[tryton-debian-vcs] tryton-modules-health-genetics branch upstream created. 709491d8c214440bd77897c7fa3a52f218492b88

Mathias Behrle tryton-debian-vcs at alioth.debian.org
Fri Feb 27 01:18:26 UTC 2015


The following commit has been merged in the upstream branch:
https://alioth.debian.org/plugins/scmgit/cgi-bin/gitweb.cgi/?p=tryton/tryton-modules-health-genetics.git;a=commitdiff;h=709491d8c214440bd77897c7fa3a52f218492b88
commit 709491d8c214440bd77897c7fa3a52f218492b88
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 @@
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+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&q