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Human Disease Vocabulary Browser
The current vocabulary contains human disease, syndrome, and condition terms from Online Mendelian Inheritance in Man (OMIM database).

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Human Diseases/Syndromes Beginning with "G"

To see all annotations for a disease, click the disease name.

OMIM IDHuman Disease
613163 Gaba-Transaminase Deficiency
230200 Galactokinase Deficiency
230300 Galactorrhea
230350 Galactose Epimerase Deficiency
230400 Galactosemia
256540 Galactosialidosis; GSL (1 mouse models)
137040 Gallbladder, Agenesis of
600803 Gallbladder Disease 1; GBD1
609918 Gallbladder Disease 2; GBD2
609919 Gallbladder Disease 3; GBD3
611465 Gallbladder Disease 4; GBD4
606349 Gambling, Pathologic
137050 Gamma-A-Globulin, Defect in Assembly of
137192 Gamma-Aminobutyric Acid Receptor, Beta-3; GABRB3
230450 Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due to
603324 Gap Junction Protein, Beta-3; GJB3
230740 GAPO Syndrome
613659 Gastric Cancer (4 mouse models)
137215 Gastric Cancer, Hereditary Diffuse; HDGC
137241 Gastric Inhibitory Polypeptide Receptor; GIPR
137220 Gastric Juice Peptides
137245 Gastric Lymphoma, Primary
137130 Gastric Sneezing
137210 Gastric Volvulus, Intrathoracic
137280 Gastritis, Familial Giant Hypertrophic
137270 Gastrocutaneous Syndrome
109350 Gastroesophageal Reflux; GER (1 mouse models)
606764 Gastrointestinal Stromal Tumor; GIST (5 mouse models)
230750 Gastroschisis (1 mouse models)
610539 Gaucher Disease, Atypical, Due to Saposin C Deficiency
608013 Gaucher Disease, Perinatal Lethal
230800 Gaucher Disease, Type I (13 mouse models)
230900 Gaucher Disease, Type II (3 mouse models)
231000 Gaucher Disease, Type III (8 mouse models)
231005 Gaucher Disease, Type IIIC
607313 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis; HGPPS
231050 Geleophysic Dysplasia 1; GPHYSD1
614185 Geleophysic Dysplasia 2; GPHYSD2
609446 Generalized Epilepsy and Paroxysmal Dyskinesia; GEPD
604233 Generalized Epilepsy with Febrile Seizures Plus, Type 1; GEFSP1 (6 mouse models)
604403 Generalized Epilepsy with Febrile Seizures Plus, Type 2; GEFSP2
611277 Generalized Epilepsy with Febrile Seizures Plus, Type 3; GEFSP3
609800 Generalized Epilepsy with Febrile Seizures Plus, Type 4; GEFSP4
612279 Generalized Epilepsy with Febrile Seizures Plus, Type 6; GEFSP6
613863 Generalized Epilepsy with Febrile Seizures Plus, Type 7; GEFSP7
613828 Generalized Epilepsy with Febrile Seizures Plus, Type 8; GEFSP8
190100 Geniospasm 1; GSM1
231060 Genitopalatocardiac Syndrome
606170 Genitopatellar Syndrome; GTPTS
305690 Genitourinary Tract Anomalies
137360 Genochondromatosis
137370 Genu Valgum, St. Helena Familial
137400 Geographic Tongue and Fissured Tongue
231080 German Syndrome
231070 Geroderma Osteodysplasticum; GO
137440 Gerstmann-Straussler Disease; GSD (7 mouse models)
231095 Ghosal Hematodiaphyseal Dysplasia; GHDD
612917 Giacheti Syndrome
256850 Giant Axonal Neuropathy 1, Autosomal Recessive; GAN1 (1 mouse models)
610100 Giant Axonal Neuropathy 2, Autosomal Dominant; GAN2
137500 Giant Neutrophil Leukocytes
137560 Giant Platelet Syndrome with Thrombocytopenia
137575 Gigantiform Cementoma, Familial
143500 Gilbert Syndrome
137580 Gilles De La Tourette Syndrome; GTS (4 mouse models)
263800 Gitelman Syndrome (3 mouse models)
273800 Glanzmann Thrombasthenia; GT
612313 Glass Syndrome
137750 Glaucoma 1, Open Angle, A; GLC1A
606689 Glaucoma 1, Open Angle, B; GLC1B
602429 Glaucoma 1, Open Angle, D; GLC1D
603383 Glaucoma 1, Open Angle, F; GLC1F
609887 Glaucoma 1, Open Angle, G; GLC1G
611276 Glaucoma 1, Open Angle, H; GLC1H
609745 Glaucoma 1, Open Angle, I; GLC1I
608695 Glaucoma 1, Open Angle, J; GLC1J
608696 Glaucoma 1, Open Angle, K; GLC1K
610535 Glaucoma 1, Open Angle, M; GLC1M
611274 Glaucoma 1, Open Angle, N; GLC1N
613100 Glaucoma 1, Open Angle, O; GLC1O
177700 Glaucoma 1, Open Angle, P; GLC1P
601682 Glaucoma 1, Primary Open Angle, C; GLC1C
231300 Glaucoma 3, Primary Congenital, A; GLC3A (7 mouse models)
613085 Glaucoma 3, Primary Congenital, C; GLC3C
613086 Glaucoma 3, Primary Congenital, D; GLC3D
600975 Glaucoma 3, Primary Infantile, B; GLC3B
137763 Glaucoma and Sleep Apnea
606657 Glaucoma, Normal Tension, Susceptibility to (3 mouse models)
137760 Glaucoma, Primary Open Angle; POAG (2 mouse models)
600510 Glaucoma-Related Pigment Dispersion Syndrome; GPDS1 (5 mouse models)
137700 Glaucoma with Elevated Episcleral Venous Pressure
137800 Glioma Susceptibility 1; GLM1
613028 Glioma Susceptibility 2; GLM2 (3 mouse models)
613029 Glioma Susceptibility 3; GLM3
607248 Glioma Susceptibility 4; GLM4
613030 Glioma Susceptibility 5; GLM5
613031 Glioma Susceptibility 6; GLM6
613032 Glioma Susceptibility 7; GLM7
613033 Glioma Susceptibility 8; GLM8
137900 Globulin Anomaly Involving Beta (2a)-Globulin
609886 Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria (1 mouse models)
137940 Glomerulonephritis with Sparse Hair and Telangiectases (1 mouse models)
137950 Glomerulopathy with Fibronectin Deposits 1; GFND1
601894 Glomerulopathy with Fibronectin Deposits 2; GFND2
138000 Glomuvenous Malformations; GVM (1 mouse models)
202200 Glucocorticoid Deficiency 1; GCCD1 (1 mouse models)
607398 Glucocorticoid Deficiency 2; GCCD2
609197 Glucocorticoid Deficiency 3; GCCD3
614736 Glucocorticoid Deficiency 4; GCCD4
138040 Glucocorticoid Receptor; GCCR
103900 Glucocorticoid-Remediable Aldosteronism; GRA (2 mouse models)
614400 Glucocorticoid Therapy, Response To; GCTR
138070 Glucoglycinuria
138110 Glucose-6-Phosphate Dehydrogenase-Like; G6PDL
606824 Glucose/Galactose Malabsorption; GGM (1 mouse models)
606777 Glut1 Deficiency Syndrome 1; GLUT1DS1
612126 Glut1 Deficiency Syndrome 2; GLUT1DS2
138277 Glutamic Acid Decarboxylase, Brain, Membrane Form
610015 Glutamine Deficiency, Congenital
305920 Glutamyl Ribose-5-Phosphate Storage Disease
231670 Glutaric Acidemia I
231690 Glutaric Aciduria III
614164 Glutathione Peroxidase Deficiency; GPXD
138300 Glutathione Reductase; GSR
266130 Glutathione Synthetase Deficiency; GSSD
231900 Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia Due To; GSSDE
138340 Glutathione Transferase Activity Toward Trans-Stilbene Oxide
231950 Glutathionuria (1 mouse models)
231970 Gluteal Muscles, Absence of
307030 Glycerol Kinase Deficiency (1 mouse models)
605899 Glycine Encephalopathy; GCE (1 mouse models)
606664 Glycine N-Methyltransferase Deficiency (2 mouse models)
240600 Glycogen Storage Disease 0, Liver; GSD0A (1 mouse models)
611556 Glycogen Storage Disease 0, Muscle; GSD0B
232200 Glycogen Storage Disease IA; GSD1A (3 mouse models)
232220 Glycogen Storage Disease IB; GSD1B (1 mouse models)
232240 Glycogen Storage Disease IC
232300 Glycogen Storage Disease II; GSD2 (4 mouse models)
232400 Glycogen Storage Disease III; GSD3
232500 Glycogen Storage Disease IV; GSD4 (3 mouse models)
306000 Glycogen Storage Disease Ixa1; GSD9A1
261750 Glycogen Storage Disease Ixb; GSD9B
613027 Glycogen Storage Disease Ixc; GSD9C
261740 Glycogen Storage Disease of Heart, Lethal Congenital (2 mouse models)
300559 Glycogen Storage Disease, Type Ixd; GSD9D (2 mouse models)
232600 Glycogen Storage Disease V; GSD5 (1 mouse models)
232700 Glycogen Storage Disease VI; GSD6
232800 Glycogen Storage Disease VII; GSD7 (2 mouse models)
261670 Glycogen Storage Disease X; GSD10
612933 Glycogen Storage Disease XI; GSD11
611881 Glycogen Storage Disease Xii; GSD12
612932 Glycogen Storage Disease Xiii; GSD13
613507 Glycogen Storage Disease Xv; GSD15
138710 Glycoprotein, Renal
232900 Glycoprotein Storage Disease
610293 Glycosylphosphatidylinositol Deficiency
230500 Gm1-Gangliosidosis, Type I
230600 Gm1-Gangliosidosis, Type II (3 mouse models)
230650 Gm1-Gangliosidosis, Type III
272750 Gm2-Gangliosidosis, Ab Variant (1 mouse models)
138770 GMS Syndrome
166260 Gnathodiaphyseal Dysplasia; GDD
138800 Goiter, Multinodular 1, with or without Sertoli-Leydig Cell Tumors;
300273 Goiter, Multinodular 2; MNG2
606082 Goiter, Multinodular 3; MNG3
138790 Goiter, Multinodular, Cystic Renal Disease, and Digital Anomalies
609460 Goldberg-Shprintzen Megacolon Syndrome; GOSHS
233270 GOMBO Syndrome
600171 Gonadal Agenesis
233430 Gonadal Dysgenesis, XY Type, with Associated Anomalies
424500 Gonadoblastoma; GBY
233450 Goodpasture Syndrome
212840 Gordon Holmes Syndrome; GDHS (1 mouse models)
233500 Gorlin-Chaudhry-Moss Syndrome
602361 Gracile Bone Dysplasia; GCLEB
603358 Gracile Syndrome (1 mouse models)
614395 Graft-Versus-Host Disease, Susceptibility To; GVHDS
138920 Granddad Syndrome
138930 Grant Syndrome
233600 Granulocytopenia with Immunoglobulin Abnormality
306300 Granulomas, Congenital Cerebral
138990 Granulomatous Disease, Chronic, Autosomal Dominant Type
233690 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
233700 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I (4 mouse models)
233710 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II
613960 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type III
306400 Granulomatous Disease, Chronic, X-Linked; CGD (2 mouse models)
233670 Granulomatous Disease with Defect in Neutrophil Chemotaxis
139000 Granulosis Rubra Nasi
275000 Graves Disease
603388 Graves Disease, Susceptibility to, 2
300351 Graves Disease, Susceptibility to, X-Linked 1
139100 Graying of Hair, Precocious
139090 Gray Platelet Syndrome; GPS (1 mouse models)
215140 Greenberg Dysplasia; GRBGD
175700 Greig Cephalopolysyndactyly Syndrome; GCPS (1 mouse models)
214450 Griscelli Syndrome, Type 1; GS1 (1 mouse models)
607624 Griscelli Syndrome, Type 2; GS2 (1 mouse models)
609227 Griscelli Syndrome, Type 3; GS3
233800 Grouped Pigmentation of the Retina
139200 Group-Specific Component; GC
604690 Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia
233805 Growth Factors, Combined Defect of
608278 Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy
245590 Growth Hormone Insensitivity with Immunodeficiency (1 mouse models)
601351 Growth Retardation, Deafness, Femoral Epiphyseal Dysplasia, and Lacrimal Duct Obstruction
612938 Growth Retardation, Developmental Delay, Coarse Facies, and Early Death; GDFD
233810 Growth Retardation, Small and Puffy Hands and Feet, and Eczema
601138 Guanylate Cyclase 2E; GUCY2E
139290 Guanylate Kinase 3; GUK3
139393 Guillain-Barre Syndrome, Familial; GBS (2 mouse models)
601187 Gurrieri Syndrome
306500 Gynecomastia, Familial
258870 Gyrate Atrophy of Choroid and Retina; GACR (2 mouse models)

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last database update
07/15/2014
MGI 5.18
The Jackson Laboratory