| OMIM ID |
Human Disease |
| 613163 |
Gaba-Transaminase Deficiency |
| 230200 |
Galactokinase Deficiency |
| 230300 |
Galactorrhea |
| 230350 |
Galactose Epimerase Deficiency |
| 230400 |
Galactosemia |
| 256540 |
Galactosialidosis; GSL (1 mouse model) |
| 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 |
| 612365 |
Gamma Glutamyltransferase, Plasma Level of, Quantitative Trait Locus 1 |
| 612366 |
Gamma Glutamyltransferase, Plasma Level of, Quantitative Trait Locus 2 |
| 600897 |
Gap Junction Protein, Alpha-8; GJA8 |
| 603324 |
Gap Junction Protein, Beta-3; GJB3 |
| 230740 |
GAPO Syndrome |
| 613659 |
Gastric Cancer (3 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 model) |
| 606764 |
Gastrointestinal Stromal Tumor; GIST (5 mouse models) |
| 230750 |
Gastroschisis (1 mouse model) |
| 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 (1 mouse model) |
| 231095 |
Ghosal Hematodiaphyseal Dysplasia; GHDD |
| 612917 |
Giacheti Syndrome |
| 256850 |
Giant Axonal Neuropathy 1; GAN1 (1 mouse model) |
| 610100 |
Giant Axonal Neuropathy, Autosomal Dominant |
| 137500 |
Giant Neutrophil Leukocytes |
| 137550 |
Giant Pigmented Hairy Nevus; GPHN |
| 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) |
| 187800 |
Glanzmann Thrombasthenia, Autosomal Dominant (2 mouse models) |
| 273800 |
Glanzmann Thrombasthenia; GT |
| 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 |
| 615141 |
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 (1 mouse model) |
| 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 model) |
| 137940 |
Glomerulonephritis with Sparse Hair and Telangiectases (1 mouse model) |
| 137950 |
Glomerulopathy with Fibronectin Deposits 1; GFND1 |
| 601894 |
Glomerulopathy with Fibronectin Deposits 2; GFND2 |
| 138000 |
Glomuvenous Malformations; GVM (1 mouse model) |
| 202200 |
Glucocorticoid Deficiency 1; GCCD1 (1 mouse model) |
| 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 |
| 305900 |
Glucose-6-Phosphate Dehydrogenase; G6PD (2 mouse models) |
| 138110 |
Glucose-6-Phosphate Dehydrogenase-Like; G6PDL |
| 606824 |
Glucose/Galactose Malabsorption; GGM (1 mouse model) |
| 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 model) |
| 231970 |
Gluteal Muscles, Absence of |
| 614411 |
Glycerol Quantitative Trait Locus; GLYCQTL |
| 605899 |
Glycine Encephalopathy; GCE (1 mouse model) |
| 606664 |
Glycine N-Methyltransferase Deficiency (2 mouse models) |
| 240600 |
Glycogen Storage Disease 0, Liver (1 mouse model) |
| 611556 |
Glycogen Storage Disease 0, Muscle |
| 232200 |
Glycogen Storage Disease IA (2 mouse models) |
| 232220 |
Glycogen Storage Disease IB (1 mouse model) |
| 232240 |
Glycogen Storage Disease IC |
| 232300 |
Glycogen Storage Disease II (4 mouse models) |
| 232400 |
Glycogen Storage Disease III |
| 232500 |
Glycogen Storage Disease IV (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 (1 mouse model) |
| 232700 |
Glycogen Storage Disease VI |
| 232800 |
Glycogen Storage Disease VII (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 |
| 612934 |
Glycogen Storage Disease Xiv; GSD14 |
| 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 model) |
| 138770 |
GMS Syndrome |
| 139320 |
GNAS Complex Locus; GNAS |
| 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 |
| 233270 |
GOMBO Syndrome |
| 600171 |
Gonadal Agenesis |
| 233430 |
Gonadal Dysgenesis, XY Type, with Associated Anomalies |
| 424500 |
Gonadoblastoma; GBY |
| 233450 |
Goodpasture Syndrome |
| 233500 |
Gorlin-Chaudhry-Moss Syndrome |
| 602361 |
Gracile Bone Dysplasia |
| 603358 |
Gracile Syndrome (1 mouse model) |
| 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 |
| 175700 |
Greig Cephalopolysyndactyly Syndrome; GCPS (1 mouse model) |
| 214450 |
Griscelli Syndrome, Type 1; GS1 (1 mouse model) |
| 607624 |
Griscelli Syndrome, Type 2; GS2 |
| 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 model) |
| 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 |
| 612736 |
Guanidinoacetate Methyltransferase Deficiency (1 mouse model) |
| 601138 |
Guanylate Cyclase 2E; GUCY2E |
| 139290 |
Guanylate Kinase 3; GUK3 |
| 139393 |
Guillain-Barre Syndrome, Familial; GBS (1 mouse model) |
| 601187 |
Gurrieri Syndrome |
| 306500 |
Gynecomastia, Familial |
| 258870 |
Gyrate Atrophy of Choroid and Retina; GACR (2 mouse models) |
Analysis Tools