [MIM:227810]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC2A4">
+ <field name="name">SLC2A4</field>
+ <field name="long_name">solute carrier family 2 (facilitated glucose transporter), member 4</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC2A9">
+ <field name="name">SLC2A9</field>
+ <field name="long_name">solute carrier family 2 (facilitated glucose transporter), member 9</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16-p15.3</field>
+ <field name="info">
+Uric acid concentration, serum, QTL 2 [MIM:612076]
+Hypouricemia, renal, 2 [MIM:612076]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC30A2">
+ <field name="name">SLC30A2</field>
+ <field name="long_name">solute carrier family 30 (zinc transporter), member 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.11</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC30A8">
+ <field name="name">SLC30A8</field>
+ <field name="long_name">solute carrier family 30 (zinc transporter), member 8</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.11</field>
+ <field name="info">
+Diabetes mellitus, noninsulin-dependent, susceptibility to [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC33A1">
+ <field name="name">SLC33A1</field>
+ <field name="long_name">solute carrier family 33 (acetyl-CoA transporter), member 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q25.31</field>
+ <field name="info">
+Spastic paraplegia-42 [MIM:612539]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC34A1">
+ <field name="name">SLC34A1</field>
+ <field name="long_name">solute carrier family 34 (sodium phosphate), member 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q35</field>
+ <field name="info">
+Nephrolithiasis/osteoporosis, hypophosphatemic, 1 [MIM:612286]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC34A2">
+ <field name="name">SLC34A2</field>
+ <field name="long_name">solute carrier family 34 (sodium phosphate), member 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15.31-p15.2</field>
+ <field name="info">
+Pulmonary alveolar microlithiasis [MIM:265100]
+Testicular microlithiasis [MIM:610441]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC34A3">
+ <field name="name">SLC34A3</field>
+ <field name="long_name">solute carrier family 34 (sodium phosphate), member 3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+Hypophosphatemic rickets with hypercalciuria [MIM:241530]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC35A1">
+ <field name="name">SLC35A1</field>
+ <field name="long_name">solute carrier family 35 (CMP-sialic acid transporter), member A1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q15</field>
+ <field name="info">
+Congenital disorder of glycosylation, type IIf [MIM:603585]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC35C1">
+ <field name="name">SLC35C1</field>
+ <field name="long_name">solute carrier family 35, member C1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p11.2</field>
+ <field name="info">
+Congenital disorder of glycosylation, type IIc [MIM:266265]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC35D1">
+ <field name="name">SLC35D1</field>
+ <field name="long_name">solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32-p31</field>
+ <field name="info">
+Schneckenbecken dysplasia [MIM:269250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC37A4">
+ <field name="name">SLC37A4</field>
+ <field name="long_name">solute carrier family 37 (glucose-6-phosphate transporter), member 4</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Glycogen storage disease Ib [MIM:232220]
+Glycogen storage disease Ic [MIM:232240]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC39A13">
+ <field name="name">SLC39A13</field>
+ <field name="long_name">solute carrier family 39 (zinc transporter), member 13</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p11.2</field>
+ <field name="info">
+Spondylocheirodysplasia, Ehlers-Danlos syndrome-like [MIM:612350]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC39A4">
+ <field name="name">SLC39A4</field>
+ <field name="long_name">solute carrier family 39 (zinc transporter), member 4</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.3</field>
+ <field name="info">
+Acrodermatitis enteropathica [MIM:201100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC3A1">
+ <field name="name">SLC3A1</field>
+ <field name="long_name">solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p16.3</field>
+ <field name="info">
+Cystinuria [MIM:220100]
+Homozygous 2p16 deletion syndrome [MIM:606407]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC40A1">
+ <field name="name">SLC40A1</field>
+ <field name="long_name">solute carrier family 40 (iron-regulated transporter), member 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q32</field>
+ <field name="info">
+Hemochromatosis, type 4 [MIM:606069]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC45A2">
+ <field name="name">SLC45A2</field>
+ <field name="long_name">solute carrier family 45, member 2</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p13.3</field>
+ <field name="info">
+Oculocutaneous albinism, type IV [MIM:606574]
+Skin/hair/eye pigmentation 5, black/nonblack hair [MIM:227240]
+Skin/hair/eye pigmentation 5, dark/fair skin [MIM:227240]
+Skin/hair/eye pigmentation 5, dark/light eyes [MIM:227240]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC46A1">
+ <field name="name">SLC46A1</field>
+ <field name="long_name">solute carrier family 46 (folate transporter), member 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.1</field>
+ <field name="info">
+Folate malabsorption, hereditary [MIM:229050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC4A10">
+ <field name="name">SLC4A10</field>
+ <field name="long_name">solute carrier family 4, sodium bicarbonate transporter, member 10</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q23-q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC4A11">
+ <field name="name">SLC4A11</field>
+ <field name="long_name">solute carrier family 4, sodium borate transporter, member 11</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p13-p12</field>
+ <field name="info">
+Corneal endothelial dystrophy 2 [MIM:217700]
+Corneal endothelial dystrophy and perceptive deafness [MIM:217400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC4A1">
+ <field name="name">SLC4A1</field>
+ <field name="long_name">solute carrier family 4, anion exchanger, member 1 (erythrocyte membrane protein band 3, Diego blood group)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+Ovalocytosis
+Spherocytosis, type 4 [MIM:612653]
+Malaria, resistance to [MIM:611162]
+Renal tubular acidosis, distal, AD [MIM:179800]
+Renal tubular acidosis, distal, AR [MIM:611590]
+Blood group, Diego [MIM:110500]
+Blood group, Waldner [MIM:112010]
+Blood group, Wright [MIM:112050]
+Blood group, Froese [MIM:601551]
+Blood group, Swann [MIM:601550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC4A4">
+ <field name="name">SLC4A4</field>
+ <field name="long_name">solute carrier family 4, sodium bicarbonate cotransporter, member 4</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21</field>
+ <field name="info">
+Renal tubular acidosis, proximal, with ocular abnormalities [MIM:604278]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC5A1">
+ <field name="name">SLC5A1</field>
+ <field name="long_name">solute carrier family 5 (sodium/glucose cotransporter), member 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.1</field>
+ <field name="info">
+Glucose/galactose malabsorption [MIM:606824]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC5A2">
+ <field name="name">SLC5A2</field>
+ <field name="long_name">solute carrier family 5 (sodium/glucose cotransporter), member 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p11.2</field>
+ <field name="info">
+Renal glucosuria [MIM:233100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC5A5">
+ <field name="name">SLC5A5</field>
+ <field name="long_name">solute carrier family 5 (sodium iodide symporter), member 5</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2-p12</field>
+ <field name="info">
+Hypothyroidism, congenital [MIM:274400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC6A14">
+ <field name="name">SLC6A14</field>
+ <field name="long_name">solute carrier family 6 (amino acid transporter), member 14</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq23-q24</field>
+ <field name="info">
+Obesity, susceptibility to, BMIQ11 [MIM:300306]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC6A19">
+ <field name="name">SLC6A19</field>
+ <field name="long_name">solute carrier family 6 (neutral amino acid transporter), member 19</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.33</field>
+ <field name="info">
+Hartnup disorder [MIM:234500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC6A1">
+ <field name="name">SLC6A1</field>
+ <field name="long_name">solute carrier family 6 (neurotransmitter transporter, GABA), member 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25-p24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC6A2">
+ <field name="name">SLC6A2</field>
+ <field name="long_name">solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q12.2</field>
+ <field name="info">
+Orthostatic intolerance [MIM:604715]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC6A3">
+ <field name="name">SLC6A3</field>
+ <field name="long_name">solute carrier family 6 (neurotransmitter transporter, dopamine), member 3</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.3</field>
+ <field name="info">
+Attention-deficit hyperactivity disorder, susceptibility to [MIM:143465]
+Nicotine dependence, protection against [MIM:188890]
+Major affective disorder [MIM:125480]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC6A4">
+ <field name="name">SLC6A4</field>
+ <field name="long_name">solute carrier family 6 (neurotransmitter transporter, serotonin), member 4</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.1-q12</field>
+ <field name="info">
+Anxiety-related personality traits [MIM:607834]
+Obsessive-compulsive disorder 1 [MIM:164230]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC6A5">
+ <field name="name">SLC6A5</field>
+ <field name="long_name">solute carrier family 6 (neurotransmitter transporter, glycine), member 5</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.2-p15.1</field>
+ <field name="info">
+Hyperekplexia [MIM:149400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC6A8">
+ <field name="name">SLC6A8</field>
+ <field name="long_name">solute carrier family 6 (neurotransmitter transporter, creatine), member 8</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Creatine deficiency syndrome, X-linked [MIM:300352]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC7A1">
+ <field name="name">SLC7A1</field>
+ <field name="long_name">solute carrier family 7 (cationic amino acid transporter, y+ system), member 1</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC7A5">
+ <field name="name">SLC7A5</field>
+ <field name="long_name">solute carrier family 7 (cationic amino acid transporter, y+ system), member 5</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC7A7">
+ <field name="name">SLC7A7</field>
+ <field name="long_name">solute carrier family 7 (cationic amino acid transporter, y+ system), member 7</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2</field>
+ <field name="info">
+Lysinuric protein intolerance [MIM:222700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC7A9">
+ <field name="name">SLC7A9</field>
+ <field name="long_name">solute carrier family 7 (cationic amino acid transporter, y+ system), member 9</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+Cystinuria, type III
+Cystinuria, type II</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC9A3R1">
+ <field name="name">SLC9A3R1</field>
+ <field name="long_name">solute carrier family 9 (sodium/hydrogen exchanger), member 3 regulator 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25.1</field>
+ <field name="info">
+Nephrolithiasis/osteoporosis, hypophosphatemic, 2 [MIM:612287]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC9A6">
+ <field name="name">SLC9A6</field>
+ <field name="long_name">solute carrier family 9 (sodium/hydrogen exchanger), member 6</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26.3</field>
+ <field name="info">
+Mental retardation, X-linked syndromic, Christianson type [MIM:300243]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLC9A9">
+ <field name="name">SLC9A9</field>
+ <field name="long_name">solute carrier family 9 (sodium/hydrogen exchanger), member 9</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLCO1B1">
+ <field name="name">SLCO1B1</field>
+ <field name="long_name">solute carrier organic anion transporter family, member 1B1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEB12">
+ <field name="name">SLEB12</field>
+ <field name="long_name">Systemic lupus erythematosus, susceptibility to, 12</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23.1</field>
+ <field name="info">
+Systemic lupus erythematosus, susceptibility to, 12</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEB13">
+ <field name="name">SLEB13</field>
+ <field name="long_name">Systemic lupus erythematosus, susceptibility to, 13</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23</field>
+ <field name="info">
+Systemic lupus erythematosus, susceptibility to, 13</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEB1">
+ <field name="name">SLEB1</field>
+ <field name="long_name">systemic lupus erythematosus susceptibility 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q41-q42</field>
+ <field name="info">
+Systemic lupus erythematosus, susceptibility to, 1 [MIM:152700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEB2">
+ <field name="name">SLEB2</field>
+ <field name="long_name">systemic lupus erythematosus susceptibility 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.3</field>
+ <field name="info">
+Systemic lupus erythematosus, susceptibility to, 2, 605218 [MIM:152700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEB3">
+ <field name="name">SLEB3</field>
+ <field name="long_name">systemic lupus erythematosus susceptibility 3</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16-p15.2</field>
+ <field name="info">
+Systemic lupus erythematosus, susceptibility to, 3 [MIM:152700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEB4">
+ <field name="name">SLEB4</field>
+ <field name="long_name">systemic lupus erythematosus, susceptibility to, 4</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24</field>
+ <field name="info">
+Systemic lupus erythematosus, susceptibility to, 4 [MIM:152700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEB5">
+ <field name="name">SLEB5</field>
+ <field name="long_name">Systemic lupus erythematosus, susceptibility to, 5</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q32</field>
+ <field name="info">
+Systemic lupus erythematosus, susceptibility to, 5 [MIM:152700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEB7">
+ <field name="name">SLEB7</field>
+ <field name="long_name">Systemic lupus erythematosus, susceptibility to, 7</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p12</field>
+ <field name="info">
+Systemic lupus erythematosus, susceptibility to, 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEB8">
+ <field name="name">SLEB8</field>
+ <field name="long_name">Systemic lupus erythematosus, susceptibility to, 8</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13</field>
+ <field name="info">
+Systemic lupus erythematosus, susceptibility to, 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEH1">
+ <field name="name">SLEH1</field>
+ <field name="long_name">systemic lupus erythematosus with hemolytic anemia 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q14</field>
+ <field name="info">
+Systemic lupus erythematosus with hemolytic anemia [MIM:152700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEN1">
+ <field name="name">SLEN1</field>
+ <field name="long_name">systemic lupus erythematosus with nephritis 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.3</field>
+ <field name="info">
+Systemic lupus erythematosus with nephritis, susceptibility to, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEN2">
+ <field name="name">SLEN2</field>
+ <field name="long_name">systemic lupus erythematosus with nephritis 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q34-q35</field>
+ <field name="info">
+Systemic lupus erythematosus with nephritis, susceptibility to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEN3">
+ <field name="name">SLEN3</field>
+ <field name="long_name">systemic lupus erythematosus with nephritis 3</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Systemic lupus erythematosus with nephritis, susceptibility to, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLEV1">
+ <field name="name">SLEV1</field>
+ <field name="long_name">systemic lupus erythematosus, vitiligo-related 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13</field>
+ <field name="info">
+Vitiligo-associated multiple autoimmune disease susceptibility 1 [MIM:606579]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLI1">
+ <field name="name">SLI1</field>
+ <field name="long_name">Specific language impairment QTL, 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q</field>
+ <field name="info">
+Specific language impairment QTL, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLI2">
+ <field name="name">SLI2</field>
+ <field name="long_name">Specific language impairment QTL, 2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q</field>
+ <field name="info">
+Specific language impairment QTL, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLI3">
+ <field name="name">SLI3</field>
+ <field name="long_name">Specific language impairment QTL, 3</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q21</field>
+ <field name="info">
+Specific language impairment QTL, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLI4">
+ <field name="name">SLI4</field>
+ <field name="long_name">Specific language impairment 4</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q35-q36</field>
+ <field name="info">
+Specific language impairment 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLITRK1">
+ <field name="name">SLITRK1</field>
+ <field name="long_name">SLIT and NTRK-like family, member 1</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q31</field>
+ <field name="info">
+Tourette syndrome [MIM:137580]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLSN3">
+ <field name="name">SLSN3</field>
+ <field name="long_name">Senior-Loken syndrome 3</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q22</field>
+ <field name="info">
+Senior-Loken syndrome 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SLURP1">
+ <field name="name">SLURP1</field>
+ <field name="long_name">secreted LY6/PLAUR domain containing 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8qter</field>
+ <field name="info">
+Meleda disease [MIM:248300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SM1">
+ <field name="name">SM1</field>
+ <field name="long_name">Schistosoma mansoni, susceptibility/resistance to</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31-q33</field>
+ <field name="info">
+Schistosoma mansoni infection, susceptibility/resistance to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SM2">
+ <field name="name">SM2</field>
+ <field name="long_name">Hepatic fibrosis susceptibility due to Schistosoma mansoni infection</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q22-q23</field>
+ <field name="info">
+Hepatic fibrosis susceptibility due to Schistosoma mansoni infection</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMA4">
+ <field name="name">SMA4</field>
+ <field name="long_name">glucuronidase, beta pseudogene</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q12.2-q13.3</field>
+ <field name="info">
+Spinal muscular atrophy-1 [MIM:253300]
+Spinal muscular atrophy-2 [MIM:253550]
+Spinal muscular atrophy-3 [MIM:253400]
+Spinal muscular atrophy-4 [MIM:271150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMAD1">
+ <field name="name">SMAD1</field>
+ <field name="long_name">SMAD family member 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, type 2D [MIM:601472]
+Neuropathy, distal hereditary motor, type V [MIM:600794]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMAD2">
+ <field name="name">SMAD2</field>
+ <field name="long_name">SMAD family member 2</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMAD3">
+ <field name="name">SMAD3</field>
+ <field name="long_name">SMAD family member 3</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21-q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMAD4">
+ <field name="name">SMAD4</field>
+ <field name="long_name">SMAD family member 4</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.1</field>
+ <field name="info">
+Pancreatic cancer
+Polyposis, juvenile intestinal [MIM:174900]
+Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome [MIM:175050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMAD7">
+ <field name="name">SMAD7</field>
+ <field name="long_name">SMAD family member 7</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.1</field>
+ <field name="info">
+Colorectal cancer, susceptiblity to, 3 [MIM:612229]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMAL">
+ <field name="name">SMAL</field>
+ <field name="long_name">spinal muscular atrophy, congenital nonprogressive, of lower limbs</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q23-q24</field>
+ <field name="info">
+Spinal muscular atrophy, congenital nonprogressive, of lower limbs</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMARCAL1">
+ <field name="name">SMARCAL1</field>
+ <field name="long_name">SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q34-q36</field>
+ <field name="info">
+Schimke immunoosseous dysplasia [MIM:242900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMARCB1">
+ <field name="name">SMARCB1</field>
+ <field name="long_name">SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11</field>
+ <field name="info">
+Rhabdoid tumors
+Rhabdoid predisposition syndrome, familial</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMAR">
+ <field name="name">SMAR</field>
+ <field name="long_name">Spinal muscular atrophy, chronic distal, autosomal recessive</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Spinal muscular atrophy, chronic distal, autosomal recessive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMAX3">
+ <field name="name">SMAX3</field>
+ <field name="long_name">spinal muscular atrophy, distal, X-linked recessive</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.1-q21</field>
+ <field name="info">
+Spinal muscular atrophy, distal, X-linked 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMC3">
+ <field name="name">SMC3</field>
+ <field name="long_name">structural maintenance of chromosomes 3</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q25</field>
+ <field name="info">
+Cornelia de Lange syndrome 3 [MIM:610759]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMCR">
+ <field name="name">SMCR</field>
+ <field name="long_name">Smith-Magenis syndrome chromosome region</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+Smith-Magenis syndrome [MIM:182290]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMG1">
+ <field name="name">SMG1</field>
+ <field name="long_name">SMG1 homolog, phosphatidylinositol 3-kinase-related kinase (C. elegans)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMN1">
+ <field name="name">SMN1</field>
+ <field name="long_name">survival of motor neuron 1, telomeric</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q12.2-q13.3</field>
+ <field name="info">
+Spinal muscular atrophy-1 [MIM:253300]
+Spinal muscular atrophy-2 [MIM:253550]
+Spinal muscular atrophy-3 [MIM:253400]
+Spinal muscular atrophy-4 [MIM:271150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMN2">
+ <field name="name">SMN2</field>
+ <field name="long_name">survival of motor neuron 2, centromeric</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q12.2-q13.3</field>
+ <field name="info">
+Spinal Muscular Atrophy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMO">
+ <field name="name">SMO</field>
+ <field name="long_name">smoothened homolog (Drosophila)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31-q32</field>
+ <field name="info">
+Basal cell carcinoma, somatic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMPD1">
+ <field name="name">SMPD1</field>
+ <field name="long_name">sphingomyelin phosphodiesterase 1, acid lysosomal</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.4-p15.1</field>
+ <field name="info">
+Niemann-Pick disease, type A [MIM:257200]
+Niemann-Pick disease, type B [MIM:607616]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMS">
+ <field name="name">SMS</field>
+ <field name="long_name">spermine synthase</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.1</field>
+ <field name="info">
+Mental retardation, X-linked, Snyder-Robinson type [MIM:309583]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SMUG1">
+ <field name="name">SMUG1</field>
+ <field name="long_name">single-strand-selective monofunctional uracil-DNA glycosylase 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SNAI2">
+ <field name="name">SNAI2</field>
+ <field name="long_name">snail homolog 2 (Drosophila)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q11</field>
+ <field name="info">
+Waardenburg syndrome, type IID [MIM:608890]
+Melanoma metastasis, modification of
+Piebaldism [MIM:172800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SNAP29">
+ <field name="name">SNAP29</field>
+ <field name="long_name">synaptosomal-associated protein, 29kDa</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MIM:609528]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SNAX1">
+ <field name="name">SNAX1</field>
+ <field name="long_name">sensory ataxia 1 (autosomal dominant)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p12-q12.1</field>
+ <field name="info">
+Ataxia, sensory, autosomal dominant</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SNCAIP">
+ <field name="name">SNCAIP</field>
+ <field name="long_name">synuclein, alpha interacting protein</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q23.1-q23.3</field>
+ <field name="info">
+Parkinson disease [MIM:168600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SNCA">
+ <field name="name">SNCA</field>
+ <field name="long_name">synuclein, alpha (non A4 component of amyloid precursor)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21</field>
+ <field name="info">
+Parkinson disease, familial [MIM:168601]
+Parkinson disease 4, autosomal dominant Lewy body [MIM:605543]
+Dementia, Lewy body [MIM:127750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SNCB">
+ <field name="name">SNCB</field>
+ <field name="long_name">synuclein, beta</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q35</field>
+ <field name="info">
+Dementia, Lewy body [MIM:127750]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SNRPN">
+ <field name="name">SNRPN</field>
+ <field name="long_name">small nuclear ribonucleoprotein polypeptide N</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q12</field>
+ <field name="info">
+Prader-Willi syndrome [MIM:176270]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SNX3">
+ <field name="name">SNX3</field>
+ <field name="long_name">sorting nexin 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q21</field>
+ <field name="info">
+Microphthalmia, syndromic 8 [MIM:601349]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SOCS1">
+ <field name="name">SOCS1</field>
+ <field name="long_name">suppressor of cytokine signaling 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SOCS3">
+ <field name="name">SOCS3</field>
+ <field name="long_name">suppressor of cytokine signaling 3</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25.3</field>
+ <field name="info">
+Dermatitis, atopic, 4 [MIM:605805]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SOD1">
+ <field name="name">SOD1</field>
+ <field name="long_name">superoxide dismutase 1, soluble</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.1</field>
+ <field name="info">
+Amyotrophic lateral sclerosis, due to SOD1 deficiency [MIM:105400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SOD2">
+ <field name="name">SOD2</field>
+ <field name="long_name">superoxide dismutase 2, mitochondrial</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SOD3">
+ <field name="name">SOD3</field>
+ <field name="long_name">superoxide dismutase 3, extracellular</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15.3-p15.1</field>
+ <field name="info">
+Superoxide dismutase, elevated extracellular</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SORBS1">
+ <field name="name">SORBS1</field>
+ <field name="long_name">sorbin and SH3 domain containing 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23.3-q24.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SORD">
+ <field name="name">SORD</field>
+ <field name="long_name">sorbitol dehydrogenase</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15.3</field>
+ <field name="info">
+Cataract, congenital</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SORL1">
+ <field name="name">SORL1</field>
+ <field name="long_name">sortilin-related receptor, L(DLR class) A repeats-containing</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.2-q24.2</field>
+ <field name="info">
+Alzheimer disease, pathogenesis, association with [MIM:104300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SOS1">
+ <field name="name">SOS1</field>
+ <field name="long_name">son of sevenless homolog 1 (Drosophila)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p22-p21</field>
+ <field name="info">
+Fibromatosis, gingival [MIM:135300]
+Noonan syndrome 4 [MIM:610733]
+Noonan-like/multiple giant cell lesion syndrome [MIM:163955]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SOST">
+ <field name="name">SOST</field>
+ <field name="long_name">sclerosteosis</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12-q21</field>
+ <field name="info">
+Sclerosteosis [MIM:269500]
+Van Buchem disease [MIM:239100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SOX10">
+ <field name="name">SOX10</field>
+ <field name="long_name">SRY (sex determining region Y)-box 10</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13</field>
+ <field name="info">
+Waardenburg-Shah syndrome [MIM:277580]
+Yemenite deaf-blind hypopigmentation syndrome [MIM:601706]
+PCWH [MIM:609136]
+Waardenburg syndrome, type IIE [MIM:611584]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SOX18">
+ <field name="name">SOX18</field>
+ <field name="long_name">SRY (sex determining region Y)-box 18</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.33</field>
+ <field name="info">
+Hypotrichosis-lymphedema-telangiectasia syndrome [MIM:607823]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SOX2">
+ <field name="name">SOX2</field>
+ <field name="long_name">SRY (sex determining region Y)-box 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.3-q27</field>
+ <field name="info">
+Microphthalmia, syndromic 3 [MIM:206900]
+Optic nerve hypoplasia and abnormalities of the central nervous system [MIM:206900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SOX3">
+ <field name="name">SOX3</field>
+ <field name="long_name">SRY (sex determining region Y)-box 3</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26.3</field>
+ <field name="info">
+Mental retardation, X-linked, with isolated growth hormone deficiency [MIM:300123]
+Panhypopituitarism, X-linked [MIM:312000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SOX8">
+ <field name="name">SOX8</field>
+ <field name="long_name">SRY (sex determining region Y)-box 8</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SOX9">
+ <field name="name">SOX9</field>
+ <field name="long_name">SRY (sex determining region Y)-box 9</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q24.3-q25.1</field>
+ <field name="info">
+Campomelic dysplasia with autosomal sex reversal [MIM:114290]
+Acampomelic campomelic dysplasia [MIM:114290]
+Campomelic dysplasia [MIM:114290]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SP110">
+ <field name="name">SP110</field>
+ <field name="long_name">SP110 nuclear body protein</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37.1</field>
+ <field name="info">
+Hepatic venoocclusive disease with immunodeficiency [MIM:235550]
+Mycobacterium tuberculosis, susceptibility to [MIM:607948]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPAG16">
+ <field name="name">SPAG16</field>
+ <field name="long_name">sperm associated antigen 16</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q34</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPAST">
+ <field name="name">SPAST</field>
+ <field name="long_name">spastin</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p22-p21</field>
+ <field name="info">
+Spastic paraplegia-4 [MIM:182601]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPATA16">
+ <field name="name">SPATA16</field>
+ <field name="long_name">spermatogenesis associated 16</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.3</field>
+ <field name="info">
+Globozoospermia [MIM:102530]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPATA7">
+ <field name="name">SPATA7</field>
+ <field name="long_name">spermatogenesis associated 7</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q31.3</field>
+ <field name="info">
+Leber congenital amaurosis 3 [MIM:604232]
+Retinitis pigmentosa, juvenile, autosomal recessive [MIM:268000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPD3">
+ <field name="name">SPD3</field>
+ <field name="long_name">Synpolydactyly 3</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2-q12</field>
+ <field name="info">
+Synpolydactyly 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPDA2">
+ <field name="name">SPDA2</field>
+ <field name="long_name">Spondyloarthropathy, susceptiblity to, 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q31-q34</field>
+ <field name="info">
+Spondyloarthropathy, susceptiblity to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPEN">
+ <field name="name">SPEN</field>
+ <field name="long_name">spen homolog, transcriptional regulator (Drosophila)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13</field>
+ <field name="info">
+Megakaryoblastic leukemia, acute</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG11">
+ <field name="name">SPG11</field>
+ <field name="long_name">spastic paraplegia 11 (autosomal recessive)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21.1</field>
+ <field name="info">
+Spastic paraplegia-11 [MIM:604360]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG12">
+ <field name="name">SPG12</field>
+ <field name="long_name">spastic paraplegia 12 (autosomal dominant)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13</field>
+ <field name="info">
+Spastic paraplegia-12</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG14">
+ <field name="name">SPG14</field>
+ <field name="long_name">spastic paraplegia 14 (autosomal recessive)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27-q28</field>
+ <field name="info">
+Spastic paraplegia 14, autosomal recessive</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG16">
+ <field name="name">SPG16</field>
+ <field name="long_name">spastic paraplegia 16 (complicated, X-linked recessive)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq11.2</field>
+ <field name="info">
+Spastic paraplegia-16, X-linked, complicated</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG19">
+ <field name="name">SPG19</field>
+ <field name="long_name">spastic paraplegia 19 (autosomal dominant)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q</field>
+ <field name="info">
+Spastic paraplegia-19</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG20">
+ <field name="name">SPG20</field>
+ <field name="long_name">spastic paraplegia 20 (Troyer syndrome)</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12.3</field>
+ <field name="info">
+Troyer syndrome [MIM:275900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG21">
+ <field name="name">SPG21</field>
+ <field name="long_name">spastic paraplegia 21 (autosomal recessive, Mast syndrome)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21-q22</field>
+ <field name="info">
+Mast syndrome [MIM:248900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG24">
+ <field name="name">SPG24</field>
+ <field name="long_name">spastic paraplegia 24 (autosomal recessive)</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14</field>
+ <field name="info">
+Spastic paraplegia 24</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG25">
+ <field name="name">SPG25</field>
+ <field name="long_name">spastic paraplegia 25 (autosomal recessive, with disc herniation)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23-q24.1</field>
+ <field name="info">
+Spastic paraplegia 25</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG26">
+ <field name="name">SPG26</field>
+ <field name="long_name">spastic paraplegia 26</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p11.1-q14</field>
+ <field name="info">
+Spastic paraplegia 26</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG27">
+ <field name="name">SPG27</field>
+ <field name="long_name">spastic paraplegia 27 (autosomal recessive)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.1-q24.1</field>
+ <field name="info">
+Spastic paraplegia-27</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG28">
+ <field name="name">SPG28</field>
+ <field name="long_name">spastic paraplegia 28 (autosomal recessive)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q21.3-q22.3</field>
+ <field name="info">
+Spastic paraplegia-28</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG29">
+ <field name="name">SPG29</field>
+ <field name="long_name">spastic paraplegia 29 (autosomal dominant)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p31.1-p21.1</field>
+ <field name="info">
+Spastic paraplegia-29</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG34">
+ <field name="name">SPG34</field>
+ <field name="long_name">spastic paraplegia 34 (autosomal dominant)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24-q25</field>
+ <field name="info">
+Spastic paraplegia 34, X-linked</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG35">
+ <field name="name">SPG35</field>
+ <field name="long_name">spastic paraplegia 35 (autosomal recessive)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q21-q23.1</field>
+ <field name="info">
+Spastic paraplegia-35</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG37">
+ <field name="name">SPG37</field>
+ <field name="long_name">spastic paraplegia 37 (autosomal dominant)</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p21.1-q13.3</field>
+ <field name="info">
+Spastic paraplegia-37</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG7">
+ <field name="name">SPG7</field>
+ <field name="long_name">spastic paraplegia 7 (pure and complicated autosomal recessive)</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24.3</field>
+ <field name="info">
+Spastic paraplegia-7 [MIM:607259]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPG9">
+ <field name="name">SPG9</field>
+ <field name="long_name">spastic paraplegia 9 (autosomal dominant)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23.3-q24.1</field>
+ <field name="info">
+Spastic paraplegia-9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPINK1">
+ <field name="name">SPINK1</field>
+ <field name="long_name">serine peptidase inhibitor, Kazal type 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q32</field>
+ <field name="info">
+Pancreatitis, hereditary [MIM:167800]
+Fibrocalculous pancreatic diabetes, susceptibility to
+Tropical calcific pancreatitis [MIM:608189]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPINK5">
+ <field name="name">SPINK5</field>
+ <field name="long_name">serine peptidase inhibitor, Kazal type 5</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q32</field>
+ <field name="info">
+Netherton syndrome [MIM:256500]
+Atopy [MIM:147050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPINT2">
+ <field name="name">SPINT2</field>
+ <field name="long_name">serine peptidase inhibitor, Kunitz type, 2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+Diarrhea 3, secretory sodium, congenital, syndromic [MIM:270420]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPOAN">
+ <field name="name">SPOAN</field>
+ <field name="long_name">spastic paraplegia, optic atrophy, and neuropathy</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Spastic paraplegia, optic atrophy, and neuropathy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPP1">
+ <field name="name">SPP1</field>
+ <field name="long_name">secreted phosphoprotein 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q21-q25</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPRED1">
+ <field name="name">SPRED1</field>
+ <field name="long_name">sprouty-related, EVH1 domain containing 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q13.2</field>
+ <field name="info">
+Neurofibromatosis, type 1-like syndrome [MIM:611431]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPRN">
+ <field name="name">SPRN</field>
+ <field name="long_name">shadow of prion protein homolog (zebrafish)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q26.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPRY2">
+ <field name="name">SPRY2</field>
+ <field name="long_name">sprouty homolog 2 (Drosophila)</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q31.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPR">
+ <field name="name">SPR</field>
+ <field name="long_name">sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p14-p12</field>
+ <field name="info">
+Dystonia, dopa-responsive, due to sepiapterin reductase deficiency [MIM:612716]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPSMA">
+ <field name="name">SPSMA</field>
+ <field name="long_name">scapuloperoneal spinal muscular atrophy, New England type (2)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.1-q24.31</field>
+ <field name="info">
+Scapuloperoneal spinal muscular atrophy, New England type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPTA1">
+ <field name="name">SPTA1</field>
+ <field name="long_name">spectrin, alpha, erythrocytic 1 (elliptocytosis 2)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21</field>
+ <field name="info">
+Elliptocytosis-2 [MIM:130600]
+Pyropoikilocytosis [MIM:266140]
+Spherocytosis, type 3 [MIM:270970]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPTBN2">
+ <field name="name">SPTBN2</field>
+ <field name="long_name">spectrin, beta, non-erythrocytic 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Spinocerebellar ataxia-5 [MIM:600224]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPTBN5">
+ <field name="name">SPTBN5</field>
+ <field name="long_name">spectrin, beta, non-erythrocytic 5</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPTB">
+ <field name="name">SPTB</field>
+ <field name="long_name">spectrin, beta, erythrocytic</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q22-q23.2</field>
+ <field name="info">
+Elliptocytosis-3
+Spherocytosis, type 2
+Anemia, neonatal hemolytic, fatal and near-fatal</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SPTLC1">
+ <field name="name">SPTLC1</field>
+ <field name="long_name">serine palmitoyltransferase, long chain base subunit 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22.1-q22.3</field>
+ <field name="info">
+Neuropathy, hereditary sensory and autonomic, type 1 [MIM:162400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SQSTM1">
+ <field name="name">SQSTM1</field>
+ <field name="long_name">sequestosome 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q35</field>
+ <field name="info">
+Paget disease of bone [MIM:602080]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SQTL1">
+ <field name="name">SQTL1</field>
+ <field name="long_name">Smoking as a quantitative trait locus 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22</field>
+ <field name="info">
+Smoking as a quantitative trait locus 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SQTL2">
+ <field name="name">SQTL2</field>
+ <field name="long_name">Smoking as a quantitative trait locus 2</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12</field>
+ <field name="info">
+Smoking as a quantitative trait locus 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SRC">
+ <field name="name">SRC</field>
+ <field name="long_name">v-src sarcoma (Schmidt-Ruppin A-2) viral oncogene homolog (avian)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q12-q13</field>
+ <field name="info">
+Colon cancer, advanced</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SRD5A2">
+ <field name="name">SRD5A2</field>
+ <field name="long_name">steroid-5-alpha-reductase, alpha polypeptide 2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 2)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p23</field>
+ <field name="info">
+Pseudovaginal perineoscrotal hypospadias [MIM:264600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SREBF1">
+ <field name="name">SREBF1</field>
+ <field name="long_name">sterol regulatory element binding transcription factor 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SREBF2">
+ <field name="name">SREBF2</field>
+ <field name="long_name">sterol regulatory element binding transcription factor 2</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SRI">
+ <field name="name">SRI</field>
+ <field name="long_name">sorcin</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SRPX2">
+ <field name="name">SRPX2</field>
+ <field name="long_name">sushi-repeat-containing protein, X-linked 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq21.33-q23</field>
+ <field name="info">
+Rolandic epilepsy, mental retardation, and speech dyspraxia [MIM:300643]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SRPX">
+ <field name="name">SRPX</field>
+ <field name="long_name">sushi-repeat-containing protein, X-linked</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SRR">
+ <field name="name">SRR</field>
+ <field name="long_name">serine racemase</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SRS">
+ <field name="name">SRS</field>
+ <field name="long_name">Snyder-Robinson X-linked mental retardation syndrome</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p11.2</field>
+ <field name="info">
+Silver-Russell syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SRY">
+ <field name="name">SRY</field>
+ <field name="long_name">sex determining region Y</field>
+ <field name="chromosome">Y</field>
+ <field name="location">Yp11.3</field>
+ <field name="info">
+Gonadal dysgenesis, XY female type [MIM:306100]
+Hermaphroditism, true [MIM:235600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SS18">
+ <field name="name">SS18</field>
+ <field name="long_name">synovial sarcoma translocation, chromosome 18</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q11.2</field>
+ <field name="info">
+Sarcoma, synovial</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SS3">
+ <field name="name">SS3</field>
+ <field name="long_name">Sarcoidosis, susceptibility to, 3</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.3</field>
+ <field name="info">
+Sarcoidosis, susceptibility to, 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SSD">
+ <field name="name">SSD</field>
+ <field name="long_name">Speech-sound disorder</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p12-q13</field>
+ <field name="info">
+Speech-sound disorder</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SSH1">
+ <field name="name">SSH1</field>
+ <field name="long_name">slingshot homolog 1 (Drosophila)</field>
+ <field name="chromosome">12</field>
+ <field name="location">12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SSTR2">
+ <field name="name">SSTR2</field>
+ <field name="long_name">somatostatin receptor 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SSTR5">
+ <field name="name">SSTR5</field>
+ <field name="long_name">somatostatin receptor 5</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+Somatostatin analog, resistance to [MIM:102200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SST">
+ <field name="name">SST</field>
+ <field name="long_name">somatostatin</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q28</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SSX1">
+ <field name="name">SSX1</field>
+ <field name="long_name">synovial sarcoma, X breakpoint 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.2</field>
+ <field name="info">
+Sarcoma, synovial</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SSX2">
+ <field name="name">SSX2</field>
+ <field name="long_name">synovial sarcoma, X breakpoint 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.2</field>
+ <field name="info">
+Sarcoma, synovial</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SSX4">
+ <field name="name">SSX4</field>
+ <field name="long_name">synovial sarcoma, X breakpoint 4</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.2</field>
+ <field name="info">
+Sarcoma, synovial</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ST11">
+ <field name="name">ST11</field>
+ <field name="long_name">suppression of tumorigenicity 11 (pancreas)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25</field>
+ <field name="info">
+Pancreatic endocrine tumors</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ST14">
+ <field name="name">ST14</field>
+ <field name="long_name">suppression of tumorigenicity 14 (colon carcinoma)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q24-q25</field>
+ <field name="info">
+Ichthyosis with hypotrichosis [MIM:610765]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ST2">
+ <field name="name">ST2</field>
+ <field name="long_name">suppression of tumorigenicity 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p14.3-p12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ST3">
+ <field name="name">ST3</field>
+ <field name="long_name">suppression of tumorigenicity 3</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Cervical carcinoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ST8">
+ <field name="name">ST8</field>
+ <field name="long_name">suppression of tumorigenicity 8 (ovarian)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q26-q27</field>
+ <field name="info">
+Ovarian cancer, serous</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STAR">
+ <field name="name">STAR</field>
+ <field name="long_name">steroidogenic acute regulatory protein</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p11.2</field>
+ <field name="info">
+Lipoid adrenal hyperplasia [MIM:201710]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STAT1">
+ <field name="name">STAT1</field>
+ <field name="long_name">signal transducer and activator of transcription 1, 91kDa</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q32.2-q32.3</field>
+ <field name="info">
+Mycobacterial infection, atypical, familial disseminated [MIM:209950]
+STAT1 deficiency, complete</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STAT3">
+ <field name="name">STAT3</field>
+ <field name="long_name">signal transducer and activator of transcription 3 (acute-phase response factor)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+Hyperimmunoglobulin E recurrent infection syndrome [MIM:147060]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STAT4">
+ <field name="name">STAT4</field>
+ <field name="long_name">signal transducer and activator of transcription 4</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q32.2-q32.3</field>
+ <field name="info">
+Rheumatoid arthritis, association with [MIM:180300]
+Systemic lupus erythematous, association with susceptibility to, 11 [MIM:612253]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STAT5B">
+ <field name="name">STAT5B</field>
+ <field name="long_name">signal transducer and activator of transcription 5B</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2</field>
+ <field name="info">
+Leukemia, acute promyelocytic, STAT5B/RARA type
+Growth hormone insensitivity with immunodeficiency [MIM:245590]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STAT6">
+ <field name="name">STAT6</field>
+ <field name="long_name">signal transducer and activator of transcription 6, interleukin-4 induced</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="STBMS1">
+ <field name="name">STBMS1</field>
+ <field name="long_name">Strabismus, susceptibility to, 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p22.1</field>
+ <field name="info">
+Strabismus, susceptibility to, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STHAG5">
+ <field name="name">STHAG5</field>
+ <field name="long_name">tooth agenesis, selective, 5</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q11.2-q21</field>
+ <field name="info">
+Tooth agenesis, selective, 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STH">
+ <field name="name">STH</field>
+ <field name="long_name">saitohin</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="STIL">
+ <field name="name">STIL</field>
+ <field name="long_name">SCL/TAL1 interrupting locus</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+Microcephaly, primary autosomal recessive, 7 [MIM:612703]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STIM1">
+ <field name="name">STIM1</field>
+ <field name="long_name">stromal interaction molecule 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Immune dysfunction, with T-cell inactivation due to calcium entry defect 2 [MIM:612783]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STK11">
+ <field name="name">STK11</field>
+ <field name="long_name">serine/threonine kinase 11</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Peutz-Jeghers syndrome [MIM:175200]
+Melanoma, malignant sporadic
+Pancreatic cancer, sporadic
+Testicular tumor, sporadic [MIM:273300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STK19">
+ <field name="name">STK19</field>
+ <field name="long_name">serine/threonine kinase 19</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="STK33">
+ <field name="name">STK33</field>
+ <field name="long_name">serine/threonine kinase 33</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="STOX1">
+ <field name="name">STOX1</field>
+ <field name="long_name">storkhead box 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.1</field>
+ <field name="info">
+Preeclampsia/eclampsia 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL10">
+ <field name="name">STQTL10</field>
+ <field name="long_name">Stature QTL 10</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q23</field>
+ <field name="info">
+Stature QTL 10</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL11">
+ <field name="name">STQTL11</field>
+ <field name="long_name">Stature QTL 11</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21</field>
+ <field name="info">
+Stature QTL 11</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL12">
+ <field name="name">STQTL12</field>
+ <field name="long_name">Stature QTL 12</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q31</field>
+ <field name="info">
+Stature QTL 12</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL13">
+ <field name="name">STQTL13</field>
+ <field name="long_name">Stature QTL 13</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15.3</field>
+ <field name="info">
+Stature QTL 13</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL14">
+ <field name="name">STQTL14</field>
+ <field name="long_name">Stature QTL 14</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11.22</field>
+ <field name="info">
+Stature QTL 14</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL15">
+ <field name="name">STQTL15</field>
+ <field name="long_name">Stature QTL 15</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21.13</field>
+ <field name="info">
+Stature QTL 15</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL16">
+ <field name="name">STQTL16</field>
+ <field name="long_name">Stature QTL 16</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22.32</field>
+ <field name="info">
+Stature QTL 16</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL17">
+ <field name="name">STQTL17</field>
+ <field name="long_name">Stature QTL 17</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15</field>
+ <field name="info">
+Stature QTL 17</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL2">
+ <field name="name">STQTL2</field>
+ <field name="long_name">stature quantitative trait locus 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31.3</field>
+ <field name="info">
+Stature QTL 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL3">
+ <field name="name">STQTL3</field>
+ <field name="long_name">stature quantitative trait locus 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p11.2-q14</field>
+ <field name="info">
+Stature QTL 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL4">
+ <field name="name">STQTL4</field>
+ <field name="long_name">stature quantitative trait locus 4</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q32-q33</field>
+ <field name="info">
+Stature QTL 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL5">
+ <field name="name">STQTL5</field>
+ <field name="long_name">stature quantitative trait locus 5</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26</field>
+ <field name="info">
+Stature QTL 5</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL6">
+ <field name="name">STQTL6</field>
+ <field name="long_name">stature quantitative trait locus 6</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24-q25</field>
+ <field name="info">
+Stature QTL 6</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL7">
+ <field name="name">STQTL7</field>
+ <field name="long_name">stature quantitative trait locus 7</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p21</field>
+ <field name="info">
+Stature QTL 7</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STQTL8">
+ <field name="name">STQTL8</field>
+ <field name="long_name">stature quantitative trait locus 8</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22</field>
+ <field name="info">
+Stature QTL 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STRA6">
+ <field name="name">STRA6</field>
+ <field name="long_name">stimulated by retinoic acid gene 6 homolog (mouse)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q24.1</field>
+ <field name="info">
+Microphthalmia, syndromic 9 [MIM:601186]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STRADA">
+ <field name="name">STRADA</field>
+ <field name="long_name">STE20-related kinase adaptor alpha</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q23.3</field>
+ <field name="info">
+Polyhydramnios, megalencephaly, and symptomatic epilepsy [MIM:611087]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STRC">
+ <field name="name">STRC</field>
+ <field name="long_name">stereocilin</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15</field>
+ <field name="info">
+Deafness, autosomal recessive 16 [MIM:603720]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STS">
+ <field name="name">STS</field>
+ <field name="long_name">steroid sulfatase (microsomal), isozyme S</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.32</field>
+ <field name="info">
+Ichthyosis, X-linked [MIM:308100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STUT1">
+ <field name="name">STUT1</field>
+ <field name="long_name">Stuttering, familial persistent 1</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.3-p11.2</field>
+ <field name="info">
+Stuttering, familial persistent 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STUT2">
+ <field name="name">STUT2</field>
+ <field name="long_name">Stuttering, familial persistent 2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.1</field>
+ <field name="info">
+Stuttering, familial persistent 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STX11">
+ <field name="name">STX11</field>
+ <field name="long_name">syntaxin 11</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q24</field>
+ <field name="info">
+Hemophagocytic lymphohistiocytosis, familial, 4 [MIM:603552]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STX16">
+ <field name="name">STX16</field>
+ <field name="long_name">syntaxin 16</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.32</field>
+ <field name="info">
+Pseudohypoparathyroidism, type IB [MIM:603233]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="STX1A">
+ <field name="name">STX1A</field>
+ <field name="long_name">syntaxin 1A (brain)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="STXBP1">
+ <field name="name">STXBP1</field>
+ <field name="long_name">syntaxin binding protein 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34.1</field>
+ <field name="info">
+Epileptic encephalopathy, early infantile, 4 [MIM:612164]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SUCLA2">
+ <field name="name">SUCLA2</field>
+ <field name="long_name">succinate-CoA ligase, ADP-forming, beta subunit</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q12.2-q13</field>
+ <field name="info">
+Mitochondrial DNA depletion syndrome, enceophalomyopathic form, with methylmalonic aciduria [MIM:612073]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SUCLG1">
+ <field name="name">SUCLG1</field>
+ <field name="long_name">succinate-CoA ligase, alpha subunit</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p11.2</field>
+ <field name="info">
+Lactic acidosis, fatal infantile [MIM:245400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SUFU">
+ <field name="name">SUFU</field>
+ <field name="long_name">suppressor of fused homolog (Drosophila)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24-q25</field>
+ <field name="info">
+Medulloblastoma, desmoplastic [MIM:155255]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SULT1A1">
+ <field name="name">SULT1A1</field>
+ <field name="long_name">sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12.1-p11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SULT1A3">
+ <field name="name">SULT1A3</field>
+ <field name="long_name">sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SULT1C2">
+ <field name="name">SULT1C2</field>
+ <field name="long_name">sulfotransferase family, cytosolic, 1C, member 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SULT2B1">
+ <field name="name">SULT2B1</field>
+ <field name="long_name">sulfotransferase family, cytosolic, 2B, member 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SUMF1">
+ <field name="name">SUMF1</field>
+ <field name="long_name">sulfatase modifying factor 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26</field>
+ <field name="info">
+Multiple sulfatase deficiency [MIM:272200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SUMO1">
+ <field name="name">SUMO1</field>
+ <field name="long_name">SMT3 suppressor of mif two 3 homolog 1 (S. cerevisiae)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q32.2-q33</field>
+ <field name="info">
+Orofacial cleft 10</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SUMO4">
+ <field name="name">SUMO4</field>
+ <field name="long_name">SMT3 suppressor of mif two 3 homolog 4 (S. cerevisiae)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25</field>
+ <field name="info">
+Diabetes mellitus, insulin-dependent, 5 [MIM:600320]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SUOX">
+ <field name="name">SUOX</field>
+ <field name="long_name">sulfite oxidase</field>
+ <field name="chromosome">12</field>
+ <field name="location">12</field>
+ <field name="info">
+Sulfite oxidase deficiency [MIM:272300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SURF1">
+ <field name="name">SURF1</field>
+ <field name="long_name">surfeit 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+Leigh syndrome, due to COX deficiency [MIM:256000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SXI2">
+ <field name="name">SXI2</field>
+ <field name="long_name">X inactivation, familial skewed, 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq25-q26</field>
+ <field name="info">
+X inactivation, familial skewed, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SYCP3">
+ <field name="name">SYCP3</field>
+ <field name="long_name">synaptonemal complex protein 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q23</field>
+ <field name="info">
+Azoospermia due to perturbations of meiosis [MIM:270960]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SYN1">
+ <field name="name">SYN1</field>
+ <field name="long_name">synapsin I</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.4-p11.2</field>
+ <field name="info">
+Epilepsy, X-linked, with variable learning disabilities and behavior disorders [MIM:300491]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SYN2">
+ <field name="name">SYN2</field>
+ <field name="long_name">synapsin II</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25</field>
+ <field name="info">
+Schizophrenia, susceptibility to [MIM:181500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SYN3">
+ <field name="name">SYN3</field>
+ <field name="long_name">synapsin III</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SYNE1">
+ <field name="name">SYNE1</field>
+ <field name="long_name">spectrin repeat containing, nuclear envelope 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25</field>
+ <field name="info">
+Spinocerebellar ataxia, autosomal recessive 8 [MIM:610743]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SYNE2">
+ <field name="name">SYNE2</field>
+ <field name="long_name">spectrin repeat containing, nuclear envelope 2</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SYNGR1">
+ <field name="name">SYNGR1</field>
+ <field name="long_name">synaptogyrin 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="SYNSTH">
+ <field name="name">SYNSTH</field>
+ <field name="long_name">Synesthesia</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q24.1</field>
+ <field name="info">
+Synesthesia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="SYT14">
+ <field name="name">SYT14</field>
+ <field name="long_name">synaptotagmin XIV</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAC3">
+ <field name="name">TAC3</field>
+ <field name="long_name">tachykinin 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13-q21</field>
+ <field name="info">
+Hypogonadotropic hypogonadism [MIM:146110]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TACR3">
+ <field name="name">TACR3</field>
+ <field name="long_name">tachykinin receptor 3</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q25</field>
+ <field name="info">
+Hypogonadotropic hypogonadism [MIM:146110]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TACSTD2">
+ <field name="name">TACSTD2</field>
+ <field name="long_name">tumor-associated calcium signal transducer 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+Corneal dystrophy, gelatinous drop-like [MIM:204870]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAF15">
+ <field name="name">TAF15</field>
+ <field name="long_name">TAF15 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 68kDa</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.1-q11.2</field>
+ <field name="info">
+Chondrosarcoma, extraskeletal myxoid [MIM:612237]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAF1">
+ <field name="name">TAF1</field>
+ <field name="long_name">TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13</field>
+ <field name="info">
+Dystonia-Parkinsonism, X-linked [MIM:314250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAF7L">
+ <field name="name">TAF7L</field>
+ <field name="long_name">TAF7-like RNA polymerase II, TATA box binding protein (TBP)-associated factor, 50kDa</field>
+ <field name="chromosome">X</field>
+ <field name="location">X</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAL1">
+ <field name="name">TAL1</field>
+ <field name="long_name">T-cell acute lymphocytic leukemia 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32</field>
+ <field name="info">
+Leukemia-1, T-cell acute lymphocytic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAL2">
+ <field name="name">TAL2</field>
+ <field name="long_name">T-cell acute lymphocytic leukemia 2</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q31</field>
+ <field name="info">
+Leukemia-2, T-cell acute lymphoblastic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TALDO1">
+ <field name="name">TALDO1</field>
+ <field name="long_name">transaldolase 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5-p15.4</field>
+ <field name="info">
+Transaldolase deficiency [MIM:606003]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAM">
+ <field name="name">TAM</field>
+ <field name="long_name">Myeloproliferative syndrome, transient (transient abnormal</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q11.2</field>
+ <field name="info">
+Leukemia, transient, of Down syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAP1">
+ <field name="name">TAP1</field>
+ <field name="long_name">transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Bare lymphocyte syndrome, type I [MIM:604571]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAP2">
+ <field name="name">TAP2</field>
+ <field name="long_name">transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Bare lymphocyte syndrome, type I, due to TAP2 deficiency [MIM:604571]
+Wegener-like granulomatosis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAPBP">
+ <field name="name">TAPBP</field>
+ <field name="long_name">TAP binding protein (tapasin)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Bare lymphocyte syndrome, type I [MIM:604571]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAPVR1">
+ <field name="name">TAPVR1</field>
+ <field name="long_name">total anomalous pulmonary venous return 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q12</field>
+ <field name="info">
+Total anomalous pulmonary venous return</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TARDBP">
+ <field name="name">TARDBP</field>
+ <field name="long_name">TAR DNA binding protein</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.2</field>
+ <field name="info">
+Amyotrophic lateral sclerosis 10 [MIM:612069]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TARPS">
+ <field name="name">TARPS</field>
+ <field name="long_name">Talipes equinovarus, atrial septal defect, Robin sequence, and persistence of left superior vena cava</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23-q13.3</field>
+ <field name="info">
+TARP syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TARP">
+ <field name="name">TARP</field>
+ <field name="long_name">TCR gamma alternate reading frame protein</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23-q13.3</field>
+ <field name="info">
+TARP syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAR">
+ <field name="name">TAR</field>
+ <field name="long_name">Thrombocytopenia-absent radius syndrome</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q21.1</field>
+ <field name="info">
+Thrombocytopenia-absent radius syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAS2R16">
+ <field name="name">TAS2R16</field>
+ <field name="long_name">taste receptor, type 2, member 16</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAS2R38">
+ <field name="name">TAS2R38</field>
+ <field name="long_name">taste receptor, type 2, member 38</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q35-q36</field>
+ <field name="info">
+Phenylthiocarbamide tasting [MIM:171200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAS2R50">
+ <field name="name">TAS2R50</field>
+ <field name="long_name">taste receptor, type 2, member 50</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAT">
+ <field name="name">TAT</field>
+ <field name="long_name">tyrosine aminotransferase</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22.1-q22.3</field>
+ <field name="info">
+Tyrosinemia, type II</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TAZ">
+ <field name="name">TAZ</field>
+ <field name="long_name">tafazzin</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q24</field>
+ <field name="info">
+Dilated Cardiomyopathy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBC1D1">
+ <field name="name">TBC1D1</field>
+ <field name="long_name">TBC1 (tre-2/USP6, BUB2, cdc16) domain family, member 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p15.1-q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBCE">
+ <field name="name">TBCE</field>
+ <field name="long_name">tubulin folding cofactor E</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q42-q43</field>
+ <field name="info">
+Kenny-Caffey syndrome-1 [MIM:244460]
+Hypoparathyroidism-retardation-dysmorphism syndrome [MIM:241410]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBL1X">
+ <field name="name">TBL1X</field>
+ <field name="long_name">transducin (beta)-like 1X-linked</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBP">
+ <field name="name">TBP</field>
+ <field name="long_name">TATA box binding protein</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q27</field>
+ <field name="info">
+Spinocerebellar ataxia 17 [MIM:607136]
+Parkinson disease [MIM:168600]
+Huntington disease-like-4 [MIM:607136]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBX10">
+ <field name="name">TBX10</field>
+ <field name="long_name">T-box 10</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.1-q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBX15">
+ <field name="name">TBX15</field>
+ <field name="long_name">T-box 15</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13</field>
+ <field name="info">
+Cousin syndrome [MIM:260660]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBX1">
+ <field name="name">TBX1</field>
+ <field name="long_name">T-box 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+Conotruncal anomaly face syndrome [MIM:217095]
+DiGeorge syndrome [MIM:188400]
+Velocardiofacial syndrome [MIM:192430]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBX20">
+ <field name="name">TBX20</field>
+ <field name="long_name">T-box 20</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p15-p14</field>
+ <field name="info">
+Atrial septal defect 4 [MIM:611363]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBX21">
+ <field name="name">TBX21</field>
+ <field name="long_name">T-box 21</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.3</field>
+ <field name="info">
+Asthma, aspirin-induced, susceptibility to [MIM:208550]
+Asthma and nasal polyps [MIM:208550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBX22">
+ <field name="name">TBX22</field>
+ <field name="long_name">T-box 22</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq12-q21</field>
+ <field name="info">
+Cleft palate with ankyloglossia [MIM:303400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBX3">
+ <field name="name">TBX3</field>
+ <field name="long_name">T-box 3</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.1</field>
+ <field name="info">
+Ulnar-mammary syndrome [MIM:181450]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBX4">
+ <field name="name">TBX4</field>
+ <field name="long_name">T-box 4</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+Small patella syndrome [MIM:147891]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBX5">
+ <field name="name">TBX5</field>
+ <field name="long_name">T-box 5</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.1</field>
+ <field name="info">
+Holt-Oram syndrome [MIM:142900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBXA2R">
+ <field name="name">TBXA2R</field>
+ <field name="long_name">thromboxane A2 receptor</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Bleeding disorder due to defective thromboxane A2 receptor</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TBXAS1">
+ <field name="name">TBXAS1</field>
+ <field name="long_name">thromboxane A synthase 1 (platelet)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q34</field>
+ <field name="info">
+Thromboxane synthase deficiency
+Ghosal syndrome [MIM:231095]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCAP">
+ <field name="name">TCAP</field>
+ <field name="long_name">titin-cap (telethonin)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12</field>
+ <field name="info">
+Muscular dystrophy, limb-girdle, type 2G [MIM:601954]
+Cardiomyopathy, dilated, 1N [MIM:607487]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCF21">
+ <field name="name">TCF21</field>
+ <field name="long_name">transcription factor 21</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23-q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCF3">
+ <field name="name">TCF3</field>
+ <field name="long_name">transcription factor 3 (E2A immunoglobulin enhancer binding factors E12/E47)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+Leukemia, acute lymphoblastic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCF4">
+ <field name="name">TCF4</field>
+ <field name="long_name">transcription factor 4</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q21.1</field>
+ <field name="info">
+Pitt-Hopkins syndrome [MIM:610954]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCF7L2">
+ <field name="name">TCF7L2</field>
+ <field name="long_name">transcription factor 7-like 2 (T-cell specific, HMG-box)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q25.3</field>
+ <field name="info">
+Diabetes mellitus, type 2, susceptibility to [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCF7">
+ <field name="name">TCF7</field>
+ <field name="long_name">transcription factor 7 (T-cell specific, HMG-box)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCIRG1">
+ <field name="name">TCIRG1</field>
+ <field name="long_name">T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.4-q13.5</field>
+ <field name="info">
+Osteopetrosis, recessive 1 [MIM:259700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCL1A">
+ <field name="name">TCL1A</field>
+ <field name="long_name">T-cell leukemia/lymphoma 1A</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.1</field>
+ <field name="info">
+Leukemia/lymphoma, T-cell</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCL1B">
+ <field name="name">TCL1B</field>
+ <field name="long_name">T-cell leukemia/lymphoma 1B</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.1</field>
+ <field name="info">
+Leukemia/lymphoma, T-cell</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCL4">
+ <field name="name">TCL4</field>
+ <field name="long_name">T-cell leukemia/lymphoma 4</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q34</field>
+ <field name="info">
+Leukemia/lymphoma, T-cell</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCN2">
+ <field name="name">TCN2</field>
+ <field name="long_name">transcobalamin II; macrocytic anemia</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2-qter</field>
+ <field name="info">
+Transcobalamin II deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCOF1">
+ <field name="name">TCOF1</field>
+ <field name="long_name">Treacher Collins-Franceschetti syndrome 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q32-q33.1</field>
+ <field name="info">
+Treacher Collins mandibulofacial dysostosis [MIM:154500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCO">
+ <field name="name">TCO</field>
+ <field name="long_name">Thyroid carcinoma, nonmedullary, with cell oxyphilia</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2</field>
+ <field name="info">
+Thyroid carcinoma, nonmedullary, with cell oxyphilia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCP1">
+ <field name="name">TCP1</field>
+ <field name="long_name">t-complex 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25.3-q26</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TCPT">
+ <field name="name">TCPT</field>
+ <field name="long_name">thrombocytopenia, Paris-Trousseau type</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Thrombocytopenia, Paris-Trousseau type</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TDFA">
+ <field name="name">TDFA</field>
+ <field name="long_name">Testis-determining factor, autosomal (ZFY-related autosomal)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p24</field>
+ <field name="info">
+XY sex reversal</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TDF">
+ <field name="name">TDF</field>
+ <field name="long_name">tumor differentiation factor</field>
+ <field name="chromosome">Y</field>
+ <field name="location">Yp11.3</field>
+ <field name="info">
+Gonadal dysgenesis, XY female type [MIM:306100]
+Hermaphroditism, true [MIM:235600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TDGF1">
+ <field name="name">TDGF1</field>
+ <field name="long_name">teratocarcinoma-derived growth factor 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p23-p21</field>
+ <field name="info">
+Forebrain defects</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TDO2">
+ <field name="name">TDO2</field>
+ <field name="long_name">tryptophan 2,3-dioxygenase</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q31-q32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TDP1">
+ <field name="name">TDP1</field>
+ <field name="long_name">tyrosyl-DNA phosphodiesterase 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q31-q32</field>
+ <field name="info">
+Spinocerebellar ataxia, autosomal recessive with axonal neuropathy [MIM:607250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TEAD1">
+ <field name="name">TEAD1</field>
+ <field name="long_name">TEA domain family member 1 (SV40 transcriptional enhancer factor)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.2</field>
+ <field name="info">
+Sveinsson choreoretinal atrophy [MIM:108985]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TECTA">
+ <field name="name">TECTA</field>
+ <field name="long_name">tectorin alpha</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q22-q24</field>
+ <field name="info">
+Deafness, autosomal dominant 8/12 [MIM:601543]
+Deafness, autosomal recessive 21 [MIM:603629]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TEK">
+ <field name="name">TEK</field>
+ <field name="long_name">TEK tyrosine kinase, endothelial</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21</field>
+ <field name="info">
+Venous malformations, multiple cutaneous and mucosal [MIM:600195]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TELM">
+ <field name="name">TELM</field>
+ <field name="long_name">telomere length, mean leukocyte</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q23.2</field>
+ <field name="info">
+Telomere length, mean leukocyte</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TERC">
+ <field name="name">TERC</field>
+ <field name="long_name">telomerase RNA component</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21-q28</field>
+ <field name="info">
+Dyskeratosis congenita, autosomal dominant [MIM:127550]
+Aplastic anemia [MIM:609135]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TERT">
+ <field name="name">TERT</field>
+ <field name="long_name">telomerase reverse transcriptase</field>
+ <field name="chromosome">5</field>
+ <field name="location">5p15.33</field>
+ <field name="info">
+Aplastic anemia, susceptibility to [MIM:609135]
+Pulmonary fibrosis,idiopathic, susceptibility to [MIM:178500]
+Dyskeratosis congenita [MIM:127550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TEX14">
+ <field name="name">TEX14</field>
+ <field name="long_name">testis expressed 14</field>
+ <field name="chromosome">17</field>
+ <field name="location">17</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TFAM">
+ <field name="name">TFAM</field>
+ <field name="long_name">transcription factor A, mitochondrial</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TFAP2A">
+ <field name="name">TFAP2A</field>
+ <field name="long_name">transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p24</field>
+ <field name="info">
+Branchiooculofacial syndrome [MIM:113620]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TFAP2B">
+ <field name="name">TFAP2B</field>
+ <field name="long_name">transcription factor AP-2 beta (activating enhancer binding protein 2 beta)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p12</field>
+ <field name="info">
+Char syndrome [MIM:169100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TFCP2">
+ <field name="name">TFCP2</field>
+ <field name="long_name">transcription factor CP2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TFE3">
+ <field name="name">TFE3</field>
+ <field name="long_name">transcription factor binding to IGHM enhancer 3</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.22</field>
+ <field name="info">
+Renal cell carcinoma, papillary, 1 [MIM:605074]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TFG">
+ <field name="name">TFG</field>
+ <field name="long_name">TRK-fused gene</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q11-q12</field>
+ <field name="info">
+Chondrosarcoma, extraskeletal myxoid [MIM:612237]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TFPI">
+ <field name="name">TFPI</field>
+ <field name="long_name">tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31-q32.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TFR2">
+ <field name="name">TFR2</field>
+ <field name="long_name">transferrin receptor 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q22</field>
+ <field name="info">
+Hemochromatosis, type 3 [MIM:604250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TFRC">
+ <field name="name">TFRC</field>
+ <field name="long_name">transferrin receptor (p90, CD71)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q29</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TF">
+ <field name="name">TF</field>
+ <field name="long_name">transferrin</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21</field>
+ <field name="info">
+Atransferrinemia [MIM:209300]
+Iron deficiency anemia, susceptibility to (3) 9</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TGCT1">
+ <field name="name">TGCT1</field>
+ <field name="long_name">testicular germ cell tumor susceptibility 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq27</field>
+ <field name="info">
+Testicular germ cell tumor</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TGFB1">
+ <field name="name">TGFB1</field>
+ <field name="long_name">transforming growth factor, beta 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+Camurati-Engelmann disease [MIM:131300]
+Cystic fibrosis lung disease, modifier of [MIM:219700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TGFB2">
+ <field name="name">TGFB2</field>
+ <field name="long_name">transforming growth factor, beta 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q41</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TGFB3">
+ <field name="name">TGFB3</field>
+ <field name="long_name">transforming growth factor, beta 3</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24</field>
+ <field name="info">
+Arrhythmogenic right ventricular dysplasia 1 [MIM:107970]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TGFBI">
+ <field name="name">TGFBI</field>
+ <field name="long_name">transforming growth factor, beta-induced, 68kDa</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31</field>
+ <field name="info">
+Corneal dystrophy, Groenouw type I [MIM:121900]
+Corneal dystrophy, lattice type I [MIM:122200]
+Corneal dystrophy, Reis-Bucklers type [MIM:608470]
+Corneal dystrophy, Avellino type [MIM:607541]
+Corneal dystrophy, lattice type IIIA [MIM:608471]
+Corneal dystrophy, Thiel-Behnke type [MIM:602082]
+Corneal dystrophy, epithelial basement membrane [MIM:121820]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TGFBR1">
+ <field name="name">TGFBR1</field>
+ <field name="long_name">transforming growth factor, beta receptor 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22</field>
+ <field name="info">
+Loeys-Dietz syndrome, type 1A [MIM:609129]
+Loeys-Dietz syndrome, type 2A [MIM:608967]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TGFBR2">
+ <field name="name">TGFBR2</field>
+ <field name="long_name">transforming growth factor, beta receptor II (70/80kDa)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p22</field>
+ <field name="info">
+Colorectal cancer, hereditary nonpolyposis, type 6
+Esophageal cancer [MIM:133239]
+Loeys-Dietz syndrome, type 1B [MIM:610168]
+Loeys-Dietz syndrome, type 2B [MIM:610380]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TGFBR3">
+ <field name="name">TGFBR3</field>
+ <field name="long_name">transforming growth factor, beta receptor III</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p33-p32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TGM1">
+ <field name="name">TGM1</field>
+ <field name="long_name">transglutaminase 1 (K polypeptide epidermal type I, protein-glutamine-gamma-glutamyltransferase)</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2</field>
+ <field name="info">
+Ichthyosis, lamellar, autosomal recessive [MIM:242300]
+Ichthyosiform erythroderma, congenital [MIM:242100]
+Self-healing collodion baby [MIM:242300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TGM2">
+ <field name="name">TGM2</field>
+ <field name="long_name">transglutaminase 2 (C polypeptide, protein-glutamine-gamma-glutamyltransferase)</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q11.2-q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TGM6">
+ <field name="name">TGM6</field>
+ <field name="long_name">transglutaminase 6</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15.2</field>
+ <field name="info">
+Peeling skin syndrome, acral type [MIM:609796]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TG">
+ <field name="name">TG</field>
+ <field name="long_name">thyroglobulin</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.2-q24.3</field>
+ <field name="info">
+Hypothyroidism, hereditary congenital
+Goiter, adolescent multinodular
+Goiter, nonendemic, simple
+Autoimmune thyroid disease, susceptibility to 3 [MIM:608175]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="THAP1">
+ <field name="name">THAP1</field>
+ <field name="long_name">THAP domain containing, apoptosis associated protein 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p11.21</field>
+ <field name="info">
+Dystonia 6, torsion [MIM:602629]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="THAS">
+ <field name="name">THAS</field>
+ <field name="long_name">thoracoabdominal syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq25-q26.1</field>
+ <field name="info">
+Thoracoabdominal syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="THBD">
+ <field name="name">THBD</field>
+ <field name="long_name">thrombomodulin</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p11.2</field>
+ <field name="info">
+Thrombophilia due to thrombomodulin defect
+Myocardial infarction, susceptibility to (3) 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="THBS1">
+ <field name="name">THBS1</field>
+ <field name="long_name">thrombospondin 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="THBS2">
+ <field name="name">THBS2</field>
+ <field name="long_name">thrombospondin 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q27</field>
+ <field name="info">
+Lumbar disc herniation, susceptibility to [MIM:603932]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="THC2">
+ <field name="name">THC2</field>
+ <field name="long_name">thrombocytopenia 2 (autosomal dominant)</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p12.1</field>
+ <field name="info">
+Thrombocytopenia-2 [MIM:188000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="THM">
+ <field name="name">THM</field>
+ <field name="long_name">thymoma</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.1</field>
+ <field name="info">
+Tibial hemimelia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="THPO">
+ <field name="name">THPO</field>
+ <field name="long_name">thrombopoietin</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q26.3-q27</field>
+ <field name="info">
+Thrombocythemia, essential [MIM:187950]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="THRA">
+ <field name="name">THRA</field>
+ <field name="long_name">thyroid hormone receptor, alpha (erythroblastic leukemia viral (v-erb-a) oncogene homolog, avian)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2</field>
+ <field name="info">
+Pituitary adenoma, nonfunctioning</field>
+</record>
+<record model="gnuhealth.disease.gene" id="THRB">
+ <field name="name">THRB</field>
+ <field name="long_name">thyroid hormone receptor, beta (erythroblastic leukemia viral (v-erb-a) oncogene homolog 2, avian)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p24.3</field>
+ <field name="info">
+Thyroid hormone resistance [MIM:188570]
+Thyroid hormone resistance, autosomal recessive [MIM:274300]
+Thyroid hromone resistance, selective pituitary [MIM:145650]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TH">
+ <field name="name">TH</field>
+ <field name="long_name">tyrosine hydroxylase</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Segawa syndrome, recessive [MIM:605407]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TIMM44">
+ <field name="name">TIMM44</field>
+ <field name="long_name">translocase of inner mitochondrial membrane 44 homolog (yeast)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3-p13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TIMM8A">
+ <field name="name">TIMM8A</field>
+ <field name="long_name">translocase of inner mitochondrial membrane 8 homolog A (yeast)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq22</field>
+ <field name="info">
+Deafness, X-linked 1, progressive
+Mohr-Tranebjaerg syndrome [MIM:304700]
+Jensen syndrome [MIM:311150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TIMP1">
+ <field name="name">TIMP1</field>
+ <field name="long_name">TIMP metallopeptidase inhibitor 1</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.3-p11.23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TIMP2">
+ <field name="name">TIMP2</field>
+ <field name="long_name">TIMP metallopeptidase inhibitor 2</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TIMP3">
+ <field name="name">TIMP3</field>
+ <field name="long_name">TIMP metallopeptidase inhibitor 3</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12.1-q13.2</field>
+ <field name="info">
+Sorsby fundus dystrophy [MIM:136900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TINF2">
+ <field name="name">TINF2</field>
+ <field name="long_name">TERF1 (TRF1)-interacting nuclear factor 2</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q12</field>
+ <field name="info">
+Dyskeratosis congenita, autosomal dominant [MIM:127550]
+Revesz syndrome [MIM:268130]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TIRAP">
+ <field name="name">TIRAP</field>
+ <field name="long_name">toll-interleukin 1 receptor (TIR) domain containing adaptor protein</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23-q24</field>
+ <field name="info">
+Pneumococcal disease, invasive, protection against [MIM:610799]
+Bacteremia, protection against
+Malaria, protection against [MIM:611162]
+Tuberculosis, protection against [MIM:607948]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TJP2">
+ <field name="name">TJP2</field>
+ <field name="long_name">tight junction protein 2 (zona occludens 2)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q12-q13</field>
+ <field name="info">
+Hypercholanemia, familial [MIM:607748]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TK2">
+ <field name="name">TK2</field>
+ <field name="long_name">thymidine kinase 2, mitochondrial</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22</field>
+ <field name="info">
+Mitochondrial DNA depletion syndrome, myopathic form [MIM:609560]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TKCR">
+ <field name="name">TKCR</field>
+ <field name="long_name">torticollis, keloids, cryptorchidism and renal dysplasia</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Goeminne TKCR syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TLL1">
+ <field name="name">TLL1</field>
+ <field name="long_name">tolloid-like 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q32-q33</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TLR1">
+ <field name="name">TLR1</field>
+ <field name="long_name">toll-like receptor 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p14</field>
+ <field name="info">
+Leprosy, protection against [MIM:246300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TLR2">
+ <field name="name">TLR2</field>
+ <field name="long_name">toll-like receptor 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q32</field>
+ <field name="info">
+Leprosy, susceptibility to [MIM:246300]
+Colorectal cancer, susceptibility to [MIM:114500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TLR3">
+ <field name="name">TLR3</field>
+ <field name="long_name">toll-like receptor 3</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q35</field>
+ <field name="info">
+Herpes simplex encephalitis, TLR3-deficient, susceptibility to
+Geographic atrophy, susceptibility to progression to, in age-related macular degeneration [MIM:612479]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TLR4">
+ <field name="name">TLR4</field>
+ <field name="long_name">toll-like receptor 4</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q32-q33</field>
+ <field name="info">
+Endotoxin hyporesponsiveness
+Macular degeneration, age-related, 10 [MIM:611488]
+Colorectal cancer, susceptibility to [MIM:114500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TLR5">
+ <field name="name">TLR5</field>
+ <field name="long_name">toll-like receptor 5</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q41-q42</field>
+ <field name="info">
+Legionaire disease, susceptibility to [MIM:608556]
+Systemic lupus erythematosus, resistance to [MIM:601744]
+Systemic lupus erythematosus, susceptibility to, 1 [MIM:601744]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TLR6">
+ <field name="name">TLR6</field>
+ <field name="long_name">toll-like receptor 6</field>
+ <field name="chromosome">4</field>
+ <field name="location">4</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TLR9">
+ <field name="name">TLR9</field>
+ <field name="long_name">toll-like receptor 9</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TLX1">
+ <field name="name">TLX1</field>
+ <field name="long_name">T-cell leukemia homeobox 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24</field>
+ <field name="info">
+Leukemia, T-cell acute lymphocytic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TMC1">
+ <field name="name">TMC1</field>
+ <field name="long_name">transmembrane channel-like 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q13-q21</field>
+ <field name="info">
+Deafness, autosomal recessive 7 [MIM:600974]
+Deafness, autosomal dominant 36 [MIM:606705]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TMEM114">
+ <field name="name">TMEM114</field>
+ <field name="long_name">transmembrane protein 114</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TMEM43">
+ <field name="name">TMEM43</field>
+ <field name="long_name">transmembrane protein 43</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25</field>
+ <field name="info">
+Arrhythmogenic right ventricular dysplasia, familial, 5 [MIM:604400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TMEM67">
+ <field name="name">TMEM67</field>
+ <field name="long_name">transmembrane protein 67</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21.13-q22.1</field>
+ <field name="info">
+Meckel syndrome, type 3 [MIM:607361]
+Joubert syndrome 6 [MIM:610688]
+Bardet-Biedl syndrome 14, modifier of [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TMEM70">
+ <field name="name">TMEM70</field>
+ <field name="long_name">transmembrane protein 70</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21.11</field>
+ <field name="info">
+Encephalocardiomyopathy, neonatal, mitochondrial, due to ATP synthase deficiency [MIM:604273]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TMIE">
+ <field name="name">TMIE</field>
+ <field name="long_name">transmembrane inner ear</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21</field>
+ <field name="info">
+Deafness, autosomal recessive 6 [MIM:600971]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TMPO">
+ <field name="name">TMPO</field>
+ <field name="long_name">thymopoietin</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q22</field>
+ <field name="info">
+Cardiomyopathy, dilated, 1T</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TMPRSS11A">
+ <field name="name">TMPRSS11A</field>
+ <field name="long_name">transmembrane protease, serine 11A</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TMPRSS3">
+ <field name="name">TMPRSS3</field>
+ <field name="long_name">transmembrane protease, serine 3</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+Deafness, autosomal recessive 8, childhood onset [MIM:601072]
+Deafness, autosomal recessive 10, congenital [MIM:605316]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TMPRSS4">
+ <field name="name">TMPRSS4</field>
+ <field name="long_name">transmembrane protease, serine 4</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TMPRSS5">
+ <field name="name">TMPRSS5</field>
+ <field name="long_name">transmembrane protease, serine 5</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TMPRSS6">
+ <field name="name">TMPRSS6</field>
+ <field name="long_name">transmembrane protease, serine 6</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12-q13</field>
+ <field name="info">
+Iron-refractory iron deficiency anemia [MIM:206200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNC">
+ <field name="name">TNC</field>
+ <field name="long_name">tenascin C</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q33</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNDM">
+ <field name="name">TNDM</field>
+ <field name="long_name">diabetes mellitus, transient neonatal</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q24</field>
+ <field name="info">
+Diabetes mellitus, transient neonatal [MIM:601410]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFAIP3">
+ <field name="name">TNFAIP3</field>
+ <field name="long_name">tumor necrosis factor, alpha-induced protein 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFRSF10B">
+ <field name="name">TNFRSF10B</field>
+ <field name="long_name">tumor necrosis factor receptor superfamily, member 10b</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p22-p21</field>
+ <field name="info">
+Squamous cell carcinoma, head and neck [MIM:275355]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFRSF11A">
+ <field name="name">TNFRSF11A</field>
+ <field name="long_name">tumor necrosis factor receptor superfamily, member 11a, NFKB activator</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q22.1</field>
+ <field name="info">
+Osteolysis, familial expansile [MIM:174810]
+Paget disease of bone [MIM:602080]
+Osteopetrosis, autosomal recessive 7 [MIM:612301]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFRSF11B">
+ <field name="name">TNFRSF11B</field>
+ <field name="long_name">tumor necrosis factor receptor superfamily, member 11b</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24</field>
+ <field name="info">
+Paget disease, juvenile [MIM:239000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFRSF13B">
+ <field name="name">TNFRSF13B</field>
+ <field name="long_name">tumor necrosis factor receptor superfamily, member 13B</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p11.2</field>
+ <field name="info">
+Immunoglobulin A deficiency [MIM:609529]
+Common variable immunodeficiency [MIM:240500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFRSF13C">
+ <field name="name">TNFRSF13C</field>
+ <field name="long_name">tumor necrosis factor receptor superfamily, member 13C</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.1-q13.31</field>
+ <field name="info">
+Common Variable Immune Deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFRSF1A">
+ <field name="name">TNFRSF1A</field>
+ <field name="long_name">tumor necrosis factor receptor superfamily, member 1A</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.2</field>
+ <field name="info">
+Periodic fever, familial [MIM:142680]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFRSF1B">
+ <field name="name">TNFRSF1B</field>
+ <field name="long_name">tumor necrosis factor receptor superfamily, member 1B</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3-p36.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFRSF25">
+ <field name="name">TNFRSF25</field>
+ <field name="long_name">tumor necrosis factor receptor superfamily, member 25</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFRSF4">
+ <field name="name">TNFRSF4</field>
+ <field name="long_name">tumor necrosis factor receptor superfamily, member 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFSF11">
+ <field name="name">TNFSF11</field>
+ <field name="long_name">tumor necrosis factor (ligand) superfamily, member 11</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q14</field>
+ <field name="info">
+Osteopetrosis, autosomal recessive 2 [MIM:259710]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFSF13B">
+ <field name="name">TNFSF13B</field>
+ <field name="long_name">tumor necrosis factor (ligand) superfamily, member 13b</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q32-q34</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFSF14">
+ <field name="name">TNFSF14</field>
+ <field name="long_name">tumor necrosis factor (ligand) superfamily, member 14</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFSF15">
+ <field name="name">TNFSF15</field>
+ <field name="long_name">tumor necrosis factor (ligand) superfamily, member 15</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNFSF4">
+ <field name="name">TNFSF4</field>
+ <field name="long_name">tumor necrosis factor (ligand) superfamily, member 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q25</field>
+ <field name="info">
+Myocardial infarction, susceptibility to [MIM:608446]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNF">
+ <field name="name">TNF</field>
+ <field name="long_name">tumor necrosis factor (TNF superfamily, member 2)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Malaria, cerebral, susceptibility to [MIM:611162]
+Septic shock, susceptibility to
+Asthma, susceptibility to [MIM:600807]
+Dementia, vascular, susceptibility to
+Migraine without aura, susceptibility to [MIM:157300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNNC1">
+ <field name="name">TNNC1</field>
+ <field name="long_name">troponin C type 1 (slow)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.3-p14.3</field>
+ <field name="info">
+Cardiomyopathy, dilated, 1Z [MIM:611879]
+Cardiomyopathy, familial hypertrophic [MIM:192600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNNI2">
+ <field name="name">TNNI2</field>
+ <field name="long_name">troponin I type 2 (skeletal, fast)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Arthrogryposis multiplex congenita, distal, type 2B [MIM:601680]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNNI3">
+ <field name="name">TNNI3</field>
+ <field name="long_name">troponin I type 3 (cardiac)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+Cardiomyopathy, familial hypertrophic, 7
+Cardiomyopathy, familial restrictive [MIM:115210]
+Cardiomyopathy, dilated, 2A [MIM:611880]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNNT1">
+ <field name="name">TNNT1</field>
+ <field name="long_name">troponin T type 1 (skeletal, slow)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+Nemaline myopathy, Amish type [MIM:605355]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNNT2">
+ <field name="name">TNNT2</field>
+ <field name="long_name">troponin T type 2 (cardiac)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32</field>
+ <field name="info">
+Cardiomyopathy, familial hypertrophic, 2 [MIM:115195]
+Cardiomyopathy, dilated, 1D [MIM:601494]
+Cardiomyopathy, familial restrictive, 3 [MIM:612422]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNNT3">
+ <field name="name">TNNT3</field>
+ <field name="long_name">troponin T type 3 (skeletal, fast)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Arthyrgryposis, distal, type 2B [MIM:601680]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNP1">
+ <field name="name">TNP1</field>
+ <field name="long_name">transition protein 1 (during histone to protamine replacement)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35-q36</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNS3">
+ <field name="name">TNS3</field>
+ <field name="long_name">tensin 3</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p12.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TNXB">
+ <field name="name">TNXB</field>
+ <field name="long_name">tenascin XB</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Ehlers-Danlos due to tenascin X deficiency [MIM:606408]
+Ehlers-Danlos syndrome, hypermobility type [MIM:130020]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TOC">
+ <field name="name">TOC</field>
+ <field name="long_name">tylosis with oesophageal cancer</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25</field>
+ <field name="info">
+Tylosis with esophageal cancer</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TOMM40">
+ <field name="name">TOMM40</field>
+ <field name="long_name">translocase of outer mitochondrial membrane 40 homolog (yeast)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TOP1MT">
+ <field name="name">TOP1MT</field>
+ <field name="long_name">topoisomerase (DNA) I, mitochondrial</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TOP1">
+ <field name="name">TOP1</field>
+ <field name="long_name">topoisomerase (DNA) I</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q12-q13.1</field>
+ <field name="info">
+DNA topoisomerase I, camptothecin-resistant</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TOP2A">
+ <field name="name">TOP2A</field>
+ <field name="long_name">topoisomerase (DNA) II alpha 170kDa</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+DNA topoisomerase II, resistance to inhibition of, by amsacrine</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TOPBP1">
+ <field name="name">TOPBP1</field>
+ <field name="long_name">topoisomerase (DNA) II binding protein 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TOPORS">
+ <field name="name">TOPORS</field>
+ <field name="long_name">topoisomerase I binding, arginine/serine-rich</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p21</field>
+ <field name="info">
+Retinitis pigmentosa-31 [MIM:609923]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TOR1A">
+ <field name="name">TOR1A</field>
+ <field name="long_name">torsin family 1, member A (torsin A)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+Early-Onset Primary Dystonia (DYT1)</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TP53BP1">
+ <field name="name">TP53BP1</field>
+ <field name="long_name">tumor protein p53 binding protein 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15-q21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TP53">
+ <field name="name">TP53</field>
+ <field name="long_name">tumor protein p53</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.1</field>
+ <field name="info">
+Colorectal cancer [MIM:114500]
+Li-Fraumeni syndrome [MIM:151623]
+Hepatocellular carcinoma [MIM:114550]
+Osteosarcoma [MIM:259500]
+Choroid plexus papilloma [MIM:260500]
+Nasopharyngeal carcinoma [MIM:161550]
+Pancreatic cancer [MIM:260350]
+Adrenal cortical carcinoma [MIM:202300]
+Breast cancer [MIM:114480]
+Li-Fraumeni-like syndrome [MIM:151623]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TP63">
+ <field name="name">TP63</field>
+ <field name="long_name">tumor protein p63</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q27</field>
+ <field name="info">
+Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 [MIM:604292]
+Split-hand/foot malformation, type 4 [MIM:605289]
+Hay-Wells syndrome [MIM:106260]
+ADULT syndrome [MIM:103285]
+Limb-mammary syndrome [MIM:603543]
+Rapp-Hodgkin syndrome [MIM:129400]
+Orofacial cleft 8 [MIM:129400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TP73">
+ <field name="name">TP73</field>
+ <field name="long_name">tumor protein p73</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36</field>
+ <field name="info">
+Neuroblastoma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TPCN2">
+ <field name="name">TPCN2</field>
+ <field name="long_name">two pore segment channel 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13.2</field>
+ <field name="info">
+Skin/hair/eye pigmentation 10, blond/brown hair [MIM:612267]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TPH1">
+ <field name="name">TPH1</field>
+ <field name="long_name">tryptophan hydroxylase 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.3-p14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TPH2">
+ <field name="name">TPH2</field>
+ <field name="long_name">tryptophan hydroxylase 2</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q21.1</field>
+ <field name="info">
+Unipolar depression, susceptibility to [MIM:608516]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TPI1">
+ <field name="name">TPI1</field>
+ <field name="long_name">triosephosphate isomerase 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+Hemolytic anemia due to triosephosphate isomerase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TPM1">
+ <field name="name">TPM1</field>
+ <field name="long_name">tropomyosin 1 (alpha)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22.1</field>
+ <field name="info">
+Cardiomyopathy, familial hypertrophic, 3 [MIM:115196]
+Cardiomyopathy, dilated, 1Y [MIM:611878]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TPM2">
+ <field name="name">TPM2</field>
+ <field name="long_name">tropomyosin 2 (beta)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p13.2-p13.1</field>
+ <field name="info">
+Arthrogryposis multiplex congenita, distal, type 1 [MIM:108120]
+Nemaline myopathy [MIM:161800]
+Arthrogryposis, distal, type 2B [MIM:601680]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TPM3">
+ <field name="name">TPM3</field>
+ <field name="long_name">tropomyosin 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q22-q23</field>
+ <field name="info">
+Nemaline myopathy 1, autosomal dominant [MIM:161800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TPMT">
+ <field name="name">TPMT</field>
+ <field name="long_name">thiopurine S-methyltransferase</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p22.3</field>
+ <field name="info">
+6-mercaptopurine sensitivity [MIM:610460]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TPO">
+ <field name="name">TPO</field>
+ <field name="long_name">thyroid peroxidase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p25</field>
+ <field name="info">
+Thyroid hormone organification defect IIA [MIM:274500]
+Goiter, congenital
+Hyperthyroidism, congenital
+Total iodide organification defect [MIM:274500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TPP1">
+ <field name="name">TPP1</field>
+ <field name="long_name">tripeptidyl peptidase I</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Ceroid-lipofuscinosis, neuronal 2, classic late infantile [MIM:204500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRADD">
+ <field name="name">TRADD</field>
+ <field name="long_name">TNFRSF1A-associated via death domain</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRAK2">
+ <field name="name">TRAK2</field>
+ <field name="long_name">trafficking protein, kinesin binding 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q33-q34</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRAPPC2">
+ <field name="name">TRAPPC2</field>
+ <field name="long_name">trafficking protein particle complex 2</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.2-p22.1</field>
+ <field name="info">
+Spondyloepiphyseal dysplasia tarda [MIM:313400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TREH">
+ <field name="name">TREH</field>
+ <field name="long_name">trehalase (brush-border membrane glycoprotein)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Trehalase deficiency [MIM:612119]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TREM2">
+ <field name="name">TREM2</field>
+ <field name="long_name">triggering receptor expressed on myeloid cells 2</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.2</field>
+ <field name="info">
+Nasu-Hakola disease [MIM:221770]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TREX1">
+ <field name="name">TREX1</field>
+ <field name="long_name">three prime repair exonuclease 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.3-p21.2</field>
+ <field name="info">
+Aicardi-Goutieres syndrome 1 [MIM:225750]
+Aicardi-Goutieres syndrome 5 [MIM:610905]
+Cree encephalitis [MIM:225750]
+Chilblain lupus [MIM:610448]
+Vasculopathy, retinal, with cerebral leukodystrophy [MIM:192315]
+Systemic lupus erythematosus, susceptibility to [MIM:152700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRHR">
+ <field name="name">TRHR</field>
+ <field name="long_name">thyrotropin-releasing hormone receptor</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q23</field>
+ <field name="info">
+Thyrotropin-releasing hormone resistance, generalized</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRH">
+ <field name="name">TRH</field>
+ <field name="long_name">thyrotropin-releasing hormone</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q13.3-q21</field>
+ <field name="info">
+Thyrotropin-releasing hormone deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRICY1">
+ <field name="name">TRICY1</field>
+ <field name="long_name">trichilemmal cyst 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p24-p21.2</field>
+ <field name="info">
+Trichilemmal cyst 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRIM21">
+ <field name="name">TRIM21</field>
+ <field name="long_name">tripartite motif-containing 21</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRIM24">
+ <field name="name">TRIM24</field>
+ <field name="long_name">tripartite motif-containing 24</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q32-q34</field>
+ <field name="info">
+Thyroid carcinoma, papillary [MIM:188550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRIM32">
+ <field name="name">TRIM32</field>
+ <field name="long_name">tripartite motif-containing 32</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q31-q34.1</field>
+ <field name="info">
+Muscular dystrophy, limb-girdle, type 2H [MIM:254110]
+Bardet-Biedl syndrome 11 [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRIM33">
+ <field name="name">TRIM33</field>
+ <field name="long_name">tripartite motif-containing 33</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13</field>
+ <field name="info">
+Thyroid carcinoma, papillary [MIM:188550]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRIM37">
+ <field name="name">TRIM37</field>
+ <field name="long_name">tripartite motif-containing 37</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q22-q23</field>
+ <field name="info">
+Mulibrey nanism [MIM:253250]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRIM5">
+ <field name="name">TRIM5</field>
+ <field name="long_name">tripartite motif-containing 5</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRIOBP">
+ <field name="name">TRIOBP</field>
+ <field name="long_name">TRIO and F-actin binding protein</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.1</field>
+ <field name="info">
+Deafness, autosomal recessive 28 [MIM:609823]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRMU">
+ <field name="name">TRMU</field>
+ <field name="long_name">tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13</field>
+ <field name="info">
+Deafness, mitochondrial, modifier of [MIM:580000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRNT1">
+ <field name="name">TRNT1</field>
+ <field name="long_name">tRNA nucleotidyl transferase, CCA-adding, 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13</field>
+ <field name="info">
+Deafness, mitochondrial, modifier of [MIM:580000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRO">
+ <field name="name">TRO</field>
+ <field name="long_name">trophinin</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.22-p11.21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRPC6">
+ <field name="name">TRPC6</field>
+ <field name="long_name">transient receptor potential cation channel, subfamily C, member 6</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q21-q22</field>
+ <field name="info">
+Glomerulosclerosis, focal segmental, 2 [MIM:603965]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRPM1">
+ <field name="name">TRPM1</field>
+ <field name="long_name">transient receptor potential cation channel, subfamily M, member 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q13-q14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRPM2">
+ <field name="name">TRPM2</field>
+ <field name="long_name">transient receptor potential cation channel, subfamily M, member 2</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRPM3">
+ <field name="name">TRPM3</field>
+ <field name="long_name">transient receptor potential cation channel, subfamily M, member 3</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q21.12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRPM6">
+ <field name="name">TRPM6</field>
+ <field name="long_name">transient receptor potential cation channel, subfamily M, member 6</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22</field>
+ <field name="info">
+Hypomagnesemia with secondary hypocalcemia [MIM:602014]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRPM7">
+ <field name="name">TRPM7</field>
+ <field name="long_name">transient receptor potential cation channel, subfamily M, member 7</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q21</field>
+ <field name="info">
+Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1, susceptibility to [MIM:105500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRPS1">
+ <field name="name">TRPS1</field>
+ <field name="long_name">trichorhinophalangeal syndrome I</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24.12</field>
+ <field name="info">
+Trichorhinophalangeal syndrome, type I [MIM:190350]
+Trichorhinophalangeal syndrome, type III [MIM:190351]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRPV1">
+ <field name="name">TRPV1</field>
+ <field name="long_name">transient receptor potential cation channel, subfamily V, member 1</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TRPV4">
+ <field name="name">TRPV4</field>
+ <field name="long_name">transient receptor potential cation channel, subfamily V, member 4</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q24.1</field>
+ <field name="info">
+Brachyolmia type 3 [MIM:113500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSC1">
+ <field name="name">TSC1</field>
+ <field name="long_name">tuberous sclerosis 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q34</field>
+ <field name="info">
+Tuberous sclerosis-1 [MIM:191100]
+Lymphangioleiomyomatosis [MIM:606690]
+Focal cortical dysplasia, Taylor balloon cell type [MIM:607341]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSC2">
+ <field name="name">TSC2</field>
+ <field name="long_name">tuberous sclerosis 2</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.3</field>
+ <field name="info">
+Tuberous sclerosis-2 [MIM:191100]
+Lymphangioleiomyomatosis, somatic [MIM:606690]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSEN2">
+ <field name="name">TSEN2</field>
+ <field name="long_name">tRNA splicing endonuclease 2 homolog (S. cerevisiae)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25.1</field>
+ <field name="info">
+Pontocerebellar hypoplasia type 2B [MIM:612389]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSEN34">
+ <field name="name">TSEN34</field>
+ <field name="long_name">tRNA splicing endonuclease 34 homolog (S. cerevisiae)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.4</field>
+ <field name="info">
+Pontocerebellar hypoplasia type 2C [MIM:612390]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSEN54">
+ <field name="name">TSEN54</field>
+ <field name="long_name">tRNA splicing endonuclease 54 homolog (S. cerevisiae)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25.1</field>
+ <field name="info">
+Pontocerebellar hypoplasia type 2A [MIM:277470]
+Pontocerebellar hypoplasia type 4 [MIM:225753]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSFM">
+ <field name="name">TSFM</field>
+ <field name="long_name">Ts translation elongation factor, mitochondrial</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13-q14</field>
+ <field name="info">
+Combined oxidative phosphorylation deficiency 3 [MIM:610505]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSG101">
+ <field name="name">TSG101</field>
+ <field name="long_name">tumor susceptibility gene 101</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.2-p15.1</field>
+ <field name="info">
+Breast cancer</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSG11">
+ <field name="name">TSG11</field>
+ <field name="long_name">Tumor suppressor gene on chromosome 11</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23</field>
+ <field name="info">
+Nonsmall cell lung cancer</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSHB">
+ <field name="name">TSHB</field>
+ <field name="long_name">thyroid stimulating hormone, beta</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13</field>
+ <field name="info">
+Hypothryoidism, congenital, nongoitrous 4 [MIM:275100]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSHQTL1">
+ <field name="name">TSHQTL1</field>
+ <field name="long_name">Thyroid-stimulating hormone level QTL 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13</field>
+ <field name="info">
+Thyroid-stimulating hormone level QTL 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSHR">
+ <field name="name">TSHR</field>
+ <field name="long_name">thyroid stimulating hormone receptor</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q31</field>
+ <field name="info">
+Hypothyroidism, congenital, nongoitrous, 1 [MIM:275200]
+Thyroid adenoma, hyperfunctioning, somatic
+Hyperthyroidism, nonautoimmune [MIM:609152]
+Thyroid carcinoma with thyrotoxicosis
+Hyperthyroidism, familial gestational [MIM:603373]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSLP">
+ <field name="name">TSLP</field>
+ <field name="long_name">thymic stromal lymphopoietin</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q22.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSPYL1">
+ <field name="name">TSPYL1</field>
+ <field name="long_name">TSPY-like 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q22-q23</field>
+ <field name="info">
+Sudden infant death with dysgenesis of the testes syndrome [MIM:608800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSSK3">
+ <field name="name">TSSK3</field>
+ <field name="long_name">testis-specific serine kinase 3</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p35-p34</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TSSK4">
+ <field name="name">TSSK4</field>
+ <field name="long_name">testis-specific serine kinase 4</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TST">
+ <field name="name">TST</field>
+ <field name="long_name">thiosulfate sulfurtransferase (rhodanese)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2-qter</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TTBK2">
+ <field name="name">TTBK2</field>
+ <field name="long_name">tau tubulin kinase 2</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15.2</field>
+ <field name="info">
+Spinocerebellar ataxia-11 [MIM:604432]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TTC8">
+ <field name="name">TTC8</field>
+ <field name="long_name">tetratricopeptide repeat domain 8</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.1</field>
+ <field name="info">
+Bardet-Biedl syndrome 8 [MIM:209900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TTF1">
+ <field name="name">TTF1</field>
+ <field name="long_name">transcription termination factor, RNA polymerase I</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q13</field>
+ <field name="info">
+Goiter, familial, due to TTF-1 defect
+Chorea, hereditary benign [MIM:118700]
+Choreoathetosis, hypothyroidism, and neonatal respiratory distress [MIM:610978]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TTF2">
+ <field name="name">TTF2</field>
+ <field name="long_name">transcription termination factor, RNA polymerase II</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22</field>
+ <field name="info">
+Bamforth-Lazarus syndrome [MIM:241850]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TTN">
+ <field name="name">TTN</field>
+ <field name="long_name">titin</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31</field>
+ <field name="info">
+Cardiomyopathy, familial hypertrophic, 9
+Cardiomyopathy, dilated, 1G [MIM:604145]
+Tibial muscular dystrophy, tardive [MIM:600334]
+Muscular dystrophy, limb-girdle, type 2J [MIM:608807]
+Myopathy, proximal, with early respiratory muscle involvement [MIM:603689]
+Myopathy, early-onset, with fatal cardiomyopathy [MIM:611705]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TTPA">
+ <field name="name">TTPA</field>
+ <field name="long_name">tocopherol (alpha) transfer protein</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q13.1-q13.3</field>
+ <field name="info">
+Ataxia with isolated vitamin E deficiency [MIM:277460]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TTR">
+ <field name="name">TTR</field>
+ <field name="long_name">transthyretin</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q11.2-q12.1</field>
+ <field name="info">
+Amyloid polyneuropathy, several types [MIM:105210]
+Dystransthyretinemic hyperthyroxinemia
+Amyloidosis, senile systemic
+Carpal tunnel syndrome, familial</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TUBA1A">
+ <field name="name">TUBA1A</field>
+ <field name="long_name">tubulin, alpha 1a</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q12-q14</field>
+ <field name="info">
+Lissencephaly 3 [MIM:611603]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TUFM">
+ <field name="name">TUFM</field>
+ <field name="long_name">Tu translation elongation factor, mitochondrial</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p11.2</field>
+ <field name="info">
+Combined oxidative phosphorylation deficiency 4 [MIM:610678]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TUKLS">
+ <field name="name">TUKLS</field>
+ <field name="long_name">Tukel syndrome</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q22</field>
+ <field name="info">
+Tukel syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TULP1">
+ <field name="name">TULP1</field>
+ <field name="long_name">tubby like protein 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Retinitis pigmentosa-14 [MIM:600132]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TUSC3">
+ <field name="name">TUSC3</field>
+ <field name="long_name">tumor suppressor candidate 3</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p22</field>
+ <field name="info">
+Mental retardation, autosomal recessive 7 [MIM:611093]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TXNDC3">
+ <field name="name">TXNDC3</field>
+ <field name="long_name">thioredoxin domain containing 3 (spermatozoa)</field>
+ <field name="chromosome">7</field>
+ <field name="location">7p14-p13</field>
+ <field name="info">
+Ciliary dyskinesia, primary, 6 [MIM:610852]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TYK2">
+ <field name="name">TYK2</field>
+ <field name="long_name">tyrosine kinase 2</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2</field>
+ <field name="info">
+Protein-tyrosine kinase 2 deficiency [MIM:611521]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TYMS">
+ <field name="name">TYMS</field>
+ <field name="long_name">thymidylate synthetase</field>
+ <field name="chromosome">18</field>
+ <field name="location">18p11.32</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="TYROBP">
+ <field name="name">TYROBP</field>
+ <field name="long_name">TYRO protein tyrosine kinase binding protein</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+Nasu-Hakola disease [MIM:221770]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TYRP1">
+ <field name="name">TYRP1</field>
+ <field name="long_name">tyrosinase-related protein 1</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p23</field>
+ <field name="info">
+Albinism, brown [MIM:203290]
+Albinism, rufous [MIM:278400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TYR">
+ <field name="name">TYR</field>
+ <field name="long_name">tyrosinase (oculocutaneous albinism IA)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q14-q21</field>
+ <field name="info">
+Albinism, oculocutaneous, type IA [MIM:203100]
+Waardenburg syndrome/albinism, digenic [MIM:103470]
+Albinism, oculocutaneous, type IB [MIM:606952]
+Skin/hair/eye pigmentation 3, freckling [MIM:601800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="TYS">
+ <field name="name">TYS</field>
+ <field name="long_name">sclerotylosis</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q23</field>
+ <field name="info">
+Huriez syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="T">
+ <field name="name">T</field>
+ <field name="long_name">T, brachyury homolog (mouse)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q27</field>
+ <field name="info">
+Neural tube defects, susceptibility to [MIM:182940]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UAQTL3">
+ <field name="name">UAQTL3</field>
+ <field name="long_name">Uric acid concentration, serum, QTL3</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q22</field>
+ <field name="info">
+Uric acid concentration, serum, QTL3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UAQTL4">
+ <field name="name">UAQTL4</field>
+ <field name="long_name">Uric acid concentration, serum, QTL4</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21</field>
+ <field name="info">
+Uric acid concentration, serum, QTL4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UBB">
+ <field name="name">UBB</field>
+ <field name="long_name">ubiquitin B</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p12-p11.1</field>
+ <field name="info">
+Cleft palate, isolated [MIM:119540]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UBE2A">
+ <field name="name">UBE2A</field>
+ <field name="long_name">ubiquitin-conjugating enzyme E2A (RAD6 homolog)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24-q25</field>
+ <field name="info">
+Mental retardation, X-linked syndromic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UBE2B">
+ <field name="name">UBE2B</field>
+ <field name="long_name">ubiquitin-conjugating enzyme E2B (RAD6 homolog)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q23-q31</field>
+ <field name="info">
+Male infertility</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UBE3A">
+ <field name="name">UBE3A</field>
+ <field name="long_name">ubiquitin protein ligase E3A</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q11-q13</field>
+ <field name="info">
+Angelman syndrome [MIM:105830]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UBIAD1">
+ <field name="name">UBIAD1</field>
+ <field name="long_name">UbiA prenyltransferase domain containing 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p36.3</field>
+ <field name="info">
+Corneal dystrophy, crystalline, of Schnyder [MIM:121800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UBM2">
+ <field name="name">UBM2</field>
+ <field name="long_name">Melanoma, uveal, susceptibility to, 2</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25.2-p25.1</field>
+ <field name="info">
+Melanoma, uveal, susceptibility to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UBR1">
+ <field name="name">UBR1</field>
+ <field name="long_name">ubiquitin protein ligase E3 component n-recognin 1</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q15-q21.1</field>
+ <field name="info">
+Johanson-Blizzard syndrome [MIM:243800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UCHL1">
+ <field name="name">UCHL1</field>
+ <field name="long_name">ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p14</field>
+ <field name="info">
+Parkinson disease, familial [MIM:168600]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UCP1">
+ <field name="name">UCP1</field>
+ <field name="long_name">uncoupling protein 1 (mitochondrial, proton carrier)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q31</field>
+ <field name="info">
+Obesity, susceptibility to [MIM:601665]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UCP2">
+ <field name="name">UCP2</field>
+ <field name="long_name">uncoupling protein 2 (mitochondrial, proton carrier)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Obesity, susceptibility to, BMIQ4 [MIM:607447]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UCP3">
+ <field name="name">UCP3</field>
+ <field name="long_name">uncoupling protein 3 (mitochondrial, proton carrier)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Obesity, severe, and type II diabetes [MIM:601665]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UFD1L">
+ <field name="name">UFD1L</field>
+ <field name="long_name">ubiquitin fusion degradation 1 like (yeast)</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UFS">
+ <field name="name">UFS</field>
+ <field name="long_name">urofacial syndrome</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q23-q24</field>
+ <field name="info">
+Urofacial syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UGT1A10">
+ <field name="name">UGT1A10</field>
+ <field name="long_name">UDP glucuronosyltransferase 1 family, polypeptide A10</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UGT1A1">
+ <field name="name">UGT1A1</field>
+ <field name="long_name">UDP glucuronosyltransferase 1 family, polypeptide A1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37</field>
+ <field name="info">
+Crigler-Najjar syndrome, type I [MIM:218800]
+Gilbert syndrome [MIM:143500]
+Crigler-Najjar syndrome, type II [MIM:606785]
+Hyperbilirubinemia, familial transcient neonatal [MIM:237900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UGT1A3">
+ <field name="name">UGT1A3</field>
+ <field name="long_name">UDP glucuronosyltransferase 1 family, polypeptide A3</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UGT1A4">
+ <field name="name">UGT1A4</field>
+ <field name="long_name">UDP glucuronosyltransferase 1 family, polypeptide A4</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UGT1A6">
+ <field name="name">UGT1A6</field>
+ <field name="long_name">UDP glucuronosyltransferase 1 family, polypeptide A6</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UGT1A7">
+ <field name="name">UGT1A7</field>
+ <field name="long_name">UDP glucuronosyltransferase 1 family, polypeptide A7</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UGT1A8">
+ <field name="name">UGT1A8</field>
+ <field name="long_name">UDP glucuronosyltransferase 1 family, polypeptide A8</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UGT1A9">
+ <field name="name">UGT1A9</field>
+ <field name="long_name">UDP glucuronosyltransferase 1 family, polypeptide A9</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q37</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UGT2B15">
+ <field name="name">UGT2B15</field>
+ <field name="long_name">UDP glucuronosyltransferase 2 family, polypeptide B15</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UGT2B17">
+ <field name="name">UGT2B17</field>
+ <field name="long_name">UDP glucuronosyltransferase 2 family, polypeptide B17</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UGT2B7">
+ <field name="name">UGT2B7</field>
+ <field name="long_name">UDP glucuronosyltransferase 2 family, polypeptide B7</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UMOD">
+ <field name="name">UMOD</field>
+ <field name="long_name">uromodulin</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p12.3</field>
+ <field name="info">
+Hyperuricemic nephropathy, familial juvenile [MIM:162000]
+Medullary cystic kidney disease 2 [MIM:603860]
+Glomerulocystic kidney disease with hyperuricemia and isosthenuria [MIM:609886]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UMPS">
+ <field name="name">UMPS</field>
+ <field name="long_name">uridine monophosphate synthetase</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q13</field>
+ <field name="info">
+Oroticaciduria</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UNC119">
+ <field name="name">UNC119</field>
+ <field name="long_name">unc-119 homolog (C. elegans)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q11.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UNC13D">
+ <field name="name">UNC13D</field>
+ <field name="long_name">unc-13 homolog D (C. elegans)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25.1</field>
+ <field name="info">
+Hemophagocytic lymphohistiocytosis, familial, 3 [MIM:608898]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UNC93A">
+ <field name="name">UNC93A</field>
+ <field name="long_name">unc-93 homolog A (C. elegans)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q27</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UNC93B1">
+ <field name="name">UNC93B1</field>
+ <field name="long_name">unc-93 homolog B1 (C. elegans)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Herpes simplex encephalitis, UNC93B-deficient [MIM:610551]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UNG">
+ <field name="name">UNG</field>
+ <field name="long_name">uracil-DNA glycosylase</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q23-q24.1</field>
+ <field name="info">
+Immunodeficiency with hyper IgM, type 4 [MIM:608106]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UOX">
+ <field name="name">UOX</field>
+ <field name="long_name">urate oxidase (pseudogene)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p22</field>
+ <field name="info">
+Urate oxidase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UPB1">
+ <field name="name">UPB1</field>
+ <field name="long_name">ureidopropionase, beta</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.2</field>
+ <field name="info">
+Beta-ureidopropionase deficiency</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UPF3B">
+ <field name="name">UPF3B</field>
+ <field name="long_name">UPF3 regulator of nonsense transcripts homolog B (yeast)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq25-q26</field>
+ <field name="info">
+Mental retardation, X-linked, syndromic 14 [MIM:300676]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UPK3A">
+ <field name="name">UPK3A</field>
+ <field name="long_name">uroplakin 3A</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q13.31</field>
+ <field name="info">
+Renal adysplasia [MIM:191830]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UQCRB">
+ <field name="name">UQCRB</field>
+ <field name="long_name">ubiquinol-cytochrome c reductase binding protein</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q22</field>
+ <field name="info">
+Mitochondrial complex III deficiency [MIM:124000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UQCRQ">
+ <field name="name">UQCRQ</field>
+ <field name="long_name">ubiquinol-cytochrome c reductase, complex III subunit VII, 9.5kDa</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q31.1</field>
+ <field name="info">
+Mitochondrial complex III deficiency [MIM:124000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UROD">
+ <field name="name">UROD</field>
+ <field name="long_name">uroporphyrinogen decarboxylase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34</field>
+ <field name="info">
+Porphyria cutanea tarda
+Porphyria, hepatoerythropoietic</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UROS">
+ <field name="name">UROS</field>
+ <field name="long_name">uroporphyrinogen III synthase</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q25.2-q26.3</field>
+ <field name="info">
+Porphyria, congenital erythropoietic [MIM:263700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="USF1">
+ <field name="name">USF1</field>
+ <field name="long_name">upstream transcription factor 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q22-q23</field>
+ <field name="info">
+Hyperlipidemia, familial combined, susceptibility to [MIM:602491]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="USH1C">
+ <field name="name">USH1C</field>
+ <field name="long_name">Usher syndrome 1C (autosomal recessive, severe)</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.1</field>
+ <field name="info">
+Usher syndrome, type 1C [MIM:276904]
+Deafness, autosomal recessive 18 [MIM:602092]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="USH1E">
+ <field name="name">USH1E</field>
+ <field name="long_name">Usher syndrome 1E (autosomal recessive, severe)</field>
+ <field name="chromosome">21</field>
+ <field name="location">21q21</field>
+ <field name="info">
+Usher syndrome, type 1E</field>
+</record>
+<record model="gnuhealth.disease.gene" id="USH1G">
+ <field name="name">USH1G</field>
+ <field name="long_name">Usher syndrome 1G (autosomal recessive)</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q24-q25</field>
+ <field name="info">
+Usher syndrome, type 1G [MIM:606943]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="USH1H">
+ <field name="name">USH1H</field>
+ <field name="long_name">Usher syndrome 1H (autosomal recessive)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q22-q23</field>
+ <field name="info">
+Usher syndrome, type 1H</field>
+</record>
+<record model="gnuhealth.disease.gene" id="USH2A">
+ <field name="name">USH2A</field>
+ <field name="long_name">Usher syndrome 2A (autosomal recessive, mild)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q41</field>
+ <field name="info">
+Usher syndrome, type 2A [MIM:276901]
+Retinitis pigmentosa-39 [MIM:268000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="USH2B">
+ <field name="name">USH2B</field>
+ <field name="long_name">Usher syndrome 2B (autosomal recessive, mild)</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q14</field>
+ <field name="info">
+Convulsions, familial febrile, 4 [MIM:604352]
+Usher syndrome, type IIC [MIM:605472]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="USP24">
+ <field name="name">USP24</field>
+ <field name="long_name">ubiquitin specific peptidase 24</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="USP26">
+ <field name="name">USP26</field>
+ <field name="long_name">ubiquitin specific peptidase 26</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="USP9Y">
+ <field name="name">USP9Y</field>
+ <field name="long_name">ubiquitin specific peptidase 9, Y-linked</field>
+ <field name="chromosome">Y</field>
+ <field name="location">Yq11.2</field>
+ <field name="info">
+Azoospermia [MIM:415000]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="UST">
+ <field name="name">UST</field>
+ <field name="long_name">uronyl-2-sulfotransferase</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q25.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="UVM1">
+ <field name="name">UVM1</field>
+ <field name="long_name">Melanoma, uveal, susceptibility to, 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q24-q26</field>
+ <field name="info">
+Melanoma, uveal, susceptibility to, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VANGL1">
+ <field name="name">VANGL1</field>
+ <field name="long_name">vang-like 1 (van gogh, Drosophila)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13</field>
+ <field name="info">
+Caudal regression syndrome [MIM:600145]
+Neural tube defects [MIM:182940]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VAPB">
+ <field name="name">VAPB</field>
+ <field name="long_name">VAMP (vesicle-associated membrane protein)-associated protein B and C</field>
+ <field name="chromosome">20</field>
+ <field name="location">20q13.3</field>
+ <field name="info">
+Amyotrophic lateral sclerosis 8 [MIM:608627]
+Spinal muscular atrophy, late-onset, Finkel type [MIM:182980]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VAX1">
+ <field name="name">VAX1</field>
+ <field name="long_name">ventral anterior homeobox 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q26.1</field>
+ <field name="info">
+Anophthalmia/Microphthalmia</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VCAM1">
+ <field name="name">VCAM1</field>
+ <field name="long_name">vascular cell adhesion molecule 1</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p32-p31</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="VCL">
+ <field name="name">VCL</field>
+ <field name="long_name">vinculin</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q22.1-q23</field>
+ <field name="info">
+Cardiomyopathy, dilated, 1W [MIM:611407]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VCP">
+ <field name="name">VCP</field>
+ <field name="long_name">valosin-containing protein</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p13-p12</field>
+ <field name="info">
+Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia [MIM:167320]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VCX3A">
+ <field name="name">VCX3A</field>
+ <field name="long_name">variable charge, X-linked 3A</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="VDR">
+ <field name="name">VDR</field>
+ <field name="long_name">vitamin D (1,25- dihydroxyvitamin D3) receptor</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q12-q14</field>
+ <field name="info">
+Rickets, vitamin D-resistant, type IIA [MIM:277440]
+Osteoporosis, involutional [MIM:166710]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VHL">
+ <field name="name">VHL</field>
+ <field name="long_name">von Hippel-Lindau tumor suppressor</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p26-p25</field>
+ <field name="info">
+von Hippel-Lindau syndrome [MIM:193300]
+Renal cell carcinoma, somatic [MIM:144700]
+Pheochromocytoma [MIM:171300]
+Hemangioblastoma, cerebellar, somatic
+Polycythemia, benign familial [MIM:263400]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VIL1">
+ <field name="name">VIL1</field>
+ <field name="long_name">villin 1</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35-q36</field>
+ <field name="info">
+Cholestasis, progressive canalicular</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VKORC1">
+ <field name="name">VKORC1</field>
+ <field name="long_name">vitamin K epoxide reductase complex, subunit 1</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p11.2</field>
+ <field name="info">
+Vitamin K-dependent clotting factors, combined deficiency of, 2 [MIM:607473]
+Warfarin resistance [MIM:122700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VLDLR">
+ <field name="name">VLDLR</field>
+ <field name="long_name">very low density lipoprotein receptor</field>
+ <field name="chromosome">9</field>
+ <field name="location">9p24</field>
+ <field name="info">
+Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion [MIM:224050]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VMD1">
+ <field name="name">VMD1</field>
+ <field name="long_name">vitelliform macular dystrophy, atypical</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q24</field>
+ <field name="info">
+Macular dystrophy, atypical vitelliform</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VNN1">
+ <field name="name">VNN1</field>
+ <field name="long_name">vanin 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q23-q24</field>
+ <field name="info">
+High density lipoprotein cholesterol level QTL 8</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VPS13A">
+ <field name="name">VPS13A</field>
+ <field name="long_name">vacuolar protein sorting 13 homolog A (S. cerevisiae)</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q21</field>
+ <field name="info">
+Choreoacanthocytosis [MIM:200150]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VPS33B">
+ <field name="name">VPS33B</field>
+ <field name="long_name">vacuolar protein sorting 33 homolog B (yeast)</field>
+ <field name="chromosome">15</field>
+ <field name="location">15q26.1</field>
+ <field name="info">
+ARC syndrome [MIM:208085]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VRNI">
+ <field name="name">VRNI</field>
+ <field name="long_name">vitreoretinopathy, neovascular inflammatory</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q13</field>
+ <field name="info">
+Vitreoretinopathy, neovascular inflammatory</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VSPA">
+ <field name="name">VSPA</field>
+ <field name="long_name">Visuospatial/perceptual abilities</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.33</field>
+ <field name="info">
+Turner syndrome-associated neurocognitive phenotype
+Visuospatial/perceptual abilities</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VSX1">
+ <field name="name">VSX1</field>
+ <field name="long_name">visual system homeobox 1</field>
+ <field name="chromosome">20</field>
+ <field name="location">20p11.2</field>
+ <field name="info">
+Keratoconus [MIM:148300]
+Corneal dystrophy, hereditary polymorphous posterior [MIM:122000]
+Craniofacial anomalies, empty sella turcica, corneal endothelial changes, and abnormal retinal and auditory bipolar cells</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VTLG">
+ <field name="name">VTLG</field>
+ <field name="long_name">Vitiligo</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Vitiligo, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VUR">
+ <field name="name">VUR</field>
+ <field name="long_name">Vesicoureteral reflux</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p13</field>
+ <field name="info">
+Vesicoureteral reflux</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VWF">
+ <field name="name">VWF</field>
+ <field name="long_name">von Willebrand factor</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.3</field>
+ <field name="info">
+von Willebrand disease, autosomal dominant
+von Willebrand disease, autosomal recessive [MIM:277480]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VWS2">
+ <field name="name">VWS2</field>
+ <field name="long_name">van der Woude syndrome 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34</field>
+ <field name="info">
+van der Woude syndrome 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="VWS">
+ <field name="name">VWS</field>
+ <field name="long_name">Van der Woude syndrome</field>
+ <field name="chromosome">1</field>
+ <field name="location">1q32-q41</field>
+ <field name="info">
+van der Woude syndrome [MIM:119300]
+Popliteal pterygium syndrome [MIM:119500]
+Orofacial cleft 6 [MIM:608864]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WAGRO">
+ <field name="name">WAGRO</field>
+ <field name="long_name">WAGRO syndrome</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13-p12</field>
+ <field name="info">
+WAGRO syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WAS">
+ <field name="name">WAS</field>
+ <field name="long_name">Wiskott-Aldrich syndrome (eczema-thrombocytopenia)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11.23-p11.22</field>
+ <field name="info">
+Wiskott-Aldrich syndrome [MIM:301000]
+Thrombocytopenia, X-linked [MIM:313900]
+Neutropenia, severe congenital, X-linked [MIM:300299]
+Thrombocytopenia, X-linked, intermittent [MIM:313900]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WDM">
+ <field name="name">WDM</field>
+ <field name="long_name">Welander distal myopathy</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p13</field>
+ <field name="info">
+Welander distal myopathy</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WDR36">
+ <field name="name">WDR36</field>
+ <field name="long_name">WD repeat domain 36</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q21.3-q22.1</field>
+ <field name="info">
+Glaucoma 1, open angle, G [MIM:609887]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WFS1">
+ <field name="name">WFS1</field>
+ <field name="long_name">Wolfram syndrome 1 (wolframin)</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.1</field>
+ <field name="info">
+Wolfram syndrome [MIM:222300]
+Hearing loss, low-frequency sensorineural [MIM:600965]
+Wolfram-like syndrome, autosomal dominant [MIM:222300]
+Diabetes mellitus, noninsulin-dependent, association with [MIM:125853]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WG">
+ <field name="name">WG</field>
+ <field name="long_name">Wegener granulomatosis</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Wegener granulomatosis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WHSC1L1">
+ <field name="name">WHSC1L1</field>
+ <field name="long_name">Wolf-Hirschhorn syndrome candidate 1-like 1</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p12</field>
+ <field name="info">
+Leukemia, acute myeloid [MIM:601626]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WHSC1">
+ <field name="name">WHSC1</field>
+ <field name="long_name">Wolf-Hirschhorn syndrome candidate 1</field>
+ <field name="chromosome">4</field>
+ <field name="location">4p16.3</field>
+ <field name="info">
+Wolf-Hirschhorn syndrome [MIM:194190]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WISP3">
+ <field name="name">WISP3</field>
+ <field name="long_name">WNT1 inducible signaling pathway protein 3</field>
+ <field name="chromosome">6</field>
+ <field name="location">6q22-q23</field>
+ <field name="info">
+Arthropathy, progressive pseudorheumatoid, of childhood [MIM:208230]
+Spondyloepiphyseal dysplasia tarda with progressive arthropathy [MIM:208230]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WM1">
+ <field name="name">WM1</field>
+ <field name="long_name">Macroglobulinemia, Waldenstrom, susceptibility to, 1</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p21.3</field>
+ <field name="info">
+Macroglobulinemia, Waldenstrom, susceptibility to, 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WM2">
+ <field name="name">WM2</field>
+ <field name="long_name">Macroglobulinemia, Waldenstrom, susceptibility to, 2</field>
+ <field name="chromosome">4</field>
+ <field name="location">4q</field>
+ <field name="info">
+Macroglobulinemia, Waldenstrom, susceptibility to, 2</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WNK1">
+ <field name="name">WNK1</field>
+ <field name="long_name">WNK lysine deficient protein kinase 1</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13</field>
+ <field name="info">
+Pseudohypoaldosteronism, type IIC [MIM:145260]
+Neuropathy, hereditary sensory and autonomic, type II [MIM:201300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WNK4">
+ <field name="name">WNK4</field>
+ <field name="long_name">WNK lysine deficient protein kinase 4</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21-q22</field>
+ <field name="info">
+Pseudohypoaldosteronism type II [MIM:145260]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WNT10A">
+ <field name="name">WNT10A</field>
+ <field name="long_name">wingless-type MMTV integration site family, member 10A</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35</field>
+ <field name="info">
+Odontoonychodermal dysplasia [MIM:257980]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WNT10B">
+ <field name="name">WNT10B</field>
+ <field name="long_name">wingless-type MMTV integration site family, member 10B</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="WNT3">
+ <field name="name">WNT3</field>
+ <field name="long_name">wingless-type MMTV integration site family, member 3</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21</field>
+ <field name="info">
+Tetra-amelia, autosomal recessive [MIM:273395]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WNT4">
+ <field name="name">WNT4</field>
+ <field name="long_name">wingless-type MMTV integration site family, member 4</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p35</field>
+ <field name="info">
+SERKAL syndrome [MIM:611812]
+Mullerian aplasia and hyperandrogenism [MIM:158330]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WNT5B">
+ <field name="name">WNT5B</field>
+ <field name="long_name">wingless-type MMTV integration site family, member 5B</field>
+ <field name="chromosome">12</field>
+ <field name="location">12p13.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="WNT7A">
+ <field name="name">WNT7A</field>
+ <field name="long_name">wingless-type MMTV integration site family, member 7A</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25</field>
+ <field name="info">
+Ulna and fibula, absence of, with sever limb deficiency [MIM:276820]
+Fuhrmann syndrome [MIM:228930]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WRN">
+ <field name="name">WRN</field>
+ <field name="long_name">Werner syndrome, RecQ helicase-like</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p12-p11.2</field>
+ <field name="info">
+Werner syndrome [MIM:277700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WS2A">
+ <field name="name">WS2A</field>
+ <field name="long_name">Waardenburg syndrome, type 2A</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p14.1-p12.3</field>
+ <field name="info">
+Waardenburg syndrome, type IIA [MIM:193510]
+Waardenburg syndrome/ocular albinism, digenic [MIM:103470]
+Tietz syndrome [MIM:103500]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WS2B">
+ <field name="name">WS2B</field>
+ <field name="long_name">Waardenburg syndrome, type 2B</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p21-p13.3</field>
+ <field name="info">
+Waardenburg syndrome, type 2B</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WS2C">
+ <field name="name">WS2C</field>
+ <field name="long_name">Waardenburg syndrome, type IIC</field>
+ <field name="chromosome">8</field>
+ <field name="location">8p23</field>
+ <field name="info">
+Waardenburg syndrome, type IIC</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WSN">
+ <field name="name">WSN</field>
+ <field name="long_name">Waisman syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq28</field>
+ <field name="info">
+Waisman parkinsonism-mental retardation syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WT1">
+ <field name="name">WT1</field>
+ <field name="long_name">Wilms tumor 1</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p13</field>
+ <field name="info">
+Wilms tumor, type 1 [MIM:194070]
+Denys-Drash syndrome [MIM:194080]
+Mesangial sclerosis, isolated diffuse [MIM:256370]
+WAGR syndrome [MIM:194072]
+Frasier syndrome [MIM:136680]
+Meacham syndrome [MIM:608978]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WT2">
+ <field name="name">WT2</field>
+ <field name="long_name">Wilms tumor 2</field>
+ <field name="chromosome">11</field>
+ <field name="location">11p15.5</field>
+ <field name="info">
+Wilms tumor, type 2
+Adrenocortical carcinoma, hereditary [MIM:202300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WT3">
+ <field name="name">WT3</field>
+ <field name="long_name">Wilms tumor-3</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q</field>
+ <field name="info">
+Wilms tumor, type 3</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WT4">
+ <field name="name">WT4</field>
+ <field name="long_name">Wilms tumor-4</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q12-q21</field>
+ <field name="info">
+Wilms tumor, type 4</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WTS">
+ <field name="name">WTS</field>
+ <field name="long_name">Wilson-Turner X-linked mental retardation syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp21.1-q22</field>
+ <field name="info">
+Mental retardation, X-linked, syndromic-6, with gynecomastia and obesity</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WWC1">
+ <field name="name">WWC1</field>
+ <field name="long_name">WW and C2 domain containing 1</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q34-q35.2</field>
+ <field name="info">
+Memory, enhanced, association with</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WWOX">
+ <field name="name">WWOX</field>
+ <field name="long_name">WW domain containing oxidoreductase</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q23.3-q24.1</field>
+ <field name="info">
+Esophageal squamous cell carcinoma [MIM:133239]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="WWS">
+ <field name="name">WWS</field>
+ <field name="long_name">Wieacker-Wolff syndrome</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13-q21</field>
+ <field name="info">
+Wieacker-Wolff syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XBP1">
+ <field name="name">XBP1</field>
+ <field name="long_name">X-box binding protein 1</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q12</field>
+ <field name="info">
+Major affective disorder-7, susceptibility to [MIM:612371]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XCE">
+ <field name="name">XCE</field>
+ <field name="long_name">X chromosome controlling element</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.2</field>
+ <field name="info">
+X-inactivation, familial skewed [MIM:300087]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XDH">
+ <field name="name">XDH</field>
+ <field name="long_name">xanthine dehydrogenase</field>
+ <field name="chromosome">2</field>
+ <field name="location">2p23-p22</field>
+ <field name="info">
+Xanthinuria, type I [MIM:278300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XGPY">
+ <field name="name">XGPY</field>
+ <field name="long_name">Xg pseudogene, Y-linked</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xpter-p22.32</field>
+ <field name="info">
+Blood group, XG system</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XG">
+ <field name="name">XG</field>
+ <field name="long_name">Xg blood group</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xpter-p22.32</field>
+ <field name="info">
+Blood group, XG system</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XIAP">
+ <field name="name">XIAP</field>
+ <field name="long_name">X-linked inhibitor of apoptosis</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq25</field>
+ <field name="info">
+Lymphoproliferative syndrome, X-linked, 2 [MIM:300635]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XIC">
+ <field name="name">XIC</field>
+ <field name="long_name">X chromosome inactivation center</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.2</field>
+ <field name="info">
+X-inactivation, familial skewed [MIM:300087]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XIST">
+ <field name="name">XIST</field>
+ <field name="long_name">X (inactive)-specific transcript (non-protein coding)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.2</field>
+ <field name="info">
+X-inactivation, familial skewed [MIM:300087]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XK">
+ <field name="name">XK</field>
+ <field name="long_name">X-linked Kx blood group (McLeod syndrome)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp21.2-p21.1</field>
+ <field name="info">
+McLeod syndrome
+McLeod syndrome with neuroacanthosis</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XPA">
+ <field name="name">XPA</field>
+ <field name="long_name">xeroderma pigmentosum, complementation group A</field>
+ <field name="chromosome">9</field>
+ <field name="location">9q22.3</field>
+ <field name="info">
+Xeroderma pigmentosum, group A [MIM:278700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XPC">
+ <field name="name">XPC</field>
+ <field name="long_name">xeroderma pigmentosum, complementation group C</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p25</field>
+ <field name="info">
+Xeroderma pigmentosum, group C</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XPNPEP2">
+ <field name="name">XPNPEP2</field>
+ <field name="long_name">X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq25</field>
+ <field name="info">
+Angioedema induced by ACE inhibitors, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XRCC1">
+ <field name="name">XRCC1</field>
+ <field name="long_name">X-ray repair complementing defective repair in Chinese hamster cells 1</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="XRCC2">
+ <field name="name">XRCC2</field>
+ <field name="long_name">X-ray repair complementing defective repair in Chinese hamster cells 2</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q36.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="XRCC3">
+ <field name="name">XRCC3</field>
+ <field name="long_name">X-ray repair complementing defective repair in Chinese hamster cells 3</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q32.3</field>
+ <field name="info">
+Melanoma, cutaneous malignant, susceptibility to
+Breast cancer, susceptibility to</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XRCC4">
+ <field name="name">XRCC4</field>
+ <field name="long_name">X-ray repair complementing defective repair in Chinese hamster cells 4</field>
+ <field name="chromosome">5</field>
+ <field name="location">5q13-q14</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="XRCC5">
+ <field name="name">XRCC5</field>
+ <field name="long_name">X-ray repair complementing defective repair in Chinese hamster cells 5 (double-strand-break rejoining)</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q35</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="XYLT1">
+ <field name="name">XYLT1</field>
+ <field name="long_name">xylosyltransferase I</field>
+ <field name="chromosome">16</field>
+ <field name="location">16p13.1</field>
+ <field name="info">
+Pseudoxanthoma elasticum, modifier of severity of [MIM:264800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="XYLT2">
+ <field name="name">XYLT2</field>
+ <field name="long_name">xylosyltransferase II</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q21.3-q22</field>
+ <field name="info">
+Pseudoxanthoma elasticum, modifier of severity of [MIM:264800]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="YARS">
+ <field name="name">YARS</field>
+ <field name="long_name">tyrosyl-tRNA synthetase</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p35</field>
+ <field name="info">
+Charcot-Marie-Tooth disease, dominant intermediate C [MIM:608323]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="YEATS4">
+ <field name="name">YEATS4</field>
+ <field name="long_name">YEATS domain containing 4</field>
+ <field name="chromosome">12</field>
+ <field name="location">12q13-q15</field>
+ <field name="info">
+Glioma</field>
+</record>
+<record model="gnuhealth.disease.gene" id="YTHDF2">
+ <field name="name">YTHDF2</field>
+ <field name="long_name">YTH domain family, member 2</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p35</field>
+ <field name="info">
+Longevity, susceptibility to [MIM:152430]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="YWHAE">
+ <field name="name">YWHAE</field>
+ <field name="long_name">tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide</field>
+ <field name="chromosome">17</field>
+ <field name="location">17p13.3</field>
+ <field name="info">
+Miller-Dieker lissencephaly [MIM:247200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZAP70">
+ <field name="name">ZAP70</field>
+ <field name="long_name">zeta-chain (TCR) associated protein kinase 70kDa</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q12</field>
+ <field name="info">
+Selective T-cell defect</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZBTB16">
+ <field name="name">ZBTB16</field>
+ <field name="long_name">zinc finger and BTB domain containing 16</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.1</field>
+ <field name="info">
+Leukemia, acute promyelocytic, PL2F/RARA type
+Skeletal defects, genital hypoplasia, and mental retardation [MIM:612447]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZCCHC12">
+ <field name="name">ZCCHC12</field>
+ <field name="long_name">zinc finger, CCHC domain containing 12</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZD1">
+ <field name="name">ZD1</field>
+ <field name="long_name">Zygodactyly 1</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p21.31</field>
+ <field name="info">
+Zygodactyly 1</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZDHHC15">
+ <field name="name">ZDHHC15</field>
+ <field name="long_name">zinc finger, DHHC-type containing 15</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq13.3</field>
+ <field name="info">
+Mental retardation, X-linked-91 [MIM:300577]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZDHHC8">
+ <field name="name">ZDHHC8</field>
+ <field name="long_name">zinc finger, DHHC-type containing 8</field>
+ <field name="chromosome">22</field>
+ <field name="location">22q11.21</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZDHHC9">
+ <field name="name">ZDHHC9</field>
+ <field name="long_name">zinc finger, DHHC-type containing 9</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26.1</field>
+ <field name="info">
+Mental retardation, X-linked, ZDHHC9-related</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZEB1">
+ <field name="name">ZEB1</field>
+ <field name="long_name">zinc finger E-box binding homeobox 1</field>
+ <field name="chromosome">10</field>
+ <field name="location">10p11.2</field>
+ <field name="info">
+Corneal dystrophy, posterior polymorphous, 3 [MIM:609141]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZEB2">
+ <field name="name">ZEB2</field>
+ <field name="long_name">zinc finger E-box binding homeobox 2</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q22</field>
+ <field name="info">
+Mowat-Wilson syndrome [MIM:235730]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZFHX3">
+ <field name="name">ZFHX3</field>
+ <field name="long_name">zinc finger homeobox 3</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q22.3-q23.1</field>
+ <field name="info">
+Prostate cancer, susceptibility to [MIM:176807]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZFHX4">
+ <field name="name">ZFHX4</field>
+ <field name="long_name">zinc finger homeobox 4</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q21.12</field>
+ <field name="info">
+Ptosis, congenital [MIM:178300]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZFP36L1">
+ <field name="name">ZFP36L1</field>
+ <field name="long_name">zinc finger protein 36, C3H type-like 1</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q22-q24</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZFP36">
+ <field name="name">ZFP36</field>
+ <field name="long_name">zinc finger protein 36, C3H type, homolog (mouse)</field>
+ <field name="chromosome">19</field>
+ <field name="location">19q13.1</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZFP57">
+ <field name="name">ZFP57</field>
+ <field name="long_name">zinc finger protein 57 homolog (mouse)</field>
+ <field name="chromosome">6</field>
+ <field name="location">6p22.1</field>
+ <field name="info">
+Diabetes mellitus, transient neonatal, 1 [MIM:601410]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZFPM2">
+ <field name="name">ZFPM2</field>
+ <field name="long_name">zinc finger protein, multitype 2</field>
+ <field name="chromosome">8</field>
+ <field name="location">8q23</field>
+ <field name="info">
+Tetralogy of Fallot [MIM:187500]
+Diaphragmatic hernia 3 [MIM:610187]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZFYVE26">
+ <field name="name">ZFYVE26</field>
+ <field name="long_name">zinc finger, FYVE domain containing 26</field>
+ <field name="chromosome">14</field>
+ <field name="location">14q24.1</field>
+ <field name="info">
+Spastic paraplegia 15 [MIM:270700]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZFYVE27">
+ <field name="name">ZFYVE27</field>
+ <field name="long_name">zinc finger, FYVE domain containing 27</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q24.2</field>
+ <field name="info">
+Spastic paraplegia 33 [MIM:610244]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZIC1">
+ <field name="name">ZIC1</field>
+ <field name="long_name">Zic family member 1 (odd-paired homolog, Drosophila)</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q24</field>
+ <field name="info">
+Dandy-Walker malformation [MIM:220200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZIC2">
+ <field name="name">ZIC2</field>
+ <field name="long_name">Zic family member 2 (odd-paired homolog, Drosophila)</field>
+ <field name="chromosome">13</field>
+ <field name="location">13q32</field>
+ <field name="info">
+Holoprosencephaly-5 [MIM:609637]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZIC3">
+ <field name="name">ZIC3</field>
+ <field name="long_name">Zic family member 3 (odd-paired homolog, Drosophila)</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xq26.2</field>
+ <field name="info">
+Heterotaxy, X-linked visceral [MIM:306955]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZIC4">
+ <field name="name">ZIC4</field>
+ <field name="long_name">Zic family member 4</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q24</field>
+ <field name="info">
+Dandy-Walker malformation [MIM:220200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZLS">
+ <field name="name">ZLS</field>
+ <field name="long_name">Zimmerman-Laband Syndrome</field>
+ <field name="chromosome">3</field>
+ <field name="location">3p14.3</field>
+ <field name="info">
+Zimmermann-Laband syndrome</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZMPSTE24">
+ <field name="name">ZMPSTE24</field>
+ <field name="long_name">zinc metallopeptidase (STE24 homolog, S. cerevisiae)</field>
+ <field name="chromosome">1</field>
+ <field name="location">1p34</field>
+ <field name="info">
+Mandibuloacral dysplasia with type B lipodystrophy [MIM:608612]
+Restrictive dermopathy, lethal [MIM:275210]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZNF148">
+ <field name="name">ZNF148</field>
+ <field name="long_name">zinc finger protein 148</field>
+ <field name="chromosome">3</field>
+ <field name="location">3q21</field>
+ <field name="info">
+Sertoli-cell-only syndrome [MIM:400042]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZNF202">
+ <field name="name">ZNF202</field>
+ <field name="long_name">zinc finger protein 202</field>
+ <field name="chromosome">11</field>
+ <field name="location">11q23.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZNF24">
+ <field name="name">ZNF24</field>
+ <field name="long_name">zinc finger protein 24</field>
+ <field name="chromosome">18</field>
+ <field name="location">18q12</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZNF365">
+ <field name="name">ZNF365</field>
+ <field name="long_name">zinc finger protein 365</field>
+ <field name="chromosome">10</field>
+ <field name="location">10q21.2</field>
+ <field name="info">
+Nephrolithiasis, uric acid, susceptibility to [MIM:605990]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZNF385B">
+ <field name="name">ZNF385B</field>
+ <field name="long_name">zinc finger protein 385B</field>
+ <field name="chromosome">2</field>
+ <field name="location">2q31.2-q31.3</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZNF41">
+ <field name="name">ZNF41</field>
+ <field name="long_name">zinc finger protein 41</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.1-cen</field>
+ <field name="info">
+Mental retardation, X-linked-89</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZNF469">
+ <field name="name">ZNF469</field>
+ <field name="long_name">zinc finger protein 469</field>
+ <field name="chromosome">16</field>
+ <field name="location">16q24</field>
+ <field name="info">
+Brittle cornea syndrome [MIM:229200]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZNF627">
+ <field name="name">ZNF627</field>
+ <field name="long_name">zinc finger protein 627</field>
+ <field name="chromosome">19</field>
+ <field name="location">19p13.2</field>
+ <field name="info">
+mutations </field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZNF674">
+ <field name="name">ZNF674</field>
+ <field name="long_name">zinc finger family member 674</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp11</field>
+ <field name="info">
+Mental retardation, X-linked-92</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZNF750">
+ <field name="name">ZNF750</field>
+ <field name="long_name">zinc finger protein 750</field>
+ <field name="chromosome">17</field>
+ <field name="location">17q25.3</field>
+ <field name="info">
+Seborrhea-like dermatitis with psoriasiform elements [MIM:610227]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZNF81">
+ <field name="name">ZNF81</field>
+ <field name="long_name">zinc finger protein 81</field>
+ <field name="chromosome">X</field>
+ <field name="location">Xp22.1-p11</field>
+ <field name="info">
+Mental retardation, X-linked 45 [MIM:300498]</field>
+</record>
+<record model="gnuhealth.disease.gene" id="ZWS1">
+ <field name="name">ZWS1</field>
+ <field name="long_name">Zellweger syndrome 1</field>
+ <field name="chromosome">7</field>
+ <field name="location">7q21-q22</field>
+ <field name="info">
+Zellweger syndrome-1 [MIM:214100]
+Adrenoleukodystrophy, neonatal [MIM:202370]
+Refsum disease, infantile [MIM:266510]</field>
+</record>
+</data>
+</tryton>
diff --git a/debian/changelog b/debian/changelog
new file mode 100644
index 0000000..b4ff969
--- /dev/null
+++ b/debian/changelog
@@ -0,0 +1,5 @@
+tryton-modules-health-genetics (2.8.1-1) unstable; urgency=medium
+
+ * Initial packaging.
+
+ -- Mathias Behrle <mathiasb at m9s.biz> Wed, 18 Feb 2015 10:29:22 +0100
diff --git a/debian/compat b/debian/compat
new file mode 100644
index 0000000..ec63514
--- /dev/null
+++ b/debian/compat
@@ -0,0 +1 @@
+9
diff --git a/debian/control b/debian/control
new file mode 100644
index 0000000..2e6b0b9
--- /dev/null
+++ b/debian/control
@@ -0,0 +1,35 @@
+Source: tryton-modules-health-genetics
+Section: python
+Priority: optional
+Maintainer: Debian Tryton Maintainers <maintainers at debian.tryton.org>
+Uploaders: Mathias Behrle <mathiasb at m9s.biz>
+Build-Depends:
+ debhelper (>= 9),
+ python (>= 2.6.6-3~),
+ python-setuptools,
+ dh-python
+Standards-Version: 3.9.6
+Homepage: http://health.gnu.org/
+Vcs-Browser: http://anonscm.debian.org/gitweb/?p=tryton/tryton-modules-health-genetics.git
+Vcs-Git: git://anonscm.debian.org/tryton/tryton-modules-health-genetics.git
+X-Python-Version: >= 2.7
+
+Package: tryton-modules-health-genetics
+Architecture: all
+Depends:
+ ${misc:Depends},
+ ${python:Depends},
+ python-pkg-resources,
+ tryton-server (>= ${version:tmajor}~),
+ tryton-server (<< ${version:tdev}~),
+ tryton-modules-health (>= ${version:major}~),
+ tryton-modules-health (<< ${version:dev}~),
+Description: Tryton Application Platform (Health Genetics Module)
+ Tryton is a high-level general purpose application platform. It is the base
+ of a complete business solution as well as a comprehensive health and hospital
+ information system (GNUHealth).
+ .
+ This package provides the GNU Health Genetics Module.
+ - Hereditary risks, family history and genetic disorders.
+ - NCBI and GeneCards information, more than 4200 genes associated to
+ diseases.
diff --git a/debian/copyright b/debian/copyright
new file mode 100644
index 0000000..2140016
--- /dev/null
+++ b/debian/copyright
@@ -0,0 +1,381 @@
+Format: http://www.debian.org/doc/packaging-manuals/copyright-format/1.0/
+
+Files: *
+Copyright: 2008-2015 Luis Falcon <lfalcon at gnusolidario.org>
+ 2011-2015 GNU Solidario <health at gnusolidario.org>
+License: GPL-3+
+
+Files: setup.py
+Copyright: 2011 Cédric Krier <ced at b2ck.com>
+License: GPL-3+
+
+Files: icons/*.svg
+Copyright: Leonardo D'Acchille - GNU Solidario
+License: CC-BY-SA-3.0
+
+Files: debian/*
+Copyright: 2015 Mathias Behrle <mathiasb at m9s.biz>
+License: GPL-3+
+
+License: GPL-3+
+ This program is free software: you can redistribute it and/or modify
+ it under the terms of the GNU General Public License as published by
+ the Free Software Foundation, either version 3 of the License, or
+ (at your option) any later version.
+ .
+ This program is distributed in the hope that it will be useful,
+ but WITHOUT ANY WARRANTY; without even the implied warranty of
+ MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the
+ GNU General Public License for more details.
+ .
+ You should have received a copy of the GNU General Public License
+ along with this program. If not, see <http://www.gnu.org/licenses/>.
+ .
+ The complete text of the GNU General Public License
+ can be found in /usr/share/common-licenses/GPL-3 file.
+
+License: CC-BY-SA-3.0
+ Creative Commons Attribution-ShareAlike 3.0 Unported License
+ .
+ THE WORK (AS DEFINED BELOW) IS PROVIDED UNDER THE TERMS OF THIS CREATIVE
+ COMMONS PUBLIC LICENSE ("CCPL" OR "LICENSE"). THE WORK IS PROTECTED BY
+ COPYRIGHT AND/OR OTHER APPLICABLE LAW. ANY USE OF THE WORK OTHER THAN AS
+ AUTHORIZED UNDER THIS LICENSE OR COPYRIGHT LAW IS PROHIBITED.
+ .
+ BY EXERCISING ANY RIGHTS TO THE WORK PROVIDED HERE, YOU ACCEPT AND AGREE
+ TO BE BOUND BY THE TERMS OF THIS LICENSE. TO THE EXTENT THIS LICENSE MAY
+ BE CONSIDERED TO BE A CONTRACT, THE LICENSOR GRANTS YOU THE RIGHTS
+ CONTAINED HERE IN CONSIDERATION OF YOUR ACCEPTANCE OF SUCH TERMS AND
+ CONDITIONS.
+ .
+ 1. Definitions
+ .
+ a. "Adaptation" means a work based upon the Work, or upon the Work and
+ other pre-existing works, such as a translation, adaptation, derivative
+ work, arrangement of music or other alterations of a literary or
+ artistic work, or phonogram or performance and includes cinematographic
+ adaptations or any other form in which the Work may be recast,
+ transformed, or adapted including in any form recognizably derived from
+ the original, except that a work that constitutes a Collection will not
+ be considered an Adaptation for the purpose of this License. For the
+ avoidance of doubt, where the Work is a musical work, performance or
+ phonogram, the synchronization of the Work in timed-relation with a
+ moving image ("synching") will be considered an Adaptation for the
+ purpose of this License.
+ .
+ b. "Collection" means a collection of literary or artistic works, such
+ as encyclopedias and anthologies, or performances, phonograms or
+ broadcasts, or other works or subject matter other than works listed in
+ Section 1(f) below, which, by reason of the selection and arrangement of
+ their contents, constitute intellectual creations, in which the Work is
+ included in its entirety in unmodified form along with one or more other
+ contributions, each constituting separate and independent works in
+ themselves, which together are assembled into a collective whole. A work
+ that constitutes a Collection will not be considered an Adaptation (as
+ defined below) for the purposes of this License.
+ .
+ c. "Creative Commons Compatible License" means a license that is listed
+ at http://creativecommons.org/compatiblelicenses that has been approved
+ by Creative Commons as being essentially equivalent to this License,
+ including, at a minimum, because that license: (i) contains terms that
+ have the same purpose, meaning and effect as the License Elements of
+ this License; and, (ii) explicitly permits the relicensing of
+ adaptations of works made available under that license under this
+ License or a Creative Commons jurisdiction license with the same License
+ Elements as this License.
+ .
+ d. "Distribute" means to make available to the public the original and
+ copies of the Work or Adaptation, as appropriate, through sale or other
+ transfer of ownership.
+ .
+ e. "License Elements" means the following high-level license attributes
+ as selected by Licensor and indicated in the title of this License:
+ Attribution, ShareAlike.
+ .
+ f. "Licensor" means the individual, individuals, entity or entities that
+ offer(s) the Work under the terms of this License.
+ .
+ g. "Original Author" means, in the case of a literary or artistic work,
+ the individual, individuals, entity or entities who created the Work or
+ if no individual or entity can be identified, the publisher; and in
+ addition (i) in the case of a performance the actors, singers,
+ musicians, dancers, and other persons who act, sing, deliver, declaim,
+ play in, interpret or otherwise perform literary or artistic works or
+ expressions of folklore; (ii) in the case of a phonogram the producer
+ being the person or legal entity who first fixes the sounds of a
+ performance or other sounds; and, (iii) in the case of broadcasts, the
+ organization that transmits the broadcast.
+ .
+ h. "Work" means the literary and/or artistic work offered under the
+ terms of this License including without limitation any production in the
+ literary, scientific and artistic domain, whatever may be the mode or
+ form of its expression including digital form, such as a book, pamphlet
+ and other writing; a lecture, address, sermon or other work of the same
+ nature; a dramatic or dramatico-musical work; a choreographic work or
+ entertainment in dumb show; a musical composition with or without words;
+ a cinematographic work to which are assimilated works expressed by a
+ process analogous to cinematography; a work of drawing, painting,
+ architecture, sculpture, engraving or lithography; a photographic work
+ to which are assimilated works expressed by a process analogous to
+ photography; a work of applied art; an illustration, map, plan, sketch
+ or three-dimensional work relative to geography, topography,
+ architecture or science; a performance; a broadcast; a phonogram; a
+ compilation of data to the extent it is protected as a copyrightable
+ work; or a work performed by a variety or circus performer to the extent
+ it is not otherwise considered a literary or artistic work.
+ .
+ i. "You" means an individual or entity exercising rights under this
+ License who has not previously violated the terms of this License with
+ respect to the Work, or who has received express permission from the
+ Licensor to exercise rights under this License despite a previous
+ violation.
+ .
+ j. "Publicly Perform" means to perform public recitations of the Work
+ and to communicate to the public those public recitations, by any means
+ or process, including by wire or wireless means or public digital
+ performances; to make available to the public Works in such a way that
+ members of the public may access these Works from a place and at a place
+ individually chosen by them; to perform the Work to the public by any
+ means or process and the communication to the public of the performances
+ of the Work, including by public digital performance; to broadcast and
+ rebroadcast the Work by any means including signs, sounds or images.
+ .
+ k. "Reproduce" means to make copies of the Work by any means including
+ without limitation by sound or visual recordings and the right of
+ fixation and reproducing fixations of the Work, including storage of a
+ protected performance or phonogram in digital form or other electronic
+ medium.
+ .
+ 2. Fair Dealing Rights. Nothing in this License is intended to reduce,
+ limit, or restrict any uses free from copyright or rights arising from
+ limitations or exceptions that are provided for in connection with the
+ copyright protection under copyright law or other applicable laws.
+ .
+ 3. License Grant. Subject to the terms and conditions of this License,
+ Licensor hereby grants You a worldwide, royalty-free, non-exclusive,
+ perpetual (for the duration of the applicable copyright) license to
+ exercise the rights in the Work as stated below:
+ .
+ a. to Reproduce the Work, to incorporate the Work into one or more
+ Collections, and to Reproduce the Work as incorporated in the
+ Collections;
+ .
+ b. to create and Reproduce Adaptations provided that any such
+ Adaptation, including any translation in any medium, takes reasonable
+ steps to clearly label, demarcate or otherwise identify that changes
+ were made to the original Work. For example, a translation could be
+ marked "The original work was translated from English to Spanish," or a
+ modification could indicate "The original work has been modified.";
+ .
+ c. to Distribute and Publicly Perform the Work including as incorporated
+ in Collections; and,
+ .
+ d. to Distribute and Publicly Perform Adaptations.
+ .
+ e. For the avoidance of doubt:
+ .
+ i. Non-waivable Compulsory License Schemes. In those jurisdictions in
+ which the right to collect royalties through any statutory or compulsory
+ licensing scheme cannot be waived, the Licensor reserves the exclusive
+ right to collect such royalties for any exercise by You of the rights
+ granted under this License;
+ .
+ ii. Waivable Compulsory License Schemes. In those jurisdictions in which
+ the right to collect royalties through any statutory or compulsory
+ licensing scheme can be waived, the Licensor waives the exclusive right
+ to collect such royalties for any exercise by You of the rights granted
+ under this License; and,
+ .
+ iii. Voluntary License Schemes. The Licensor waives the right to collect
+ royalties, whether individually or, in the event that the Licensor is a
+ member of a collecting society that administers voluntary licensing
+ schemes, via that society, from any exercise by You of the rights
+ granted under this License.
+ .
+ The above rights may be exercised in all media and formats whether now
+ known or hereafter devised. The above rights include the right to make
+ such modifications as are technically necessary to exercise the rights
+ in other media and formats. Subject to Section 8(f), all rights not
+ expressly granted by Licensor are hereby reserved.
+ .
+ 4. Restrictions. The license granted in Section 3 above is expressly
+ made subject to and limited by the following restrictions:
+ .
+ a. You may Distribute or Publicly Perform the Work only under the terms
+ of this License. You must include a copy of, or the Uniform Resource
+ Identifier (URI) for, this License with every copy of the Work You
+ Distribute or Publicly Perform. You may not offer or impose any terms on
+ the Work that restrict the terms of this License or the ability of the
+ recipient of the Work to exercise the rights granted to that recipient
+ under the terms of the License. You may not sublicense the Work. You
+ must keep intact all notices that refer to this License and to the
+ disclaimer of warranties with every copy of the Work You Distribute or
+ Publicly Perform. When You Distribute or Publicly Perform the Work, You
+ may not impose any effective technological measures on the Work that
+ restrict the ability of a recipient of the Work from You to exercise the
+ rights granted to that recipient under the terms of the License. This
+ Section 4(a) applies to the Work as incorporated in a Collection, but
+ this does not require the Collection apart from the Work itself to be
+ made subject to the terms of this License. If You create a Collection,
+ upon notice from any Licensor You must, to the extent practicable,
+ remove from the Collection any credit as required by Section 4(c), as
+ requested. If You create an Adaptation, upon notice from any Licensor
+ You must, to the extent practicable, remove from the Adaptation any
+ credit as required by Section 4(c), as requested.
+ .
+ b. You may Distribute or Publicly Perform an Adaptation only under the
+ terms of: (i) this License; (ii) a later version of this License with
+ the same License Elements as this License; (iii) a Creative Commons
+ jurisdiction license (either this or a later license version) that
+ contains the same License Elements as this License (e.g.,
+ Attribution-ShareAlike 3.0 US)); (iv) a Creative Commons Compatible
+ License. If you license the Adaptation under one of the licenses
+ mentioned in (iv), you must comply with the terms of that license. If
+ you license the Adaptation under the terms of any of the licenses
+ mentioned in (i), (ii) or (iii) (the "Applicable License"), you must
+ comply with the terms of the Applicable License generally and the
+ following provisions: (I) You must include a copy of, or the URI for,
+ the Applicable License with every copy of each Adaptation You Distribute
+ or Publicly Perform; (II) You may not offer or impose any terms on the
+ Adaptation that restrict the terms of the Applicable License or the
+ ability of the recipient of the Adaptation to exercise the rights
+ granted to that recipient under the terms of the Applicable License;
+ (III) You must keep intact all notices that refer to the Applicable
+ License and to the disclaimer of warranties with every copy of the Work
+ as included in the Adaptation You Distribute or Publicly Perform; (IV)
+ when You Distribute or Publicly Perform the Adaptation, You may not
+ impose any effective technological measures on the Adaptation that
+ restrict the ability of a recipient of the Adaptation from You to
+ exercise the rights granted to that recipient under the terms of the
+ Applicable License. This Section 4(b) applies to the Adaptation as
+ incorporated in a Collection, but this does not require the Collection
+ apart from the Adaptation itself to be made subject to the terms of the
+ Applicable License.
+ .
+ c. If You Distribute, or Publicly Perform the Work or any Adaptations or
+ Collections, You must, unless a request has been made pursuant to
+ Section 4(a), keep intact all copyright notices for the Work and
+ provide, reasonable to the medium or means You are utilizing: (i) the
+ name of the Original Author (or pseudonym, if applicable) if supplied,
+ and/or if the Original Author and/or Licensor designate another party or
+ parties (e.g., a sponsor institute, publishing entity, journal) for
+ attribution ("Attribution Parties") in Licensor's copyright notice,
+ terms of service or by other reasonable means, the name of such party or
+ parties; (ii) the title of the Work if supplied; (iii) to the extent
+ reasonably practicable, the URI, if any, that Licensor specifies to be
+ associated with the Work, unless such URI does not refer to the
+ copyright notice or licensing information for the Work; and (iv) ,
+ consistent with Ssection 3(b), in the case of an Adaptation, a credit
+ identifying the use of the Work in the Adaptation (e.g., "French
+ translation of the Work by Original Author," or "Screenplay based on
+ original Work by Original Author"). The credit required by this Section
+ 4(c) may be implemented in any reasonable manner; provided, however,
+ that in the case of a Adaptation or Collection, at a minimum such credit
+ will appear, if a credit for all contributing authors of the Adaptation
+ or Collection appears, then as part of these credits and in a manner at
+ least as prominent as the credits for the other contributing authors.
+ For the avoidance of doubt, You may only use the credit required by this
+ Section for the purpose of attribution in the manner set out above and,
+ by exercising Your rights under this License, You may not implicitly or
+ explicitly assert or imply any connection with, sponsorship or
+ endorsement by the Original Author, Licensor and/or Attribution Parties,
+ as appropriate, of You or Your use of the Work, without the separate,
+ express prior written permission of the Original Author, Licensor and/or
+ Attribution Parties.
+ .
+ d. Except as otherwise agreed in writing by the Licensor or as may be
+ otherwise permitted by applicable law, if You Reproduce, Distribute or
+ Publicly Perform the Work either by itself or as part of any Adaptations
+ or Collections, You must not distort, mutilate, modify or take other
+ derogatory action in relation to the Work which would be prejudicial to
+ the Original Author's honor or reputation. Licensor agrees that in those
+ jurisdictions (e.g. Japan), in which any exercise of the right granted
+ in Section 3(b) of this License (the right to make Adaptations) would be
+ deemed to be a distortion, mutilation, modification or other derogatory
+ action prejudicial to the Original Author's honor and reputation, the
+ Licensor will waive or not assert, as appropriate, this Section, to the
+ fullest extent permitted by the applicable national law, to enable You
+ to reasonably exercise Your right under Section 3(b) of this License
+ (right to make Adaptations) but not otherwise.
+ .
+ 5. Representations, Warranties and Disclaimer
+ .
+ UNLESS OTHERWISE MUTUALLY AGREED TO BY THE PARTIES IN WRITING, LICENSOR
+ OFFERS THE WORK AS-IS AND MAKES NO REPRESENTATIONS OR WARRANTIES OF ANY
+ KIND CONCERNING THE WORK, EXPRESS, IMPLIED, STATUTORY OR OTHERWISE,
+ INCLUDING, WITHOUT LIMITATION, WARRANTIES OF TITLE, MERCHANTIBILITY,
+ FITNESS FOR A PARTICULAR PURPOSE, NONINFRINGEMENT, OR THE ABSENCE OF
+ LATENT OR OTHER DEFECTS, ACCURACY, OR THE PRESENCE OF ABSENCE OF ERRORS,
+ WHETHER OR NOT DISCOVERABLE. SOME JURISDICTIONS DO NOT ALLOW THE
+ EXCLUSION OF IMPLIED WARRANTIES, SO SUCH EXCLUSION MAY NOT APPLY TO YOU.
+ .
+ 6. Limitation on Liability. EXCEPT TO THE EXTENT REQUIRED BY APPLICABLE
+ LAW, IN NO EVENT WILL LICENSOR BE LIABLE TO YOU ON ANY LEGAL THEORY FOR
+ ANY SPECIAL, INCIDENTAL, CONSEQUENTIAL, PUNITIVE OR EXEMPLARY DAMAGES
+ ARISING OUT OF THIS LICENSE OR THE USE OF THE WORK, EVEN IF LICENSOR HAS
+ BEEN ADVISED OF THE POSSIBILITY OF SUCH DAMAGES.
+ .
+ 7. Termination
+ .
+ a. This License and the rights granted hereunder will terminate
+ automatically upon any breach by You of the terms of this License.
+ Individuals or entities who have received Adaptations or Collections
+ from You under this License, however, will not have their licenses
+ terminated provided such individuals or entities remain in full
+ compliance with those licenses. Sections 1, 2, 5, 6, 7, and 8 will
+ survive any termination of this License.
+ .
+ b. Subject to the above terms and conditions, the license granted here
+ is perpetual (for the duration of the applicable copyright in the Work).
+ Notwithstanding the above, Licensor reserves the right to release the
+ Work under different license terms or to stop distributing the Work at
+ any time; provided, however that any such election will not serve to
+ withdraw this License (or any other license that has been, or is
+ required to be, granted under the terms of this License), and this
+ License will continue in full force and effect unless terminated as
+ stated above.
+ .
+ 8. Miscellaneous
+ .
+ a. Each time You Distribute or Publicly Perform the Work or a
+ Collection, the Licensor offers to the recipient a license to the Work
+ on the same terms and conditions as the license granted to You under
+ this License.
+ .
+ b. Each time You Distribute or Publicly Perform an Adaptation, Licensor
+ offers to the recipient a license to the original Work on the same terms
+ and conditions as the license granted to You under this License.
+ .
+ c. If any provision of this License is invalid or unenforceable under
+ applicable law, it shall not affect the validity or enforceability of
+ the remainder of the terms of this License, and without further action
+ by the parties to this agreement, such provision shall be reformed to
+ the minimum extent necessary to make such provision valid and
+ enforceable.
+ .
+ d. No term or provision of this License shall be deemed waived and no
+ breach consented to unless such waiver or consent shall be in writing
+ and signed by the party to be charged with such waiver or consent.
+ .
+ e. This License constitutes the entire agreement between the parties
+ with respect to the Work licensed here. There are no understandings,
+ agreements or representations with respect to the Work not specified
+ here. Licensor shall not be bound by any additional provisions that may
+ appear in any communication from You. This License may not be modified
+ without the mutual written agreement of the Licensor and You.
+ .
+ f. The rights granted under, and the subject matter referenced, in this
+ License were drafted utilizing the terminology of the Berne Convention
+ for the Protection of Literary and Artistic Works (as amended on
+ September 28, 1979), the Rome Convention of 1961, the WIPO Copyright
+ Treaty of 1996, the WIPO Performances and Phonograms Treaty of 1996 and
+ the Universal Copyright Convention (as revised on July 24, 1971). These
+ rights and subject matter take effect in the relevant jurisdiction in
+ which the License terms are sought to be enforced according to the
+ corresponding provisions of the implementation of those treaty
+ provisions in the applicable national law. If the standard suite of
+ rights granted under applicable copyright law includes additional rights
+ not granted under this License, such additional rights are deemed to be
+ included in the License; this License is not intended to restrict the
+ license of any rights under applicable law.
+
diff --git a/debian/docs b/debian/docs
new file mode 100644
index 0000000..4e8727a
--- /dev/null
+++ b/debian/docs
@@ -0,0 +1,3 @@
+doc/
+README
+
diff --git a/debian/gbp.conf b/debian/gbp.conf
new file mode 100644
index 0000000..f06152e
--- /dev/null
+++ b/debian/gbp.conf
@@ -0,0 +1,12 @@
+# Settings for Debian Tryton Maintainer repositories
+# for usage with git-buildpackage
+
+[DEFAULT]
+debian-branch = debian
+pristine-tar = True
+
+[git-buildpackage]
+ignore-new = True
+# Use export-dir at your discretion to avoid git-buildpackage messing
+# your git repository
+#export-dir = ../build-area/
diff --git a/debian/pydist-overrides b/debian/pydist-overrides
new file mode 100644
index 0000000..5c61cb3
--- /dev/null
+++ b/debian/pydist-overrides
@@ -0,0 +1 @@
+trytond_health tryton-modules-health
diff --git a/debian/rules b/debian/rules
new file mode 100755
index 0000000..00a4d07
--- /dev/null
+++ b/debian/rules
@@ -0,0 +1,23 @@
+#!/usr/bin/make -f
+
+# Tryton dependency version
+TMAJ := $(shell grep "^major_version, minor_version =" setup.py | sed "s/[^0-9]//g;" | cut -c -1)
+TMIN := $(shell grep "^major_version, minor_version =" setup.py | sed "s/[^0-9]//g;" | cut -c 2-)
+TMAJOR := $(TMAJ).$(TMIN)
+TDEV := $(TMAJ).$(shell echo $$(($(TMIN) + 1)))
+# GnuHealth dependency version
+MAJ := $(shell python setup.py --version | awk -F "." '{print $$1}')
+MIN := $(shell python setup.py --version | awk -F "." '{print $$2}')
+MAJOR := $(MAJ).$(MIN)
+DEV := $(MAJ).$(shell echo $$(($(MIN) + 1)))
+
+# Don't run tests for Tryton modules, they try to download dependencies from pypi
+export PYBUILD_DISABLE_python2.7=test
+
+%:
+ dh ${@} --with python2 --buildsystem=pybuild
+
+override_dh_gencontrol:
+ dh_gencontrol -- -Vversion:major="$(MAJOR)" -Vversion:dev="$(DEV)" \
+ -Vversion:tmajor="$(TMAJOR)" -Vversion:tdev="$(TDEV)"
+
diff --git a/debian/source/format b/debian/source/format
new file mode 100644
index 0000000..163aaf8
--- /dev/null
+++ b/debian/source/format
@@ -0,0 +1 @@
+3.0 (quilt)
diff --git a/debian/watch b/debian/watch
new file mode 100644
index 0000000..6a52de1
--- /dev/null
+++ b/debian/watch
@@ -0,0 +1,3 @@
+version=3
+opts=uversionmangle=s/(rc|a|b|c)/~$1/ \
+http://pypi.debian.net/trytond_health_genetics/trytond_health_genetics-(.+)\.(?:zip|tgz|tbz|txz|(?:tar\.(?:gz|bz2|xz)))
\ No newline at end of file
diff --git a/doc/index.rst b/doc/index.rst
new file mode 100644
index 0000000..ee91dc6
--- /dev/null
+++ b/doc/index.rst
@@ -0,0 +1,10 @@
+GNU Health Genetics Module
+##########################
+
+Family history and genetic risks.
+
+This module add support to:
+
+ * Hereditary risks, family history and genetic disorders.
+
+ * NCBI and GeneCards information, more than 4200 genes associated to diseases
diff --git a/health_genetics.py b/health_genetics.py
new file mode 100644
index 0000000..ca3aa14
--- /dev/null
+++ b/health_genetics.py
@@ -0,0 +1,120 @@
+# -*- coding: utf-8 -*-
+##############################################################################
+#
+# GNU Health: The Free Health and Hospital Information System
+# Copyright (C) 2008-2015 Luis Falcon <lfalcon at gnusolidario.org>
+# Copyright (C) 2011-2015 GNU Solidario <health at gnusolidario.org>
+#
+#
+# This program is free software: you can redistribute it and/or modify
+# it under the terms of the GNU General Public License as published by
+# the Free Software Foundation, either version 3 of the License, or
+# (at your option) any later version.
+#
+# This program is distributed in the hope that it will be useful,
+# but WITHOUT ANY WARRANTY; without even the implied warranty of
+# MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the
+# GNU General Public License for more details.
+#
+# You should have received a copy of the GNU General Public License
+# along with this program. If not, see <http://www.gnu.org/licenses/>.
+#
+##############################################################################
+from trytond.model import ModelView, ModelSQL, fields
+
+
+__all__ = ['DiseaseGene', 'PatientGeneticRisk', 'FamilyDiseases',
+ 'GnuHealthPatient']
+
+
+class DiseaseGene(ModelSQL, ModelView):
+ 'Disease Genes'
+ __name__ = 'gnuhealth.disease.gene'
+
+ name = fields.Char('Official Symbol', required=True,select=True)
+ long_name = fields.Char('Official Long Name', select=True)
+ gene_id = fields.Char('Gene ID',
+ help="default code from NCBI Entrez database.", select=True)
+ chromosome = fields.Char('Affected Chromosome',
+ help="Name of the affected chromosome", select=True)
+ location = fields.Char('Location', help="Locus of the chromosome")
+ dominance = fields.Selection([
+ (None, ''),
+ ('d', 'dominant'),
+ ('r', 'recessive'),
+ ], 'Dominance', select=True)
+ info = fields.Text('Information', help="Extra Information")
+
+ @classmethod
+ def __setup__(cls):
+ super(DiseaseGene, cls).__setup__()
+ cls._sql_constraints = [
+ ('name_uniq', 'UNIQUE(name)',
+ 'The Official Symbol name must be unique !'),
+ ]
+
+ def get_rec_name(self, name):
+ return self.name + ':' + self.long_name
+
+ @classmethod
+ def search_rec_name(cls, name, clause):
+ """ Search for the official and long name"""
+ field = None
+ for field in ('name', 'long_name'):
+ parties = cls.search([(field,) + tuple(clause[1:])], limit=1)
+ if parties:
+ break
+ if parties:
+ return [(field,) + tuple(clause[1:])]
+ return [(cls._rec_name,) + tuple(clause[1:])]
+
+
+class PatientGeneticRisk(ModelSQL, ModelView):
+ 'Patient Genetic Risks'
+ __name__ = 'gnuhealth.patient.genetic.risk'
+
+ patient = fields.Many2One('gnuhealth.patient', 'Patient', select=True)
+ disease_gene = fields.Many2One('gnuhealth.disease.gene',
+ 'Disease Gene', required=True)
+ notes = fields.Char("Notes")
+
+class FamilyDiseases(ModelSQL, ModelView):
+ 'Family Diseases'
+ __name__ = 'gnuhealth.patient.family.diseases'
+
+ patient = fields.Many2One('gnuhealth.patient', 'Patient', select=True)
+ name = fields.Many2One('gnuhealth.pathology', 'Disease', required=True)
+ xory = fields.Selection([
+ (None, ''),
+ ('m', 'Maternal'),
+ ('f', 'Paternal'),
+ ('s', 'Sibling'),
+ ], 'Maternal or Paternal', select=True)
+
+ relative = fields.Selection([
+ ('mother', 'Mother'),
+ ('father', 'Father'),
+ ('brother', 'Brother'),
+ ('sister', 'Sister'),
+ ('aunt', 'Aunt'),
+ ('uncle', 'Uncle'),
+ ('nephew', 'Nephew'),
+ ('niece', 'Niece'),
+ ('grandfather', 'Grandfather'),
+ ('grandmother', 'Grandmother'),
+ ('cousin', 'Cousin'),
+ ], 'Relative',
+ help="First degree = siblings, mother and father; second degree = "
+ "Uncles, nephews and Nieces; third degree = Grandparents and cousins",
+ required=True)
+
+
+class GnuHealthPatient (ModelSQL, ModelView):
+ 'Add to the Medical patient_data class (gnuhealth.patient) the genetic ' \
+ 'and family risks'
+ __name__ = 'gnuhealth.patient'
+
+ genetic_risks = fields.One2Many('gnuhealth.patient.genetic.risk',
+ 'patient', 'Genetic Risks')
+ family_history = fields.One2Many('gnuhealth.patient.family.diseases',
+ 'patient', 'Family History')
diff --git a/health_genetics_view.xml b/health_genetics_view.xml
new file mode 100644
index 0000000..3e0e0e7
--- /dev/null
+++ b/health_genetics_view.xml
@@ -0,0 +1,94 @@
+<?xml version="1.0"?>
+<tryton>
+ <data>
+
+<!-- Add Genetics icon -->
+
+ <record model="ir.ui.icon" id="gnuhealth_dna_icon">
+ <field name="name">icon-dna</field>
+ <field name="path">icons/dna.svg</field>
+ </record>
+
+ <menuitem name="Genetics" parent="health.gnuhealth_conf_menu"
+ id="gnuhealth_conf_genetics" icon="icon-dna"/>
+
+<!-- Add other relevant icons -->
+
+ <record model="ir.ui.icon" id="gnuhealth_list_icon">
+ <field name="name">gnuhealth-list</field>
+ <field name="path">../health/icons/tryton-list.svg</field>
+ </record>
+
+<!-- Genetic Risks -->
+
+ <record model="ir.ui.view" id="gnuhealth_disease_gene_view">
+ <field name="model">gnuhealth.disease.gene</field>
+ <field name="type">form</field>
+ <field name="name">gnuhealth_disease_gene</field>
+ </record>
+
+ <record model="ir.ui.view" id="gnuhealth_disease_gene_tree">
+ <field name="model">gnuhealth.disease.gene</field>
+ <field name="type">tree</field>
+ <field name="name">gnuhealth_disease_gene_tree</field>
+ </record>
+
+ <record model="ir.action.act_window" id="gnuhealth_action_disease_gene">
+ <field name="name">Disease Genes</field>
+ <field name="res_model">gnuhealth.disease.gene</field>
+ </record>
+
+ <record model="ir.action.act_window.view" id="act_disease_gene_list_view">
+ <field name="sequence" eval="10"/>
+ <field name="view" ref="gnuhealth_disease_gene_tree"/>
+ <field name="act_window" ref="gnuhealth_action_disease_gene"/>
+ </record>
+ <record model="ir.action.act_window.view" id="act_disease_gene_form_view">
+ <field name="sequence" eval="20"/>
+ <field name="view" ref="gnuhealth_disease_gene_view"/>
+ <field name="act_window" ref="gnuhealth_action_disease_gene"/>
+ </record>
+
+ <menuitem parent="gnuhealth_conf_genetics"
+ action="gnuhealth_action_disease_gene"
+ id="gnuhealth_conf_disease_genes" icon="gnuhealth-list"/>
+
+<!-- Patient Genetic Risk -->
+
+ <record model="ir.ui.view" id="gnuhealth_genetic_risk_view">
+ <field name="model">gnuhealth.patient.genetic.risk</field>
+ <field name="type">form</field>
+ <field name="name">gnuhealth_genetic_risk</field>
+ </record>
+
+ <record model="ir.ui.view" id="gnuhealth_genetic_risk_tree">
+ <field name="model">gnuhealth.patient.genetic.risk</field>
+ <field name="type">tree</field>
+ <field name="name">gnuhealth_genetic_risk_tree</field>
+ </record>
+
+<!-- Family Diseases -->
+
+ <record model="ir.ui.view" id="gnuhealth_family_diseases_view">
+ <field name="model">gnuhealth.patient.family.diseases</field>
+ <field name="type">form</field>
+ <field name="name">gnuhealth_family_diseases</field>
+ </record>
+
+ <record model="ir.ui.view" id="gnuhealth_family_diseases_tree">
+ <field name="model">gnuhealth.patient.family.diseases</field>
+ <field name="type">tree</field>
+ <field name="name">gnuhealth_family_diseases_tree</field>
+ </record>
+
+<!-- Include Family History and Genetic Risks on the patient chart -->
+
+ <record model="ir.ui.view" id="gnuhealth_patient_view">
+ <field name="model">gnuhealth.patient</field>
+ <field name="inherit" ref="health.gnuhealth_patient_view_form" />
+ <field name="type">form</field>
+ <field name="name">gnuhealth_patient</field>
+ </record>
+
+ </data>
+</tryton>
diff --git a/icons/README b/icons/README
new file mode 100644
index 0000000..154179d
--- /dev/null
+++ b/icons/README
@@ -0,0 +1 @@
+dna : Leonardo D'Acchille - GNU Solidario (CC-SA 3.0)
diff --git a/icons/dna.svg b/icons/dna.svg
new file mode 100644
index 0000000..14ec30e
--- /dev/null
+++ b/icons/dna.svg
@@ -0,0 +1,141 @@
+<?xml version="1.0" encoding="iso-8859-1"?><!DOCTYPE svg PUBLIC "-//W3C//DTD SVG 1.1//EN" "http://www.w3.org/Graphics/SVG/1.1/DTD/svg11.dtd">
+<svg version="1.1" id="Capa_1" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink" x="0px" y="0px"
+ width="97px" height="97px" viewBox="0 0 97 97" style="enable-background:new 0 0 97 97;" xml:space="preserve">
+<linearGradient id="SVGID_1_" gradientUnits="userSpaceOnUse" x1="104.79" y1="60.1807" x2="62.9125" y2="97.8874">
+ <stop offset="0.4784" style="stop-color:#FABF73"/>
+ <stop offset="0.5747" style="stop-color:#FCC989"/>
+ <stop offset="0.7771" style="stop-color:#FEE2C0"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<polygon style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_1_);" points="69.717,88.849 89.502,69.545 93.304,73.436
+ 73.518,92.738 "/>
+<linearGradient id="SVGID_2_" gradientUnits="userSpaceOnUse" x1="84.4609" y1="59.1045" x2="46.5585" y2="97.0069">
+ <stop offset="0.1176" style="stop-color:#FABF73"/>
+ <stop offset="0.2804" style="stop-color:#FCC989"/>
+ <stop offset="0.623" style="stop-color:#FEE2C0"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<polygon style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_2_);" points="57.609,82.096 82.464,57.242 86.324,61.103
+ 61.471,85.955 "/>
+<linearGradient id="SVGID_3_" gradientUnits="userSpaceOnUse" x1="70.8467" y1="53.4063" x2="43.6719" y2="77.0289">
+ <stop offset="0" style="stop-color:#FABF73"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<polygon style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_3_);" points="51.815,67.656 67.981,51.008 71.872,54.808
+ 55.706,71.457 "/>
+<linearGradient id="SVGID_4_" gradientUnits="userSpaceOnUse" x1="35.144" y1="46.3711" x2="76.9528" y2="12.515">
+ <stop offset="0" style="stop-color:#FABF73"/>
+ <stop offset="0.1487" style="stop-color:#FCCF97"/>
+ <stop offset="0.3369" style="stop-color:#FEE1BD"/>
+ <stop offset="0.5206" style="stop-color:#FFEEDB"/>
+ <stop offset="0.6961" style="stop-color:#FFF8EF"/>
+ <stop offset="0.8598" style="stop-color:#FFFDFB"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<polygon style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_4_);" points="30.447,48.146 48.303,30.773 52.104,34.664
+ 34.248,52.038 "/>
+<linearGradient id="SVGID_5_" gradientUnits="userSpaceOnUse" x1="18.0552" y1="43.7412" x2="62.4407" y2="5.1574">
+ <stop offset="0.1894" style="stop-color:#FABF73"/>
+ <stop offset="0.3136" style="stop-color:#FDD3A0"/>
+ <stop offset="0.4498" style="stop-color:#FEE6CA"/>
+ <stop offset="0.571" style="stop-color:#FFF4E7"/>
+ <stop offset="0.6713" style="stop-color:#FFFCF9"/>
+ <stop offset="0.7384" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<polygon style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_5_);" points="15.358,44.156 44.554,15.441 48.37,19.317
+ 19.173,48.032 "/>
+<linearGradient id="SVGID_6_" gradientUnits="userSpaceOnUse" x1="17.9004" y1="26.9063" x2="53.5078" y2="-9.9663">
+ <stop offset="0" style="stop-color:#FABF73"/>
+ <stop offset="0.2262" style="stop-color:#FDD3A0"/>
+ <stop offset="0.4742" style="stop-color:#FEE6CA"/>
+ <stop offset="0.695" style="stop-color:#FFF4E7"/>
+ <stop offset="0.8778" style="stop-color:#FFFCF9"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<polygon style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_6_);" points="3.94,36.616 37.24,3.799 41.071,7.659
+ 7.771,40.477 "/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="51.437" cy="51.119" r="7.678"/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="33.312" cy="50.008" r="6.483"/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="69.542" cy="53.229" r="6.483"/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="17.627" cy="46.213" r="5.617"/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="84.273" cy="59.098" r="5.618"/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="6.159" cy="38.751" r="4.777"/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="91.282" cy="71.078" r="4.777"/>
+<linearGradient id="SVGID_7_" gradientUnits="userSpaceOnUse" x1="51.5693" y1="56.2266" x2="51.1965" y2="45.5497">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_7_);" cx="51.388" cy="51.071" r="5.527"/>
+<linearGradient id="SVGID_8_" gradientUnits="userSpaceOnUse" x1="33.3467" y1="52.123" x2="33.187" y2="47.5495">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_8_);" cx="33.271" cy="49.968" r="3.986"/>
+<linearGradient id="SVGID_9_" gradientUnits="userSpaceOnUse" x1="69.6318" y1="56.9092" x2="69.3628" y2="49.2058">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_9_);" cx="69.502" cy="53.188" r="3.986"/>
+<linearGradient id="SVGID_10_" gradientUnits="userSpaceOnUse" x1="17.6904" y1="48.9766" x2="17.4881" y2="43.1814">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_10_);" cx="17.592" cy="46.178" r="3"/>
+<linearGradient id="SVGID_11_" gradientUnits="userSpaceOnUse" x1="84.3359" y1="61.8623" x2="84.1335" y2="56.0662">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_11_);" cx="84.238" cy="59.063" r="3"/>
+<linearGradient id="SVGID_12_" gradientUnits="userSpaceOnUse" x1="6.1953" y1="40.5879" x2="6.0604" y2="36.7252">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_12_);" cx="6.129" cy="38.722" r="2"/>
+<linearGradient id="SVGID_13_" gradientUnits="userSpaceOnUse" x1="91.3184" y1="72.9141" x2="91.1835" y2="69.0514">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_13_);" cx="91.253" cy="71.048" r="1.999"/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="51.433" cy="51.2" r="7.678"/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="50.321" cy="33.076" r="6.484"/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="53.542" cy="69.307" r="6.483"/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="46.527" cy="17.391" r="5.618"/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="59.411" cy="84.038" r="5.618"/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="39.065" cy="5.924" r="4.777"/>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:#46ACB2;stroke:#08828B;stroke-width:2.0001;stroke-linecap:round;stroke-linejoin:round;stroke-miterlimit:22.9256;" cx="71.392" cy="91.047" r="4.777"/>
+<linearGradient id="SVGID_14_" gradientUnits="userSpaceOnUse" x1="50.04" y1="55.292" x2="53.0102" y2="46.1508">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_14_);" cx="51.384" cy="51.152" r="4.982"/>
+<linearGradient id="SVGID_15_" gradientUnits="userSpaceOnUse" x1="49.2051" y1="36.3467" x2="51.5813" y2="29.0335">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_15_);" cx="50.28" cy="33.035" r="3.985"/>
+<linearGradient id="SVGID_16_" gradientUnits="userSpaceOnUse" x1="52.4248" y1="72.5781" x2="54.8011" y2="65.2647">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_16_);" cx="53.501" cy="69.267" r="3.986"/>
+<linearGradient id="SVGID_17_" gradientUnits="userSpaceOnUse" x1="45.6821" y1="19.8486" x2="47.4703" y2="14.3452">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_17_);" cx="46.492" cy="17.356" r="3"/>
+<linearGradient id="SVGID_18_" gradientUnits="userSpaceOnUse" x1="58.5664" y1="86.4951" x2="60.3543" y2="80.9926">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_18_);" cx="59.376" cy="84.003" r="2.998"/>
+<linearGradient id="SVGID_19_" gradientUnits="userSpaceOnUse" x1="38.4951" y1="7.5557" x2="39.6874" y2="3.8862">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_19_);" cx="39.035" cy="5.894" r="2"/>
+<linearGradient id="SVGID_20_" gradientUnits="userSpaceOnUse" x1="70.8223" y1="92.6787" x2="72.0146" y2="89.0092">
+ <stop offset="0" style="stop-color:#34A6AE"/>
+ <stop offset="1" style="stop-color:#FFFFFF"/>
+</linearGradient>
+<circle style="fill-rule:evenodd;clip-rule:evenodd;fill:url(#SVGID_20_);" cx="71.361" cy="91.018" r="1.999"/>
+</svg>
diff --git a/locale/el_GR.po b/locale/el_GR.po
new file mode 100644
index 0000000..054db27
--- /dev/null
+++ b/locale/el_GR.po
@@ -0,0 +1,295 @@
+#
+# Translators:
+# Efstathios Iosifidis <iefstathios at gmail.com>, 2012
+# kvisitor <kvisitor at gnugr.org>, 2011, 2012
+msgid ""
+msgstr ""
+"Project-Id-Version: GNU Health\n"
+"Report-Msgid-Bugs-To: https://savannah.gnu.org/bugs/?group=health\n"
+"POT-Creation-Date: 2015-01-27 11:17+0000\n"
+"PO-Revision-Date: 2015-01-13 14:54+0000\n"
+"Last-Translator: Bruno Villasanti <bvillasanti at thymbra.com>\n"
+"Language-Team: Greek (http://www.transifex.com/projects/p/GNU_Health/language/el/)\n"
+"MIME-Version: 1.0\n"
+"Content-Type: text/plain; charset=UTF-8\n"
+"Content-Transfer-Encoding: 8bit\n"
+"Language: el\n"
+"Plural-Forms: nplurals=2; plural=(n != 1);\n"
+
+msgctxt "error:gnuhealth.disease.gene:"
+msgid "The Official Symbol name must be unique !"
+msgstr ""
+
+msgctxt "field:gnuhealth.disease.gene,chromosome:"
+msgid "Affected Chromosome"
+msgstr "Εμπλεκόμενο γονίδιο"
+
+msgctxt "field:gnuhealth.disease.gene,create_date:"
+msgid "Create Date"
+msgstr "Δημιουργία ημερομηνίας"
+
+msgctxt "field:gnuhealth.disease.gene,create_uid:"
+msgid "Create User"
+msgstr "Δημιουργία Χρήστη"
+
+msgctxt "field:gnuhealth.disease.gene,dominance:"
+msgid "Dominance"
+msgstr "Κυριαρχία"
+
+msgctxt "field:gnuhealth.disease.gene,gene_id:"
+msgid "Gene ID"
+msgstr "Κωδικός ID του γονιδίου"
+
+msgctxt "field:gnuhealth.disease.gene,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.disease.gene,info:"
+msgid "Information"
+msgstr "Πληροφορίες"
+
+msgctxt "field:gnuhealth.disease.gene,location:"
+msgid "Location"
+msgstr "Τοποθεσία"
+
+msgctxt "field:gnuhealth.disease.gene,long_name:"
+msgid "Official Long Name"
+msgstr "Επίσημο πλήρες όνομα"
+
+msgctxt "field:gnuhealth.disease.gene,name:"
+msgid "Official Symbol"
+msgstr "Επίσημο σύμβολο"
+
+msgctxt "field:gnuhealth.disease.gene,rec_name:"
+msgid "Name"
+msgstr "Όνομα"
+
+msgctxt "field:gnuhealth.disease.gene,write_date:"
+msgid "Write Date"
+msgstr "Γράψτε την Ημερομηνία"
+
+msgctxt "field:gnuhealth.disease.gene,write_uid:"
+msgid "Write User"
+msgstr "Γράψτε τον Χρήστη"
+
+msgctxt "field:gnuhealth.patient,family_history:"
+msgid "Family History"
+msgstr "Οικογενειακό Ιστορικό"
+
+msgctxt "field:gnuhealth.patient,genetic_risks:"
+msgid "Genetic Risks"
+msgstr "Γενετικοί κίνδυνοι"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_date:"
+msgid "Create Date"
+msgstr "Δημιουργία Ημερομηνίας"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_uid:"
+msgid "Create User"
+msgstr "Δημιουργία Χρήστη"
+
+msgctxt "field:gnuhealth.patient.family.diseases,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.family.diseases,name:"
+msgid "Disease"
+msgstr "Νόσος;"
+
+msgctxt "field:gnuhealth.patient.family.diseases,patient:"
+msgid "Patient"
+msgstr "Ασθενής"
+
+msgctxt "field:gnuhealth.patient.family.diseases,rec_name:"
+msgid "Name"
+msgstr "Όνομα"
+
+msgctxt "field:gnuhealth.patient.family.diseases,relative:"
+msgid "Relative"
+msgstr "Συγγενής"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_date:"
+msgid "Write Date"
+msgstr "Γράψτε την Ημερομηνία"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_uid:"
+msgid "Write User"
+msgstr "Γράψτε τον Χρήστη"
+
+msgctxt "field:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal or Paternal"
+msgstr "Από τη μεριά της Μητέρας ή του Πατέρα"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_date:"
+msgid "Create Date"
+msgstr "Δημιουργία ημερομηνίας"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_uid:"
+msgid "Create User"
+msgstr "Δημιουργία Χρήστη"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,disease_gene:"
+msgid "Disease Gene"
+msgstr "Γονίδιο της νόσου"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,notes:"
+msgid "Notes"
+msgstr "Σημειώσεις"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,patient:"
+msgid "Patient"
+msgstr "Ασθενής"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,rec_name:"
+msgid "Name"
+msgstr "Όνομα"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_date:"
+msgid "Write Date"
+msgstr "Γράψτε την Ημερομηνία"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_uid:"
+msgid "Write User"
+msgstr "Γράψτε τον Χρήστη"
+
+msgctxt "help:gnuhealth.disease.gene,chromosome:"
+msgid "Name of the affected chromosome"
+msgstr "Όνομα του εμπλεκόμενου γονιδίου"
+
+msgctxt "help:gnuhealth.disease.gene,gene_id:"
+msgid "default code from NCBI Entrez database."
+msgstr "Προκαθορισμένο όνομα στη βάση δεδομένων "
+
+msgctxt "help:gnuhealth.disease.gene,info:"
+msgid "Extra Information"
+msgstr "Πρόσθετες πληροφορίες"
+
+msgctxt "help:gnuhealth.disease.gene,location:"
+msgid "Locus of the chromosome"
+msgstr "Locus του χρωμοσώματος"
+
+msgctxt "help:gnuhealth.patient.family.diseases,relative:"
+msgid ""
+"First degree = siblings, mother and father; second degree = Uncles, nephews "
+"and Nieces; third degree = Grandparents and cousins"
+msgstr "Πρώου βαθμού = αδέλφια, μητέρα και πατέρας; Δευτέρου βαθμού = θείοι, θείες, ανήψια και ανεψιές / Τρίτου βαθμού = Παπούδες και ξαδέλφια"
+
+msgctxt "model:gnuhealth.disease.gene,name:"
+msgid "Disease Genes"
+msgstr "Γονίδια της νόσου"
+
+msgctxt "model:gnuhealth.patient.family.diseases,name:"
+msgid "Family Diseases"
+msgstr "Οικογενειακά Νοσήματα"
+
+msgctxt "model:gnuhealth.patient.genetic.risk,name:"
+msgid "Patient Genetic Risks"
+msgstr "Γενετικοί κίνδυνοι του ασθενούς"
+
+msgctxt "model:ir.action,name:gnuhealth_action_disease_gene"
+msgid "Disease Genes"
+msgstr "Γονίδια ασθενειών"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_disease_genes"
+msgid "Disease Genes"
+msgstr "Γονίδια ασθενειών"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_genetics"
+msgid "Genetics"
+msgstr "Γενετική"
+
+msgctxt "model:res.group,name:group_health_genetics_admin"
+msgid "Health Genetics Administration"
+msgstr "Διαχείριση γενετικής υγείας"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "dominant"
+msgstr "κυρίαρχο"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "recessive"
+msgstr "υποτελές"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Aunt"
+msgstr "Θεία"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Brother"
+msgstr "Αδερφός"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Cousin"
+msgstr "Ξάδερφος"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Father"
+msgstr "Πατέρας"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandfather"
+msgstr "Παππούς"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandmother"
+msgstr "Γιαγιά"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Mother"
+msgstr "Μητέρα"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Nephew"
+msgstr "Ανηψιός"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Niece"
+msgstr "Ανηψιά"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Sister"
+msgstr "Αδελφή"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Uncle"
+msgstr "Θείος"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal"
+msgstr "Από τη μεριά της μητέρας"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Paternal"
+msgstr "Από τη μεριά του πατέρα"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Sibling"
+msgstr ""
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Disease Genes"
+msgstr "Γονίδια νόσου"
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Medical Genetic Risks"
+msgstr "Ιατρικοί κίνδυνοι γενετικής"
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Genetic Family History"
+msgstr ""
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Patient Family History"
+msgstr ""
+
+msgctxt "view:gnuhealth.patient.genetic.risk:"
+msgid "Patient Genetic Risks"
+msgstr "Γενετικοί κίνδυνοι ασθενούς"
+
+msgctxt "view:gnuhealth.patient:"
+msgid "Genetics"
+msgstr "Γενετική"
diff --git a/locale/es_ES.po b/locale/es_ES.po
new file mode 100644
index 0000000..c3ad3b6
--- /dev/null
+++ b/locale/es_ES.po
@@ -0,0 +1,298 @@
+#
+# Translators:
+# Bruno Villasanti <bvillasanti at thymbra.com>, 2014-2015
+# cristina <cmelgosa at thymbra.com>, 2012
+# cristina <cmelgosa at thymbra.com>, 2012
+# Luis Falcon <lfalcon at gnusolidario.org>, 2012
+# Luis Falcon <lfalcon at gnusolidario.org>, 2011-2012
+msgid ""
+msgstr ""
+"Project-Id-Version: GNU Health\n"
+"Report-Msgid-Bugs-To: https://savannah.gnu.org/bugs/?group=health\n"
+"POT-Creation-Date: 2015-01-27 11:17+0000\n"
+"PO-Revision-Date: 2015-01-30 17:11+0000\n"
+"Last-Translator: Bruno Villasanti <bvillasanti at thymbra.com>\n"
+"Language-Team: Spanish (http://www.transifex.com/projects/p/GNU_Health/language/es/)\n"
+"MIME-Version: 1.0\n"
+"Content-Type: text/plain; charset=UTF-8\n"
+"Content-Transfer-Encoding: 8bit\n"
+"Language: es\n"
+"Plural-Forms: nplurals=2; plural=(n != 1);\n"
+
+msgctxt "error:gnuhealth.disease.gene:"
+msgid "The Official Symbol name must be unique !"
+msgstr "¡El Símbolo oficial debe ser único!"
+
+msgctxt "field:gnuhealth.disease.gene,chromosome:"
+msgid "Affected Chromosome"
+msgstr "Cromosoma afectado"
+
+msgctxt "field:gnuhealth.disease.gene,create_date:"
+msgid "Create Date"
+msgstr "Fecha creación"
+
+msgctxt "field:gnuhealth.disease.gene,create_uid:"
+msgid "Create User"
+msgstr "Usuario creación"
+
+msgctxt "field:gnuhealth.disease.gene,dominance:"
+msgid "Dominance"
+msgstr "Dominancia"
+
+msgctxt "field:gnuhealth.disease.gene,gene_id:"
+msgid "Gene ID"
+msgstr "ID del gen"
+
+msgctxt "field:gnuhealth.disease.gene,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.disease.gene,info:"
+msgid "Information"
+msgstr "Información"
+
+msgctxt "field:gnuhealth.disease.gene,location:"
+msgid "Location"
+msgstr "Ubicación"
+
+msgctxt "field:gnuhealth.disease.gene,long_name:"
+msgid "Official Long Name"
+msgstr "Nombre largo oficial"
+
+msgctxt "field:gnuhealth.disease.gene,name:"
+msgid "Official Symbol"
+msgstr "Símbolo oficial"
+
+msgctxt "field:gnuhealth.disease.gene,rec_name:"
+msgid "Name"
+msgstr "Nombre"
+
+msgctxt "field:gnuhealth.disease.gene,write_date:"
+msgid "Write Date"
+msgstr "Fecha modificación"
+
+msgctxt "field:gnuhealth.disease.gene,write_uid:"
+msgid "Write User"
+msgstr "Usuario modificación"
+
+msgctxt "field:gnuhealth.patient,family_history:"
+msgid "Family History"
+msgstr "Historial Familiar"
+
+msgctxt "field:gnuhealth.patient,genetic_risks:"
+msgid "Genetic Risks"
+msgstr "Riesgos genéticos"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_date:"
+msgid "Create Date"
+msgstr "Fecha creación"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_uid:"
+msgid "Create User"
+msgstr "Usuario creación"
+
+msgctxt "field:gnuhealth.patient.family.diseases,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.family.diseases,name:"
+msgid "Disease"
+msgstr "Enfermedad"
+
+msgctxt "field:gnuhealth.patient.family.diseases,patient:"
+msgid "Patient"
+msgstr "Paciente"
+
+msgctxt "field:gnuhealth.patient.family.diseases,rec_name:"
+msgid "Name"
+msgstr "Nombre"
+
+msgctxt "field:gnuhealth.patient.family.diseases,relative:"
+msgid "Relative"
+msgstr "Pariente"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_date:"
+msgid "Write Date"
+msgstr "Fecha modificación"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_uid:"
+msgid "Write User"
+msgstr "Usuario modificación"
+
+msgctxt "field:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal or Paternal"
+msgstr "Materno o paterno"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_date:"
+msgid "Create Date"
+msgstr "Fecha creación"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_uid:"
+msgid "Create User"
+msgstr "Usuario creación"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,disease_gene:"
+msgid "Disease Gene"
+msgstr "Gen Patológico"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,notes:"
+msgid "Notes"
+msgstr "Notas"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,patient:"
+msgid "Patient"
+msgstr "Paciente"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,rec_name:"
+msgid "Name"
+msgstr "Nombre"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_date:"
+msgid "Write Date"
+msgstr "Fecha modificación"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_uid:"
+msgid "Write User"
+msgstr "Usuario modificación"
+
+msgctxt "help:gnuhealth.disease.gene,chromosome:"
+msgid "Name of the affected chromosome"
+msgstr "Nombre del cromosoma afectado"
+
+msgctxt "help:gnuhealth.disease.gene,gene_id:"
+msgid "default code from NCBI Entrez database."
+msgstr "Código predeterminado de la base de datos NCBI Entrez."
+
+msgctxt "help:gnuhealth.disease.gene,info:"
+msgid "Extra Information"
+msgstr "Información adicional"
+
+msgctxt "help:gnuhealth.disease.gene,location:"
+msgid "Locus of the chromosome"
+msgstr "Locus del cromosoma"
+
+msgctxt "help:gnuhealth.patient.family.diseases,relative:"
+msgid ""
+"First degree = siblings, mother and father; second degree = Uncles, nephews "
+"and Nieces; third degree = Grandparents and cousins"
+msgstr "Primer nivel = hermano/a, madre y padre; segundo nivel = Tíos, sobrinos y sobrinas; tercer nivel = abuelos y primos"
+
+msgctxt "model:gnuhealth.disease.gene,name:"
+msgid "Disease Genes"
+msgstr "Genes patológicos"
+
+msgctxt "model:gnuhealth.patient.family.diseases,name:"
+msgid "Family Diseases"
+msgstr "Enfermedades Familiares"
+
+msgctxt "model:gnuhealth.patient.genetic.risk,name:"
+msgid "Patient Genetic Risks"
+msgstr "Riesgos Genéticos del Paciente"
+
+msgctxt "model:ir.action,name:gnuhealth_action_disease_gene"
+msgid "Disease Genes"
+msgstr "Genes patológicos"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_disease_genes"
+msgid "Disease Genes"
+msgstr "Genes patológicos"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_genetics"
+msgid "Genetics"
+msgstr "Genética"
+
+msgctxt "model:res.group,name:group_health_genetics_admin"
+msgid "Health Genetics Administration"
+msgstr "Administración de Genética de Health"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "dominant"
+msgstr "dominante"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "recessive"
+msgstr "recesivo"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Aunt"
+msgstr "Tía"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Brother"
+msgstr "Hermano"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Cousin"
+msgstr "Primo/a"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Father"
+msgstr "Padre"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandfather"
+msgstr "Abuelo"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandmother"
+msgstr "Abuela"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Mother"
+msgstr "Madre"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Nephew"
+msgstr "Sobrino"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Niece"
+msgstr "Sobrina"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Sister"
+msgstr "Hermana"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Uncle"
+msgstr "Tío"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal"
+msgstr "Materno"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Paternal"
+msgstr "Paterno"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Sibling"
+msgstr "Hermano/a"
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Disease Genes"
+msgstr "Genes patológicos"
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Medical Genetic Risks"
+msgstr "Riesgos Genéticos Médicos"
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Genetic Family History"
+msgstr "Historial Genético Familiar"
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Patient Family History"
+msgstr "Historial genético familiar del paciente"
+
+msgctxt "view:gnuhealth.patient.genetic.risk:"
+msgid "Patient Genetic Risks"
+msgstr "Riesgos Genéticos del Paciente"
+
+msgctxt "view:gnuhealth.patient:"
+msgid "Genetics"
+msgstr "Genética"
diff --git a/locale/fr_FR.po b/locale/fr_FR.po
new file mode 100644
index 0000000..dbe271b
--- /dev/null
+++ b/locale/fr_FR.po
@@ -0,0 +1,295 @@
+#
+# Translators:
+# Eric Vernichon <eric at vernichon.fr>, 2011-2012
+# gestionRessources <klinik_mailinglist at gestion-ressources.com>, 2011
+msgid ""
+msgstr ""
+"Project-Id-Version: GNU Health\n"
+"Report-Msgid-Bugs-To: https://savannah.gnu.org/bugs/?group=health\n"
+"POT-Creation-Date: 2015-01-27 11:17+0000\n"
+"PO-Revision-Date: 2015-01-13 14:54+0000\n"
+"Last-Translator: Bruno Villasanti <bvillasanti at thymbra.com>\n"
+"Language-Team: French (France) (http://www.transifex.com/projects/p/GNU_Health/language/fr_FR/)\n"
+"MIME-Version: 1.0\n"
+"Content-Type: text/plain; charset=UTF-8\n"
+"Content-Transfer-Encoding: 8bit\n"
+"Language: fr_FR\n"
+"Plural-Forms: nplurals=2; plural=(n > 1);\n"
+
+msgctxt "error:gnuhealth.disease.gene:"
+msgid "The Official Symbol name must be unique !"
+msgstr ""
+
+msgctxt "field:gnuhealth.disease.gene,chromosome:"
+msgid "Affected Chromosome"
+msgstr "Chromosome Affecté"
+
+msgctxt "field:gnuhealth.disease.gene,create_date:"
+msgid "Create Date"
+msgstr "Date de création"
+
+msgctxt "field:gnuhealth.disease.gene,create_uid:"
+msgid "Create User"
+msgstr "Créé par"
+
+msgctxt "field:gnuhealth.disease.gene,dominance:"
+msgid "Dominance"
+msgstr "Dominance"
+
+msgctxt "field:gnuhealth.disease.gene,gene_id:"
+msgid "Gene ID"
+msgstr "ID Gène"
+
+msgctxt "field:gnuhealth.disease.gene,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.disease.gene,info:"
+msgid "Information"
+msgstr "Information"
+
+msgctxt "field:gnuhealth.disease.gene,location:"
+msgid "Location"
+msgstr "Emplacement"
+
+msgctxt "field:gnuhealth.disease.gene,long_name:"
+msgid "Official Long Name"
+msgstr "Nom long officiel"
+
+msgctxt "field:gnuhealth.disease.gene,name:"
+msgid "Official Symbol"
+msgstr "Symbole Officiel"
+
+msgctxt "field:gnuhealth.disease.gene,rec_name:"
+msgid "Name"
+msgstr "Nom"
+
+msgctxt "field:gnuhealth.disease.gene,write_date:"
+msgid "Write Date"
+msgstr "Date de modification"
+
+msgctxt "field:gnuhealth.disease.gene,write_uid:"
+msgid "Write User"
+msgstr "Modifié par"
+
+msgctxt "field:gnuhealth.patient,family_history:"
+msgid "Family History"
+msgstr "Historique de la famille"
+
+msgctxt "field:gnuhealth.patient,genetic_risks:"
+msgid "Genetic Risks"
+msgstr "Risques Génétiques"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_date:"
+msgid "Create Date"
+msgstr "Date de création"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_uid:"
+msgid "Create User"
+msgstr "Créé par"
+
+msgctxt "field:gnuhealth.patient.family.diseases,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.family.diseases,name:"
+msgid "Disease"
+msgstr "Maladie"
+
+msgctxt "field:gnuhealth.patient.family.diseases,patient:"
+msgid "Patient"
+msgstr "Patient"
+
+msgctxt "field:gnuhealth.patient.family.diseases,rec_name:"
+msgid "Name"
+msgstr "Nom"
+
+msgctxt "field:gnuhealth.patient.family.diseases,relative:"
+msgid "Relative"
+msgstr "Relatif"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_date:"
+msgid "Write Date"
+msgstr "Date de modification"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_uid:"
+msgid "Write User"
+msgstr "Modifié par"
+
+msgctxt "field:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal or Paternal"
+msgstr "Maternel ou paternel"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_date:"
+msgid "Create Date"
+msgstr "Date de création"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_uid:"
+msgid "Create User"
+msgstr "Créé par"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,disease_gene:"
+msgid "Disease Gene"
+msgstr "Gène de la maladie"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,notes:"
+msgid "Notes"
+msgstr "Notes"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,patient:"
+msgid "Patient"
+msgstr "Patient"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,rec_name:"
+msgid "Name"
+msgstr "Nom"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_date:"
+msgid "Write Date"
+msgstr "Date de modification"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_uid:"
+msgid "Write User"
+msgstr "Modifié par"
+
+msgctxt "help:gnuhealth.disease.gene,chromosome:"
+msgid "Name of the affected chromosome"
+msgstr "Nom du chromosome affectés"
+
+msgctxt "help:gnuhealth.disease.gene,gene_id:"
+msgid "default code from NCBI Entrez database."
+msgstr "code par défaut de la base de données NCBI."
+
+msgctxt "help:gnuhealth.disease.gene,info:"
+msgid "Extra Information"
+msgstr "Infos supplémentaires"
+
+msgctxt "help:gnuhealth.disease.gene,location:"
+msgid "Locus of the chromosome"
+msgstr "Locus du chromosome"
+
+msgctxt "help:gnuhealth.patient.family.diseases,relative:"
+msgid ""
+"First degree = siblings, mother and father; second degree = Uncles, nephews "
+"and Nieces; third degree = Grandparents and cousins"
+msgstr "Premier degré = frères et sœurs, mère et père; second degré = oncles, neveux et nièces; troisième degré = grands-parents et cousins"
+
+msgctxt "model:gnuhealth.disease.gene,name:"
+msgid "Disease Genes"
+msgstr "Gènes de la maladie"
+
+msgctxt "model:gnuhealth.patient.family.diseases,name:"
+msgid "Family Diseases"
+msgstr "Maladies de famille"
+
+msgctxt "model:gnuhealth.patient.genetic.risk,name:"
+msgid "Patient Genetic Risks"
+msgstr "Risques génétiques du patient"
+
+msgctxt "model:ir.action,name:gnuhealth_action_disease_gene"
+msgid "Disease Genes"
+msgstr "Gènes de la maladie"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_disease_genes"
+msgid "Disease Genes"
+msgstr "Gènes de la maladie"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_genetics"
+msgid "Genetics"
+msgstr "Génétique"
+
+msgctxt "model:res.group,name:group_health_genetics_admin"
+msgid "Health Genetics Administration"
+msgstr "Administration Génétique"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "dominant"
+msgstr "dominant"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "recessive"
+msgstr "recessif"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Aunt"
+msgstr "Tante"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Brother"
+msgstr "Frère"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Cousin"
+msgstr "Cousin"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Father"
+msgstr "Père"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandfather"
+msgstr "Grand-père"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandmother"
+msgstr "Grand-mère"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Mother"
+msgstr "Mère"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Nephew"
+msgstr "Neveu"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Niece"
+msgstr "Nièce"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Sister"
+msgstr "Sœur"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Uncle"
+msgstr "Oncle"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal"
+msgstr "Maternelle"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Paternal"
+msgstr "Paternel"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Sibling"
+msgstr ""
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Disease Genes"
+msgstr "Gènes de la maladie"
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Medical Genetic Risks"
+msgstr "Risque de maladie génétique"
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Genetic Family History"
+msgstr ""
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Patient Family History"
+msgstr ""
+
+msgctxt "view:gnuhealth.patient.genetic.risk:"
+msgid "Patient Genetic Risks"
+msgstr "Risques Génétiques du Patient"
+
+msgctxt "view:gnuhealth.patient:"
+msgid "Genetics"
+msgstr "Génétique"
diff --git a/locale/it_IT.po b/locale/it_IT.po
new file mode 100644
index 0000000..fc48406
--- /dev/null
+++ b/locale/it_IT.po
@@ -0,0 +1,295 @@
+#
+# Translators:
+# Selene <scordara at thymbra.com>, 2011, 2012
+# Selene <scordara at thymbra.com>, 2011-2012
+msgid ""
+msgstr ""
+"Project-Id-Version: GNU Health\n"
+"Report-Msgid-Bugs-To: https://savannah.gnu.org/bugs/?group=health\n"
+"POT-Creation-Date: 2015-01-27 11:17+0000\n"
+"PO-Revision-Date: 2015-01-13 14:54+0000\n"
+"Last-Translator: Teodoro Santoni <asbrasbra at gmail.com>\n"
+"Language-Team: Italian (http://www.transifex.com/projects/p/GNU_Health/language/it/)\n"
+"MIME-Version: 1.0\n"
+"Content-Type: text/plain; charset=UTF-8\n"
+"Content-Transfer-Encoding: 8bit\n"
+"Language: it\n"
+"Plural-Forms: nplurals=2; plural=(n != 1);\n"
+
+msgctxt "error:gnuhealth.disease.gene:"
+msgid "The Official Symbol name must be unique !"
+msgstr "Il nome del Simbolo Ufficiale dev'essere univoco !"
+
+msgctxt "field:gnuhealth.disease.gene,chromosome:"
+msgid "Affected Chromosome"
+msgstr "Cromosoma affetto"
+
+msgctxt "field:gnuhealth.disease.gene,create_date:"
+msgid "Create Date"
+msgstr "Creare Data"
+
+msgctxt "field:gnuhealth.disease.gene,create_uid:"
+msgid "Create User"
+msgstr "Creare utente"
+
+msgctxt "field:gnuhealth.disease.gene,dominance:"
+msgid "Dominance"
+msgstr "dominante"
+
+msgctxt "field:gnuhealth.disease.gene,gene_id:"
+msgid "Gene ID"
+msgstr "Identificazione Gene"
+
+msgctxt "field:gnuhealth.disease.gene,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.disease.gene,info:"
+msgid "Information"
+msgstr "Informazioni"
+
+msgctxt "field:gnuhealth.disease.gene,location:"
+msgid "Location"
+msgstr "Posizione"
+
+msgctxt "field:gnuhealth.disease.gene,long_name:"
+msgid "Official Long Name"
+msgstr "Nome ufficiale completo"
+
+msgctxt "field:gnuhealth.disease.gene,name:"
+msgid "Official Symbol"
+msgstr "Simbolo Ufficiale"
+
+msgctxt "field:gnuhealth.disease.gene,rec_name:"
+msgid "Name"
+msgstr "Nome"
+
+msgctxt "field:gnuhealth.disease.gene,write_date:"
+msgid "Write Date"
+msgstr "Scrivere Data"
+
+msgctxt "field:gnuhealth.disease.gene,write_uid:"
+msgid "Write User"
+msgstr "Scrivere nome Utente"
+
+msgctxt "field:gnuhealth.patient,family_history:"
+msgid "Family History"
+msgstr "Storia familiare"
+
+msgctxt "field:gnuhealth.patient,genetic_risks:"
+msgid "Genetic Risks"
+msgstr "Rischi genetici"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_date:"
+msgid "Create Date"
+msgstr "Creare Data"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_uid:"
+msgid "Create User"
+msgstr "Creare utente"
+
+msgctxt "field:gnuhealth.patient.family.diseases,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.family.diseases,name:"
+msgid "Disease"
+msgstr "Malattia"
+
+msgctxt "field:gnuhealth.patient.family.diseases,patient:"
+msgid "Patient"
+msgstr "Paziente"
+
+msgctxt "field:gnuhealth.patient.family.diseases,rec_name:"
+msgid "Name"
+msgstr "Nome"
+
+msgctxt "field:gnuhealth.patient.family.diseases,relative:"
+msgid "Relative"
+msgstr "Parente"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_date:"
+msgid "Write Date"
+msgstr "Scrivere Data"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_uid:"
+msgid "Write User"
+msgstr "Scrivere nome Utente"
+
+msgctxt "field:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal or Paternal"
+msgstr "Materno o Paterno"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_date:"
+msgid "Create Date"
+msgstr "Creare Data"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_uid:"
+msgid "Create User"
+msgstr "Creare Utente"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,disease_gene:"
+msgid "Disease Gene"
+msgstr "Gene patologico"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,notes:"
+msgid "Notes"
+msgstr "Note"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,patient:"
+msgid "Patient"
+msgstr "paziente"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,rec_name:"
+msgid "Name"
+msgstr "Nome"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_date:"
+msgid "Write Date"
+msgstr "Scrivere Data"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_uid:"
+msgid "Write User"
+msgstr "Scrivere Nome Utente"
+
+msgctxt "help:gnuhealth.disease.gene,chromosome:"
+msgid "Name of the affected chromosome"
+msgstr "Nome del cromosoma affetto"
+
+msgctxt "help:gnuhealth.disease.gene,gene_id:"
+msgid "default code from NCBI Entrez database."
+msgstr "codice predefinito dal database NCBI Entrez"
+
+msgctxt "help:gnuhealth.disease.gene,info:"
+msgid "Extra Information"
+msgstr "Informazioni Extra"
+
+msgctxt "help:gnuhealth.disease.gene,location:"
+msgid "Locus of the chromosome"
+msgstr "Locus del cromosoma"
+
+msgctxt "help:gnuhealth.patient.family.diseases,relative:"
+msgid ""
+"First degree = siblings, mother and father; second degree = Uncles, nephews "
+"and Nieces; third degree = Grandparents and cousins"
+msgstr "Primo grado=fratelli, madre e padre; secondo grado=zii e nipoti; terzo grado=nonni e cugini"
+
+msgctxt "model:gnuhealth.disease.gene,name:"
+msgid "Disease Genes"
+msgstr "Geni Malattia"
+
+msgctxt "model:gnuhealth.patient.family.diseases,name:"
+msgid "Family Diseases"
+msgstr "Malattie Familiari"
+
+msgctxt "model:gnuhealth.patient.genetic.risk,name:"
+msgid "Patient Genetic Risks"
+msgstr "Rischi Genetici del Paziente"
+
+msgctxt "model:ir.action,name:gnuhealth_action_disease_gene"
+msgid "Disease Genes"
+msgstr "Geni Patologici"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_disease_genes"
+msgid "Disease Genes"
+msgstr "Geni Patologici"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_genetics"
+msgid "Genetics"
+msgstr "Genetica"
+
+msgctxt "model:res.group,name:group_health_genetics_admin"
+msgid "Health Genetics Administration"
+msgstr "Amministrazione Genetica Health"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "dominant"
+msgstr "dominante"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "recessive"
+msgstr "recessivo"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Aunt"
+msgstr "Zia"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Brother"
+msgstr "Fratello"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Cousin"
+msgstr "Cugino"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Father"
+msgstr "Padre"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandfather"
+msgstr "Nonno"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandmother"
+msgstr "Nonna"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Mother"
+msgstr "Madre"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Nephew"
+msgstr "Nipote"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Niece"
+msgstr "Nipote"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Sister"
+msgstr "Sorella"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Uncle"
+msgstr "Zio"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal"
+msgstr "Materno"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Paternal"
+msgstr "Paterno"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Sibling"
+msgstr ""
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Disease Genes"
+msgstr "Geni Malattia"
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Medical Genetic Risks"
+msgstr "Rischi Genetici Medici"
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Genetic Family History"
+msgstr "Storico Genetica Familiare"
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Patient Family History"
+msgstr "Storico Familiare del Paziente"
+
+msgctxt "view:gnuhealth.patient.genetic.risk:"
+msgid "Patient Genetic Risks"
+msgstr "Rischi Genetici del Paziente"
+
+msgctxt "view:gnuhealth.patient:"
+msgid "Genetics"
+msgstr "Genetica"
diff --git a/locale/ja_JP.po b/locale/ja_JP.po
new file mode 100644
index 0000000..ad14045
--- /dev/null
+++ b/locale/ja_JP.po
@@ -0,0 +1,299 @@
+#
+# Translators:
+# Kentaro Hatori <hatori at hatochan.dyndns.org>, 2014
+# nyokohama <nyokohama at gmail.com>, 2014
+# Shigeomi Shibata, 2014
+# Shinji KOBAYASHI <skoba at moss.gr.jp>, 2014
+# Yoshida Shunsuke <koedoyoshida at gmail.com>, 2014
+# 池田 拓也 <keda.kuya.rc113 at gmail.com>, 2014
+msgid ""
+msgstr ""
+"Project-Id-Version: GNU Health\n"
+"Report-Msgid-Bugs-To: https://savannah.gnu.org/bugs/?group=health\n"
+"POT-Creation-Date: 2015-01-27 11:17+0000\n"
+"PO-Revision-Date: 2015-01-20 21:31+0000\n"
+"Last-Translator: Shigeomi Shibata\n"
+"Language-Team: Japanese (http://www.transifex.com/projects/p/GNU_Health/language/ja/)\n"
+"MIME-Version: 1.0\n"
+"Content-Type: text/plain; charset=UTF-8\n"
+"Content-Transfer-Encoding: 8bit\n"
+"Language: ja\n"
+"Plural-Forms: nplurals=1; plural=0;\n"
+
+msgctxt "error:gnuhealth.disease.gene:"
+msgid "The Official Symbol name must be unique !"
+msgstr "公式シンボルは重複禁止です !"
+
+msgctxt "field:gnuhealth.disease.gene,chromosome:"
+msgid "Affected Chromosome"
+msgstr "保因染色体"
+
+msgctxt "field:gnuhealth.disease.gene,create_date:"
+msgid "Create Date"
+msgstr "作成日"
+
+msgctxt "field:gnuhealth.disease.gene,create_uid:"
+msgid "Create User"
+msgstr "作成者"
+
+msgctxt "field:gnuhealth.disease.gene,dominance:"
+msgid "Dominance"
+msgstr "優生"
+
+msgctxt "field:gnuhealth.disease.gene,gene_id:"
+msgid "Gene ID"
+msgstr "遺伝子ID"
+
+msgctxt "field:gnuhealth.disease.gene,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.disease.gene,info:"
+msgid "Information"
+msgstr "情報"
+
+msgctxt "field:gnuhealth.disease.gene,location:"
+msgid "Location"
+msgstr "場所"
+
+msgctxt "field:gnuhealth.disease.gene,long_name:"
+msgid "Official Long Name"
+msgstr "公式ロングネーム"
+
+msgctxt "field:gnuhealth.disease.gene,name:"
+msgid "Official Symbol"
+msgstr "公式シンボル"
+
+msgctxt "field:gnuhealth.disease.gene,rec_name:"
+msgid "Name"
+msgstr "名前"
+
+msgctxt "field:gnuhealth.disease.gene,write_date:"
+msgid "Write Date"
+msgstr "記載日"
+
+msgctxt "field:gnuhealth.disease.gene,write_uid:"
+msgid "Write User"
+msgstr "記載者"
+
+msgctxt "field:gnuhealth.patient,family_history:"
+msgid "Family History"
+msgstr "家族歴"
+
+msgctxt "field:gnuhealth.patient,genetic_risks:"
+msgid "Genetic Risks"
+msgstr "遺伝的リスク"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_date:"
+msgid "Create Date"
+msgstr "作成日"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_uid:"
+msgid "Create User"
+msgstr "作成者"
+
+msgctxt "field:gnuhealth.patient.family.diseases,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.family.diseases,name:"
+msgid "Disease"
+msgstr "疾患"
+
+msgctxt "field:gnuhealth.patient.family.diseases,patient:"
+msgid "Patient"
+msgstr "患者"
+
+msgctxt "field:gnuhealth.patient.family.diseases,rec_name:"
+msgid "Name"
+msgstr "名前"
+
+msgctxt "field:gnuhealth.patient.family.diseases,relative:"
+msgid "Relative"
+msgstr "近親者"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_date:"
+msgid "Write Date"
+msgstr "記載日"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_uid:"
+msgid "Write User"
+msgstr "記載者"
+
+msgctxt "field:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal or Paternal"
+msgstr "母方あるいは父方"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_date:"
+msgid "Create Date"
+msgstr "作成日"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_uid:"
+msgid "Create User"
+msgstr "作成者"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,disease_gene:"
+msgid "Disease Gene"
+msgstr "疾患遺伝子"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,notes:"
+msgid "Notes"
+msgstr "備考"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,patient:"
+msgid "Patient"
+msgstr "患者"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,rec_name:"
+msgid "Name"
+msgstr "名前"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_date:"
+msgid "Write Date"
+msgstr "記載日"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_uid:"
+msgid "Write User"
+msgstr "記載者"
+
+msgctxt "help:gnuhealth.disease.gene,chromosome:"
+msgid "Name of the affected chromosome"
+msgstr "保因染色体の名前"
+
+msgctxt "help:gnuhealth.disease.gene,gene_id:"
+msgid "default code from NCBI Entrez database."
+msgstr "NCBI Entrez DBからの既定コード"
+
+msgctxt "help:gnuhealth.disease.gene,info:"
+msgid "Extra Information"
+msgstr "特記事項"
+
+msgctxt "help:gnuhealth.disease.gene,location:"
+msgid "Locus of the chromosome"
+msgstr "染色体の遺伝子座"
+
+msgctxt "help:gnuhealth.patient.family.diseases,relative:"
+msgid ""
+"First degree = siblings, mother and father; second degree = Uncles, nephews "
+"and Nieces; third degree = Grandparents and cousins"
+msgstr "一親等 = 兄弟、母親と父親; 二親等 = おじ、おいとめい; 三親等 = 祖父母といとこ"
+
+msgctxt "model:gnuhealth.disease.gene,name:"
+msgid "Disease Genes"
+msgstr "疾患遺伝子"
+
+msgctxt "model:gnuhealth.patient.family.diseases,name:"
+msgid "Family Diseases"
+msgstr "家族性疾患"
+
+msgctxt "model:gnuhealth.patient.genetic.risk,name:"
+msgid "Patient Genetic Risks"
+msgstr "患者遺伝的リスク"
+
+msgctxt "model:ir.action,name:gnuhealth_action_disease_gene"
+msgid "Disease Genes"
+msgstr "疾患遺伝子"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_disease_genes"
+msgid "Disease Genes"
+msgstr "疾患遺伝子"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_genetics"
+msgid "Genetics"
+msgstr "遺伝子"
+
+msgctxt "model:res.group,name:group_health_genetics_admin"
+msgid "Health Genetics Administration"
+msgstr "健康遺伝子管理"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "dominant"
+msgstr "優生"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "recessive"
+msgstr "劣性"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Aunt"
+msgstr "叔母"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Brother"
+msgstr "兄弟"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Cousin"
+msgstr "いとこ"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Father"
+msgstr "父"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandfather"
+msgstr "祖父"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandmother"
+msgstr "祖母"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Mother"
+msgstr "母"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Nephew"
+msgstr "甥"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Niece"
+msgstr "姪"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Sister"
+msgstr "姉妹"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Uncle"
+msgstr "叔父"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal"
+msgstr "母方"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Paternal"
+msgstr "父方"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Sibling"
+msgstr "兄弟"
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Disease Genes"
+msgstr "疾患遺伝子"
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Medical Genetic Risks"
+msgstr "医学的な遺伝的リスク"
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Genetic Family History"
+msgstr "遺伝学的家族歴"
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Patient Family History"
+msgstr "患者家族歴"
+
+msgctxt "view:gnuhealth.patient.genetic.risk:"
+msgid "Patient Genetic Risks"
+msgstr "親の遺伝的リスク"
+
+msgctxt "view:gnuhealth.patient:"
+msgid "Genetics"
+msgstr "遺伝子"
diff --git a/locale/pt_BR.po b/locale/pt_BR.po
new file mode 100644
index 0000000..eabdb18
--- /dev/null
+++ b/locale/pt_BR.po
@@ -0,0 +1,297 @@
+#
+# Translators:
+# Daniel Linhares <danielinhares at gmail.com>, 2012
+# Rafael H L Moretti <rafael.moretti at gmail.com>, 2014
+# Roberto Vasconcelos Novaes <rvnovaes at gmail.com>, 2014
+# Sérgio Serginho <sergio.dl at hotmail.com>, 2011
+msgid ""
+msgstr ""
+"Project-Id-Version: GNU Health\n"
+"Report-Msgid-Bugs-To: https://savannah.gnu.org/bugs/?group=health\n"
+"POT-Creation-Date: 2015-01-27 11:17+0000\n"
+"PO-Revision-Date: 2015-01-13 14:54+0000\n"
+"Last-Translator: Roberto Vasconcelos Novaes <rvnovaes at gmail.com>\n"
+"Language-Team: Portuguese (Brazil) (http://www.transifex.com/projects/p/GNU_Health/language/pt_BR/)\n"
+"MIME-Version: 1.0\n"
+"Content-Type: text/plain; charset=UTF-8\n"
+"Content-Transfer-Encoding: 8bit\n"
+"Language: pt_BR\n"
+"Plural-Forms: nplurals=2; plural=(n > 1);\n"
+
+msgctxt "error:gnuhealth.disease.gene:"
+msgid "The Official Symbol name must be unique !"
+msgstr "O nome do símbolo oficial deve ser único !"
+
+msgctxt "field:gnuhealth.disease.gene,chromosome:"
+msgid "Affected Chromosome"
+msgstr "Cromossomo Alterado"
+
+msgctxt "field:gnuhealth.disease.gene,create_date:"
+msgid "Create Date"
+msgstr "Criar Data"
+
+msgctxt "field:gnuhealth.disease.gene,create_uid:"
+msgid "Create User"
+msgstr "Criar Usuário"
+
+msgctxt "field:gnuhealth.disease.gene,dominance:"
+msgid "Dominance"
+msgstr "Dominância"
+
+msgctxt "field:gnuhealth.disease.gene,gene_id:"
+msgid "Gene ID"
+msgstr "ID Gene"
+
+msgctxt "field:gnuhealth.disease.gene,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.disease.gene,info:"
+msgid "Information"
+msgstr "Informação"
+
+msgctxt "field:gnuhealth.disease.gene,location:"
+msgid "Location"
+msgstr "Localização"
+
+msgctxt "field:gnuhealth.disease.gene,long_name:"
+msgid "Official Long Name"
+msgstr "Nome Completo"
+
+msgctxt "field:gnuhealth.disease.gene,name:"
+msgid "Official Symbol"
+msgstr "Símbolo Oficial"
+
+msgctxt "field:gnuhealth.disease.gene,rec_name:"
+msgid "Name"
+msgstr "Nome"
+
+msgctxt "field:gnuhealth.disease.gene,write_date:"
+msgid "Write Date"
+msgstr "Inserir Data"
+
+msgctxt "field:gnuhealth.disease.gene,write_uid:"
+msgid "Write User"
+msgstr "Inserir Usuário"
+
+msgctxt "field:gnuhealth.patient,family_history:"
+msgid "Family History"
+msgstr "Histórico Familiar"
+
+msgctxt "field:gnuhealth.patient,genetic_risks:"
+msgid "Genetic Risks"
+msgstr "Riscos Genéticos"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_date:"
+msgid "Create Date"
+msgstr "Criar Data"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_uid:"
+msgid "Create User"
+msgstr "Criar Usuário"
+
+msgctxt "field:gnuhealth.patient.family.diseases,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.family.diseases,name:"
+msgid "Disease"
+msgstr "Doença"
+
+msgctxt "field:gnuhealth.patient.family.diseases,patient:"
+msgid "Patient"
+msgstr "Paciente"
+
+msgctxt "field:gnuhealth.patient.family.diseases,rec_name:"
+msgid "Name"
+msgstr "Nome"
+
+msgctxt "field:gnuhealth.patient.family.diseases,relative:"
+msgid "Relative"
+msgstr "Parente"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_date:"
+msgid "Write Date"
+msgstr "Inserir Data"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_uid:"
+msgid "Write User"
+msgstr "Inserir Usuário"
+
+msgctxt "field:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal or Paternal"
+msgstr "Maternal or Paternal"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_date:"
+msgid "Create Date"
+msgstr "Criar Data"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_uid:"
+msgid "Create User"
+msgstr "Criar Usuário"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,disease_gene:"
+msgid "Disease Gene"
+msgstr "Gene da Doença"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,notes:"
+msgid "Notes"
+msgstr "Notas"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,patient:"
+msgid "Patient"
+msgstr "Paciente"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,rec_name:"
+msgid "Name"
+msgstr "Nome"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_date:"
+msgid "Write Date"
+msgstr "Inserir Data"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_uid:"
+msgid "Write User"
+msgstr "Inserir Usuário"
+
+msgctxt "help:gnuhealth.disease.gene,chromosome:"
+msgid "Name of the affected chromosome"
+msgstr "Nome do cromossomo alterado"
+
+msgctxt "help:gnuhealth.disease.gene,gene_id:"
+msgid "default code from NCBI Entrez database."
+msgstr "Código padrão do banco de dados do NCBI Entrez."
+
+msgctxt "help:gnuhealth.disease.gene,info:"
+msgid "Extra Information"
+msgstr "Informação Extra"
+
+msgctxt "help:gnuhealth.disease.gene,location:"
+msgid "Locus of the chromosome"
+msgstr "Locus do cromossomo"
+
+msgctxt "help:gnuhealth.patient.family.diseases,relative:"
+msgid ""
+"First degree = siblings, mother and father; second degree = Uncles, nephews "
+"and Nieces; third degree = Grandparents and cousins"
+msgstr "Primeiro grau = irmãos e irmãs, máe e pai; segundo grau= Tios, Sobrinhos e Sobrinhas; Terceiro grau= Avô ou Avó e primos"
+
+msgctxt "model:gnuhealth.disease.gene,name:"
+msgid "Disease Genes"
+msgstr "Genes de doenças"
+
+msgctxt "model:gnuhealth.patient.family.diseases,name:"
+msgid "Family Diseases"
+msgstr "Doenças Familiares"
+
+msgctxt "model:gnuhealth.patient.genetic.risk,name:"
+msgid "Patient Genetic Risks"
+msgstr "Riscos Genéticos dos Pacientes"
+
+msgctxt "model:ir.action,name:gnuhealth_action_disease_gene"
+msgid "Disease Genes"
+msgstr "Genes de Doenças"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_disease_genes"
+msgid "Disease Genes"
+msgstr "Genes de Doenças"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_genetics"
+msgid "Genetics"
+msgstr "Genética"
+
+msgctxt "model:res.group,name:group_health_genetics_admin"
+msgid "Health Genetics Administration"
+msgstr "Administração de Saúde Genética"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "dominant"
+msgstr "Dominante"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "recessive"
+msgstr "Recessivo"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Aunt"
+msgstr "Tia"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Brother"
+msgstr "Irmão"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Cousin"
+msgstr "Primo"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Father"
+msgstr "Pai"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandfather"
+msgstr "Avô"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandmother"
+msgstr "Avó"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Mother"
+msgstr "Mãe"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Nephew"
+msgstr "Sobrinho"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Niece"
+msgstr "Sobrinha"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Sister"
+msgstr "Irmã"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Uncle"
+msgstr "Tio"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal"
+msgstr "Materno"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Paternal"
+msgstr "Paterno"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Sibling"
+msgstr "Descendente"
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Disease Genes"
+msgstr "Genes Doentes"
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Medical Genetic Risks"
+msgstr "Riscos Genéticos"
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Genetic Family History"
+msgstr "Histórico Genético Familiar"
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Patient Family History"
+msgstr "Histórico Familiar do Paciente"
+
+msgctxt "view:gnuhealth.patient.genetic.risk:"
+msgid "Patient Genetic Risks"
+msgstr "Riscos Genéticos dos Pacientes"
+
+msgctxt "view:gnuhealth.patient:"
+msgid "Genetics"
+msgstr "Genética"
diff --git a/locale/zh_CN.po b/locale/zh_CN.po
new file mode 100644
index 0000000..214de6a
--- /dev/null
+++ b/locale/zh_CN.po
@@ -0,0 +1,296 @@
+#
+# Translators:
+# hhuang <lxvsyw at qq.com>, 2012
+# casely, 2013
+# Philip Li <Horatii.Lee at gmail.com>, 2013
+msgid ""
+msgstr ""
+"Project-Id-Version: GNU Health\n"
+"Report-Msgid-Bugs-To: https://savannah.gnu.org/bugs/?group=health\n"
+"POT-Creation-Date: 2015-01-27 11:17+0000\n"
+"PO-Revision-Date: 2015-01-13 14:54+0000\n"
+"Last-Translator: Bruno Villasanti <bvillasanti at thymbra.com>\n"
+"Language-Team: Chinese (http://www.transifex.com/projects/p/GNU_Health/language/zh/)\n"
+"MIME-Version: 1.0\n"
+"Content-Type: text/plain; charset=UTF-8\n"
+"Content-Transfer-Encoding: 8bit\n"
+"Language: zh\n"
+"Plural-Forms: nplurals=1; plural=0;\n"
+
+msgctxt "error:gnuhealth.disease.gene:"
+msgid "The Official Symbol name must be unique !"
+msgstr ""
+
+msgctxt "field:gnuhealth.disease.gene,chromosome:"
+msgid "Affected Chromosome"
+msgstr "受影响的染色体"
+
+msgctxt "field:gnuhealth.disease.gene,create_date:"
+msgid "Create Date"
+msgstr "创建日期"
+
+msgctxt "field:gnuhealth.disease.gene,create_uid:"
+msgid "Create User"
+msgstr "创建用户"
+
+msgctxt "field:gnuhealth.disease.gene,dominance:"
+msgid "Dominance"
+msgstr "优势"
+
+msgctxt "field:gnuhealth.disease.gene,gene_id:"
+msgid "Gene ID"
+msgstr "基因编号"
+
+msgctxt "field:gnuhealth.disease.gene,id:"
+msgid "ID"
+msgstr "编号"
+
+msgctxt "field:gnuhealth.disease.gene,info:"
+msgid "Information"
+msgstr "信息"
+
+msgctxt "field:gnuhealth.disease.gene,location:"
+msgid "Location"
+msgstr "位置"
+
+msgctxt "field:gnuhealth.disease.gene,long_name:"
+msgid "Official Long Name"
+msgstr "官方名称"
+
+msgctxt "field:gnuhealth.disease.gene,name:"
+msgid "Official Symbol"
+msgstr "官方标志"
+
+msgctxt "field:gnuhealth.disease.gene,rec_name:"
+msgid "Name"
+msgstr "名字"
+
+msgctxt "field:gnuhealth.disease.gene,write_date:"
+msgid "Write Date"
+msgstr "请您写日期"
+
+msgctxt "field:gnuhealth.disease.gene,write_uid:"
+msgid "Write User"
+msgstr "请您写用户"
+
+msgctxt "field:gnuhealth.patient,family_history:"
+msgid "Family History"
+msgstr "家族史"
+
+msgctxt "field:gnuhealth.patient,genetic_risks:"
+msgid "Genetic Risks"
+msgstr "遗传风险"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_date:"
+msgid "Create Date"
+msgstr "创建日期"
+
+msgctxt "field:gnuhealth.patient.family.diseases,create_uid:"
+msgid "Create User"
+msgstr "创建用户"
+
+msgctxt "field:gnuhealth.patient.family.diseases,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.family.diseases,name:"
+msgid "Disease"
+msgstr "疾病"
+
+msgctxt "field:gnuhealth.patient.family.diseases,patient:"
+msgid "Patient"
+msgstr "患者"
+
+msgctxt "field:gnuhealth.patient.family.diseases,rec_name:"
+msgid "Name"
+msgstr "名字"
+
+msgctxt "field:gnuhealth.patient.family.diseases,relative:"
+msgid "Relative"
+msgstr "亲属"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_date:"
+msgid "Write Date"
+msgstr "请您写日期"
+
+msgctxt "field:gnuhealth.patient.family.diseases,write_uid:"
+msgid "Write User"
+msgstr "请您写用户"
+
+msgctxt "field:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal or Paternal"
+msgstr "母亲或父亲"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_date:"
+msgid "Create Date"
+msgstr "创建日期"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,create_uid:"
+msgid "Create User"
+msgstr "创建用户"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,disease_gene:"
+msgid "Disease Gene"
+msgstr "疾病基因"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,id:"
+msgid "ID"
+msgstr "ID"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,notes:"
+msgid "Notes"
+msgstr "注意"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,patient:"
+msgid "Patient"
+msgstr "患者"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,rec_name:"
+msgid "Name"
+msgstr "名字"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_date:"
+msgid "Write Date"
+msgstr "请您写日期"
+
+msgctxt "field:gnuhealth.patient.genetic.risk,write_uid:"
+msgid "Write User"
+msgstr "请您写用户"
+
+msgctxt "help:gnuhealth.disease.gene,chromosome:"
+msgid "Name of the affected chromosome"
+msgstr "受感染的染色体名称"
+
+msgctxt "help:gnuhealth.disease.gene,gene_id:"
+msgid "default code from NCBI Entrez database."
+msgstr "来自NCBI Entrez数据库的默认代码"
+
+msgctxt "help:gnuhealth.disease.gene,info:"
+msgid "Extra Information"
+msgstr "其它信息"
+
+msgctxt "help:gnuhealth.disease.gene,location:"
+msgid "Locus of the chromosome"
+msgstr " 染色体轨迹"
+
+msgctxt "help:gnuhealth.patient.family.diseases,relative:"
+msgid ""
+"First degree = siblings, mother and father; second degree = Uncles, nephews "
+"and Nieces; third degree = Grandparents and cousins"
+msgstr "直系亲属：父母及兄弟姐妹；\n二代亲属：伯父，侄亲；\n三代亲属：祖父母，堂兄弟"
+
+msgctxt "model:gnuhealth.disease.gene,name:"
+msgid "Disease Genes"
+msgstr "疾病基因"
+
+msgctxt "model:gnuhealth.patient.family.diseases,name:"
+msgid "Family Diseases"
+msgstr "家族遗传疾病"
+
+msgctxt "model:gnuhealth.patient.genetic.risk,name:"
+msgid "Patient Genetic Risks"
+msgstr "患者的遗传风险"
+
+msgctxt "model:ir.action,name:gnuhealth_action_disease_gene"
+msgid "Disease Genes"
+msgstr "疾病基因"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_disease_genes"
+msgid "Disease Genes"
+msgstr "疾病基因"
+
+msgctxt "model:ir.ui.menu,name:gnuhealth_conf_genetics"
+msgid "Genetics"
+msgstr "遗传学"
+
+msgctxt "model:res.group,name:group_health_genetics_admin"
+msgid "Health Genetics Administration"
+msgstr "基因卫生管理"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "dominant"
+msgstr "显性基因"
+
+msgctxt "selection:gnuhealth.disease.gene,dominance:"
+msgid "recessive"
+msgstr "隐性基因"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Aunt"
+msgstr "姨妈"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Brother"
+msgstr "兄弟"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Cousin"
+msgstr "表亲"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Father"
+msgstr "父亲"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandfather"
+msgstr "祖父"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Grandmother"
+msgstr "祖母"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Mother"
+msgstr "母亲"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Nephew"
+msgstr "侄儿"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Niece"
+msgstr "侄女"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Sister"
+msgstr "姐妹"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,relative:"
+msgid "Uncle"
+msgstr "叔叔"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Maternal"
+msgstr "母系"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Paternal"
+msgstr "父系"
+
+msgctxt "selection:gnuhealth.patient.family.diseases,xory:"
+msgid "Sibling"
+msgstr ""
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Disease Genes"
+msgstr "疾病基因"
+
+msgctxt "view:gnuhealth.disease.gene:"
+msgid "Medical Genetic Risks"
+msgstr "医学遗传风险"
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Genetic Family History"
+msgstr ""
+
+msgctxt "view:gnuhealth.patient.family.diseases:"
+msgid "Patient Family History"
+msgstr ""
+
+msgctxt "view:gnuhealth.patient.genetic.risk:"
+msgid "Patient Genetic Risks"
+msgstr "患者的遗传风险"
+
+msgctxt "view:gnuhealth.patient:"
+msgid "Genetics"
+msgstr "遗传学"
diff --git a/security/access_rights.xml b/security/access_rights.xml
new file mode 100644
index 0000000..ebc855e
--- /dev/null
+++ b/security/access_rights.xml
@@ -0,0 +1,129 @@
+<?xml version="1.0" encoding="utf-8"?>
+<!-- This file is part of GNU Health. GPL v3+ -->
+<!-- Luis Falcon . GNU Solidario -->
+<!-- Default template for permission groups -->
+
+<tryton>
+ <data>
+
+<!-- BEGIN GENETICS ADMINISTRATION GROUP ACCESS RIGHTS -->
+
+<!-- Create the Health Administration group -->
+ <record model="res.group" id="group_health_genetics_admin">
+ <field name="name">Health Genetics Administration</field>
+ </record>
+
+<!-- Assign the Group to the "admin" user -->
+
+ <record model="res.user-res.group" id="user_admin_group_health_genetics">
+ <field name="user" ref="res.user_admin"/>
+ <field name="group" ref="group_health_genetics_admin"/>
+ </record>
+
+<!-- Access to Menus -->
+ <record model="ir.ui.menu-res.group" id="menu_health_group_health_genetics_admin">
+ <field name="menu" ref="gnuhealth_conf_genetics"/>
+ <field name="group" ref="group_health_genetics_admin"/>
+ </record>
+
+
+<!-- Access rights to models for the health admin group -->
+
+ <record model="ir.model.access" id="access_health_genetics_disease_gene_admin">
+ <field name="model" search="[('model', '=', 'gnuhealth.disease.gene')]"/>
+ <field name="group" ref="group_health_genetics_admin"/>
+ <field name="perm_read" eval="True"/>
+ <field name="perm_write" eval="True"/>
+ <field name="perm_create" eval="True"/>
+ <field name="perm_delete" eval="True"/>
+ </record>
+
+ <record model="ir.model.access" id="access_health_genetics_patient_family_diseases_admin">
+ <field name="model" search="[('model', '=', 'gnuhealth.patient.family.diseases')]"/>
+ <field name="group" ref="group_health_genetics_admin"/>
+ <field name="perm_read" eval="True"/>
+ <field name="perm_write" eval="True"/>
+ <field name="perm_create" eval="True"/>
+ <field name="perm_delete" eval="True"/>
+ </record>
+
+ <record model="ir.model.access" id="access_health_genetics_patient_genetic_risk_admin">
+ <field name="model" search="[('model', '=', 'gnuhealth.patient.genetic.risk')]"/>
+ <field name="group" ref="group_health_genetics_admin"/>
+ <field name="perm_read" eval="True"/>
+ <field name="perm_write" eval="True"/>
+ <field name="perm_create" eval="True"/>
+ <field name="perm_delete" eval="True"/>
+ </record>
+
+
+<!-- END OF GENETICS ADMINISTRATION GROUP ACCESS RIGHTS -->
+
+
+<!-- BEGIN GENETICS DEFAULT ACCESS RIGHTS -->
+
+<!-- Default access rights to models -->
+
+ <record model="ir.model.access" id="access_health_genetics_disease_gene">
+ <field name="model" search="[('model', '=', 'gnuhealth.disease.gene')]"/>
+ <field name="perm_read" eval="True"/>
+ <field name="perm_write" eval="False"/>
+ <field name="perm_create" eval="False"/>
+ <field name="perm_delete" eval="False"/>
+ </record>
+
+ <record model="ir.model.access" id="access_health_genetics_patient_family_diseases">
+ <field name="model" search="[('model', '=', 'gnuhealth.patient.family.diseases')]"/>
+ <field name="perm_read" eval="False"/>
+ <field name="perm_write" eval="False"/>
+ <field name="perm_create" eval="False"/>
+ <field name="perm_delete" eval="False"/>
+ </record>
+
+ <record model="ir.model.access" id="access_health_genetics_patient_genetic_risk">
+ <field name="model" search="[('model', '=', 'gnuhealth.patient.genetic.risk')]"/>
+ <field name="perm_read" eval="False"/>
+ <field name="perm_write" eval="False"/>
+ <field name="perm_create" eval="False"/>
+ <field name="perm_delete" eval="False"/>
+ </record>
+
+
+<!-- END OF DEFAULT ACCESS RIGHTS -->
+
+
+<!-- BEGIN DOCTOR GROUP ACCESS RIGHTS -->
+
+<!-- Access rights to models for the health doctor group -->
+
+ <record model="ir.model.access" id="access_health_genetics_disease_gene_doctor">
+ <field name="model" search="[('model', '=', 'gnuhealth.disease.gene')]"/>
+ <field name="group" ref="health.group_health_doctor"/>
+ <field name="perm_read" eval="True"/>
+ <field name="perm_write" eval="False"/>
+ <field name="perm_create" eval="False"/>
+ <field name="perm_delete" eval="False"/>
+ </record>
+
+ <record model="ir.model.access" id="access_health_genetics_patient_family_diseases_doctor">
+ <field name="model" search="[('model', '=', 'gnuhealth.patient.family.diseases')]"/>
+ <field name="group" ref="health.group_health_doctor"/>
+ <field name="perm_read" eval="True"/>
+ <field name="perm_write" eval="True"/>
+ <field name="perm_create" eval="True"/>
+ <field name="perm_delete" eval="True"/>
+ </record>
+
+ <record model="ir.model.access" id="access_health_genetics_patient_genetic_risk_doctor">
+ <field name="model" search="[('model', '=', 'gnuhealth.patient.genetic.risk')]"/>
+ <field name="group" ref="health.group_health_doctor"/>
+ <field name="perm_read" eval="True"/>
+ <field name="perm_write" eval="True"/>
+ <field name="perm_create" eval="True"/>
+ <field name="perm_delete" eval="True"/>
+ </record>
+
+<!-- END OF DOCTOR GROUP ACCESS RIGHTS -->
+
+ </data>
+</tryton>
diff --git a/setup.cfg b/setup.cfg
new file mode 100644
index 0000000..861a9f5
--- /dev/null
+++ b/setup.cfg
@@ -0,0 +1,5 @@
+[egg_info]
+tag_build =
+tag_date = 0
+tag_svn_revision = 0
+
diff --git a/setup.py b/setup.py
new file mode 100644
index 0000000..fc5c7fc
--- /dev/null
+++ b/setup.py
@@ -0,0 +1,90 @@
+#!/usr/bin/env python
+# -*- coding: utf-8 -*-
+# Copyright (C) 2011 Cédric Krier
+
+# This program is free software: you can redistribute it and/or modify
+# it under the terms of the GNU General Public License as published by
+# the Free Software Foundation, either version 3 of the License, or
+# (at your option) any later version.
+
+# This program is distributed in the hope that it will be useful,
+# but WITHOUT ANY WARRANTY; without even the implied warranty of
+# MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the
+# GNU General Public License for more details.
+
+# You should have received a copy of the GNU General Public License
+# along with this program. If not, see <http://www.gnu.org/licenses/>.
+
+from setuptools import setup
+import re
+import os
+import ConfigParser
+
+def read(fname):
+ return open(os.path.join(os.path.dirname(__file__), fname)).read()
+
+config = ConfigParser.ConfigParser()
+config.readfp(open('tryton.cfg'))
+info = dict(config.items('tryton'))
+
+for key in ('depends', 'extras_depend', 'xml'):
+ if key in info:
+ info[key] = info[key].strip().splitlines()
+major_version, minor_version = 3, 4
+
+requires = []
+
+for dep in info.get('depends', []):
+ if dep.startswith('health'):
+ requires.append('trytond_%s == %s' %
+ (dep, info.get('version')))
+ elif not re.match(r'(ir|res|webdav)(\W|$)', dep):
+ requires.append('trytond_%s >= %s.%s, < %s.%s' %
+ (dep, major_version, minor_version, major_version,
+ minor_version + 1))
+requires.append('trytond >= %s.%s, < %s.%s' %
+ (major_version, minor_version, major_version, minor_version + 1))
+
+setup(name='trytond_health_genetics',
+ version=info.get('version', '0.0.1'),
+ description=info.get('description', 'GNU Health Genetics Module'),
+ author=info.get('author', 'GNU Solidario'),
+ author_email=info.get('email', 'health at gnusolidario.org'),
+ url=info.get('website', 'http://health.gnu.org/'),
+ download_url='http://ftp.gnu.org/gnu/health/',
+ package_dir={'trytond.modules.health_genetics': '.'},
+ packages=[
+ 'trytond.modules.health_genetics',
+ 'trytond.modules.health_genetics.tests',
+ ],
+ package_data={
+ 'trytond.modules.health_genetics': info.get('xml', []) \
+ + info.get('translation', []) \
+ + ['tryton.cfg', 'view/*.xml', 'doc/*.rst', 'locale/*.po',
+ 'report/*.odt', 'icons/*.svg'],
+ },
+
+ classifiers=[
+ 'Development Status :: 5 - Production/Stable',
+ 'Environment :: Plugins',
+ 'Framework :: Tryton',
+ 'Intended Audience :: Developers',
+ 'Intended Audience :: Healthcare Industry',
+ 'License :: OSI Approved :: GNU General Public License (GPL)',
+ 'Natural Language :: English',
+ 'Natural Language :: Spanish',
+ 'Operating System :: OS Independent',
+ 'Programming Language :: Python :: 2.7',
+ 'Topic :: Scientific/Engineering :: Bio-Informatics',
+ 'Topic :: Scientific/Engineering :: Medical Science Apps.',
+ ],
+ license='GPL-3',
+ install_requires=requires,
+ zip_safe=False,
+ entry_points="""
+ [trytond.modules]
+ health_genetics = trytond.modules.health_genetics
+ """,
+ test_suite='tests',
+ test_loader='trytond.test_loader:Loader',
+ )
diff --git a/tests/__init__.py b/tests/__init__.py
new file mode 100644
index 0000000..c8cb285
--- /dev/null
+++ b/tests/__init__.py
@@ -0,0 +1 @@
+from test_health_genetics import suite
diff --git a/tests/test_health_genetics.py b/tests/test_health_genetics.py
new file mode 100644
index 0000000..817066f
--- /dev/null
+++ b/tests/test_health_genetics.py
@@ -0,0 +1,41 @@
+#!/usr/bin/env python
+
+import sys, os
+DIR = os.path.abspath(os.path.normpath(os.path.join(__file__,
+ '..', '..', '..', '..', '..', 'trytond')))
+if os.path.isdir(DIR):
+ sys.path.insert(0, os.path.dirname(DIR))
+
+import unittest
+import trytond.tests.test_tryton
+from trytond.tests.test_tryton import test_view, test_depends
+
+
+class HealthGeneticsTestCase(unittest.TestCase):
+ '''
+ Test HealthGenetics module.
+ '''
+
+ def setUp(self):
+ trytond.tests.test_tryton.install_module('health_genetics')
+
+ def test0005views(self):
+ '''
+ Test views.
+ '''
+ test_view('health_genetics')
+
+ def test0006depends(self):
+ '''
+ Test depends.
+ '''
+ test_depends()
+
+def suite():
+ suite = trytond.tests.test_tryton.suite()
+ suite.addTests(unittest.TestLoader().loadTestsFromTestCase(
+ HealthGeneticsTestCase))
+ return suite
+
+if __name__ == '__main__':
+ unittest.TextTestRunner(verbosity=2).run(suite())
diff --git a/tryton.cfg b/tryton.cfg
new file mode 100644
index 0000000..a8854dc
--- /dev/null
+++ b/tryton.cfg
@@ -0,0 +1,8 @@
+[tryton]
+version=2.8.1
+depends:
+ health
+xml:
+ health_genetics_view.xml
+ data/disease_genes.xml
+ security/access_rights.xml
diff --git a/trytond_health_genetics.egg-info/PKG-INFO b/trytond_health_genetics.egg-info/PKG-INFO
new file mode 100644
index 0000000..5bcdf8b
--- /dev/null
+++ b/trytond_health_genetics.egg-info/PKG-INFO
@@ -0,0 +1,23 @@
+Metadata-Version: 1.1
+Name: trytond-health-genetics
+Version: 2.8.1
+Summary: GNU Health Genetics Module
+Home-page: http://health.gnu.org/
+Author: GNU Solidario
+Author-email: health at gnusolidario.org
+License: GPL-3
+Download-URL: http://ftp.gnu.org/gnu/health/
+Description: UNKNOWN
+Platform: UNKNOWN
+Classifier: Development Status :: 5 - Production/Stable
+Classifier: Environment :: Plugins
+Classifier: Framework :: Tryton
+Classifier: Intended Audience :: Developers
+Classifier: Intended Audience :: Healthcare Industry
+Classifier: License :: OSI Approved :: GNU General Public License (GPL)
+Classifier: Natural Language :: English
+Classifier: Natural Language :: Spanish
+Classifier: Operating System :: OS Independent
+Classifier: Programming Language :: Python :: 2.7
+Classifier: Topic :: Scientific/Engineering :: Bio-Informatics
+Classifier: Topic :: Scientific/Engineering :: Medical Science Apps.
diff --git a/trytond_health_genetics.egg-info/SOURCES.txt b/trytond_health_genetics.egg-info/SOURCES.txt
new file mode 100644
index 0000000..f596ced
--- /dev/null
+++ b/trytond_health_genetics.egg-info/SOURCES.txt
@@ -0,0 +1,55 @@
+COPYING
+MANIFEST.in
+README
+health_genetics_view.xml
+setup.py
+./__init__.py
+./health_genetics.py
+./health_genetics_view.xml
+./tryton.cfg
+./data/disease_genes.xml
+./doc/index.rst
+./icons/dna.svg
+./locale/el_GR.po
+./locale/es_ES.po
+./locale/fr_FR.po
+./locale/it_IT.po
+./locale/ja_JP.po
+./locale/pt_BR.po
+./locale/zh_CN.po
+./security/access_rights.xml
+./tests/__init__.py
+./tests/test_health_genetics.py
+./view/gnuhealth_disease_gene.xml
+./view/gnuhealth_disease_gene_tree.xml
+./view/gnuhealth_family_diseases.xml
+./view/gnuhealth_family_diseases_tree.xml
+./view/gnuhealth_genetic_risk.xml
+./view/gnuhealth_genetic_risk_tree.xml
+./view/gnuhealth_patient.xml
+data/disease_genes.xml
+doc/index.rst
+icons/README
+icons/dna.svg
+locale/el_GR.po
+locale/es_ES.po
+locale/fr_FR.po
+locale/it_IT.po
+locale/ja_JP.po
+locale/pt_BR.po
+locale/zh_CN.po
+security/access_rights.xml
+trytond_health_genetics.egg-info/PKG-INFO
+trytond_health_genetics.egg-info/SOURCES.txt
+trytond_health_genetics.egg-info/dependency_links.txt
+trytond_health_genetics.egg-info/entry_points.txt
+trytond_health_genetics.egg-info/not-zip-safe
+trytond_health_genetics.egg-info/requires.txt
+trytond_health_genetics.egg-info/top_level.txt
+view/gnuhealth_disease_gene.xml
+view/gnuhealth_disease_gene_tree.xml
+view/gnuhealth_family_diseases.xml
+view/gnuhealth_family_diseases_tree.xml
+view/gnuhealth_genetic_risk.xml
+view/gnuhealth_genetic_risk_tree.xml
+view/gnuhealth_patient.xml
\ No newline at end of file
diff --git a/trytond_health_genetics.egg-info/dependency_links.txt b/trytond_health_genetics.egg-info/dependency_links.txt
new file mode 100644
index 0000000..8b13789
--- /dev/null
+++ b/trytond_health_genetics.egg-info/dependency_links.txt
@@ -0,0 +1 @@
+
diff --git a/trytond_health_genetics.egg-info/entry_points.txt b/trytond_health_genetics.egg-info/entry_points.txt
new file mode 100644
index 0000000..87e1550
--- /dev/null
+++ b/trytond_health_genetics.egg-info/entry_points.txt
@@ -0,0 +1,4 @@
+
+ [trytond.modules]
+ health_genetics = trytond.modules.health_genetics
+
\ No newline at end of file
diff --git a/trytond_health_genetics.egg-info/not-zip-safe b/trytond_health_genetics.egg-info/not-zip-safe
new file mode 100644
index 0000000..8b13789
--- /dev/null
+++ b/trytond_health_genetics.egg-info/not-zip-safe
@@ -0,0 +1 @@
+
diff --git a/trytond_health_genetics.egg-info/requires.txt b/trytond_health_genetics.egg-info/requires.txt
new file mode 100644
index 0000000..fcccb26
--- /dev/null
+++ b/trytond_health_genetics.egg-info/requires.txt
@@ -0,0 +1,2 @@
+trytond_health == 2.8.1
+trytond >= 3.4, < 3.5
diff --git a/trytond_health_genetics.egg-info/top_level.txt b/trytond_health_genetics.egg-info/top_level.txt
new file mode 100644
index 0000000..93df119
--- /dev/null
+++ b/trytond_health_genetics.egg-info/top_level.txt
@@ -0,0 +1 @@
+trytond
diff --git a/view/gnuhealth_disease_gene.xml b/view/gnuhealth_disease_gene.xml
new file mode 100644
index 0000000..b57e4e3
--- /dev/null
+++ b/view/gnuhealth_disease_gene.xml
@@ -0,0 +1,18 @@
+<?xml version="1.0"?>
+<form string="Medical Genetic Risks">
+ <label name="name"/>
+ <field name="name"/>
+ <label name="long_name"/>
+ <field name="long_name"/>
+ <newline/>
+ <label name="chromosome"/>
+ <field name="chromosome"/>
+ <label name="dominance"/>
+ <field name="dominance"/>
+ <label name="location"/>
+ <field name="location"/>
+ <label name="gene_id"/>
+ <field name="gene_id"/>
+ <newline/>
+ <field colspan="4" name="info"/>
+</form>
diff --git a/view/gnuhealth_disease_gene_tree.xml b/view/gnuhealth_disease_gene_tree.xml
new file mode 100644
index 0000000..e5550b3
--- /dev/null
+++ b/view/gnuhealth_disease_gene_tree.xml
@@ -0,0 +1,7 @@
+<?xml version="1.0"?>
+<tree string="Disease Genes">
+ <field name="name" expand="1"/>
+ <field name="long_name" expand="1"/>
+ <field name="chromosome" expand="1"/>
+ <field name="dominance" expand="1"/>
+</tree>
diff --git a/view/gnuhealth_family_diseases.xml b/view/gnuhealth_family_diseases.xml
new file mode 100644
index 0000000..dc0ad8c
--- /dev/null
+++ b/view/gnuhealth_family_diseases.xml
@@ -0,0 +1,10 @@
+<?xml version="1.0"?>
+<form string="Patient Family History">
+ <label name="name"/>
+ <field colspan="3" name="name"/>
+ <newline/>
+ <label name="xory"/>
+ <field name="xory"/>
+ <label name="relative"/>
+ <field name="relative"/>
+</form>
diff --git a/view/gnuhealth_family_diseases_tree.xml b/view/gnuhealth_family_diseases_tree.xml
new file mode 100644
index 0000000..5a4bc22
--- /dev/null
+++ b/view/gnuhealth_family_diseases_tree.xml
@@ -0,0 +1,6 @@
+<?xml version="1.0"?>
+<tree string="Genetic Family History">
+ <field name="name" expand="1"/>
+ <field name="xory" expand="1"/>
+ <field name="relative" expand="1"/>
+</tree>
diff --git a/view/gnuhealth_genetic_risk.xml b/view/gnuhealth_genetic_risk.xml
new file mode 100644
index 0000000..6276255
--- /dev/null
+++ b/view/gnuhealth_genetic_risk.xml
@@ -0,0 +1,7 @@
+<?xml version="1.0"?>
+<form string="Patient Genetic Risks">
+ <label name="patient"/>
+ <field name="patient"/>
+ <label name="disease_gene"/>
+ <field name="disease_gene"/>
+</form>
diff --git a/view/gnuhealth_genetic_risk_tree.xml b/view/gnuhealth_genetic_risk_tree.xml
new file mode 100644
index 0000000..b0bbcd5
--- /dev/null
+++ b/view/gnuhealth_genetic_risk_tree.xml
@@ -0,0 +1,7 @@
+<?xml version="1.0"?>
+<tree string="Patient Genetic Risks">
+ <field name="patient"/>
+ <field name="disease_gene" expand="1"/>
+ <field name="notes" expand="1"/>
+
+</tree>
diff --git a/view/gnuhealth_patient.xml b/view/gnuhealth_patient.xml
new file mode 100644
index 0000000..7366d55
--- /dev/null
+++ b/view/gnuhealth_patient.xml
@@ -0,0 +1,9 @@
+<?xml version="1.0"?>
+<data>
+ <xpath expr="/form/notebook/page[@id="patient_diseases"]" position="after">
+ <page string="Genetics" id="patient_genetics">
+ <field name="genetic_risks"/>
+ <field name="family_history"/>
+ </page>
+ </xpath>
+</data>
--
tryton-modules-health-genetics
More information about the tryton-debian-vcs
mailing list