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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
OMIM:613163 Gaba-Transaminase Deficiency
OMIM:617557 Gabriele-De Vries Syndrome; GADEVS
OMIM:230200 Galactokinase Deficiency
OMIM:230300 Galactorrhea
OMIM:230350 Galactose Epimerase Deficiency
OMIM:230400 Galactosemia
OMIM:256540 Galactosialidosis; GSL
OMIM:137040 Gallbladder, Agenesis of
OMIM:600803 Gallbladder Disease 1; GBD1
OMIM:609918 Gallbladder Disease 2; GBD2
OMIM:609919 Gallbladder Disease 3; GBD3
OMIM:611465 Gallbladder Disease 4; GBD4
OMIM:251300 Galloway-Mowat Syndrome; GAMOS
OMIM:606349 Gambling, Pathologic
OMIM:137050 Gamma-A-Globulin, Defect in Assembly of
OMIM:230450 Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due to
OMIM:603324 Gap Junction Protein, Beta-3; GJB3
OMIM:230740 GAPO Syndrome
OMIM:613659 Gastric Cancer
OMIM:137215 Gastric Cancer, Hereditary Diffuse; HDGC
OMIM:137241 Gastric Inhibitory Polypeptide Receptor; GIPR
OMIM:137220 Gastric Juice Peptides
OMIM:137130 Gastric Sneezing
OMIM:137210 Gastric Volvulus, Intrathoracic
OMIM:137280 Gastritis, Familial Giant Hypertrophic
OMIM:137270 Gastrocutaneous Syndrome
OMIM:109350 Gastroesophageal Reflux; GER
OMIM:243150 Gastrointestinal Defects and Immunodeficiency Syndrome; GIDID
OMIM:606764 Gastrointestinal Stromal Tumor; GIST
OMIM:230750 Gastroschisis
OMIM:610539 Gaucher Disease, Atypical, Due to Saposin C Deficiency
OMIM:608013 Gaucher Disease, Perinatal Lethal
OMIM:230800 Gaucher Disease, Type I
OMIM:230900 Gaucher Disease, Type II
OMIM:231000 Gaucher Disease, Type III
OMIM:231005 Gaucher Disease, Type IIIC
OMIM:607313 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis, 1;
OMIM:617542 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis, 2;
OMIM:231050 Geleophysic Dysplasia 1; GPHYSD1
OMIM:614185 Geleophysic Dysplasia 2; GPHYSD2
OMIM:609446 Generalized Epilepsy and Paroxysmal Dyskinesia; GEPD
OMIM:604233 Generalized Epilepsy with Febrile Seizures Plus, Type 1; GEFSP1
OMIM:604403 Generalized Epilepsy with Febrile Seizures Plus, Type 2; GEFSP2
OMIM:611277 Generalized Epilepsy with Febrile Seizures Plus, Type 3; GEFSP3
OMIM:609800 Generalized Epilepsy with Febrile Seizures Plus, Type 4; GEFSP4
OMIM:612279 Generalized Epilepsy with Febrile Seizures Plus, Type 6; GEFSP6
OMIM:613863 Generalized Epilepsy with Febrile Seizures Plus, Type 7; GEFSP7
OMIM:613828 Generalized Epilepsy with Febrile Seizures Plus, Type 8; GEFSP8
OMIM:616172 Generalized Epilepsy with Febrile Seizures Plus, Type 9; GEFSP9
OMIM:190100 Geniospasm 1; GSM1
OMIM:231060 Genitopalatocardiac Syndrome
OMIM:606170 Genitopatellar Syndrome; GTPTS
OMIM:305690 Genitourinary Tract Anomalies
OMIM:137360 Genochondromatosis
OMIM:137370 Genu Valgum, St. Helena Familial
OMIM:137400 Geographic and Fissured Tongue
OMIM:231080 German Syndrome
OMIM:231070 Geroderma Osteodysplasticum; GO
OMIM:137440 Gerstmann-Straussler Disease; GSD
OMIM:231095 Ghosal Hematodiaphyseal Dysplasia; GHDD
OMIM:612917 Giacheti Syndrome
OMIM:256850 Giant Axonal Neuropathy 1, Autosomal Recessive; GAN1
OMIM:610100 Giant Axonal Neuropathy 2, Autosomal Dominant; GAN2
OMIM:137500 Giant Neutrophil Leukocytes
OMIM:137560 Giant Platelet Syndrome with Thrombocytopenia
OMIM:137575 Gigantiform Cementoma, Familial
OMIM:143500 Gilbert Syndrome
OMIM:137580 Gilles De La Tourette Syndrome; GTS
OMIM:206700 Gillespie Syndrome; GLSP
OMIM:263210 Gillessen-Kaesbach-Nishimura Syndrome; GIKANIS
OMIM:263800 Gitelman Syndrome; GTLMNS
OMIM:273800 Glanzmann Thrombasthenia; GT
OMIM:612313 Glass Syndrome; GLASS
OMIM:137750 Glaucoma 1, Open Angle, A; GLC1A
OMIM:606689 Glaucoma 1, Open Angle, B; GLC1B
OMIM:602429 Glaucoma 1, Open Angle, D; GLC1D
OMIM:603383 Glaucoma 1, Open Angle, F; GLC1F
OMIM:609887 Glaucoma 1, Open Angle, G; GLC1G
OMIM:611276 Glaucoma 1, Open Angle, H; GLC1H
OMIM:609745 Glaucoma 1, Open Angle, I; GLC1I
OMIM:608695 Glaucoma 1, Open Angle, J; GLC1J
OMIM:608696 Glaucoma 1, Open Angle, K; GLC1K
OMIM:610535 Glaucoma 1, Open Angle, M; GLC1M
OMIM:611274 Glaucoma 1, Open Angle, N; GLC1N
OMIM:613100 Glaucoma 1, Open Angle, O; GLC1O
OMIM:177700 Glaucoma 1, Open Angle, P; GLC1P
OMIM:601682 Glaucoma 1, Primary Open Angle, C; GLC1C
OMIM:231300 Glaucoma 3, Primary Congenital, A; GLC3A
OMIM:613085 Glaucoma 3, Primary Congenital, C; GLC3C
OMIM:613086 Glaucoma 3, Primary Congenital, D; GLC3D
OMIM:617272 Glaucoma 3, Primary Congenital, E; GLC3E
OMIM:600975 Glaucoma 3, Primary Infantile, B; GLC3B
OMIM:137763 Glaucoma and Sleep Apnea
OMIM:606657 Glaucoma, Normal Tension, Susceptibility to
OMIM:137760 Glaucoma, Primary Open Angle; POAG
OMIM:600510 Glaucoma-Related Pigment Dispersion Syndrome; GPDS1
OMIM:137700 Glaucoma with Elevated Episcleral Venous Pressure
OMIM:137800 Glioma Susceptibility 1; GLM1
OMIM:613028 Glioma Susceptibility 2; GLM2
OMIM:613029 Glioma Susceptibility 3; GLM3
OMIM:607248 Glioma Susceptibility 4; GLM4
OMIM:613030 Glioma Susceptibility 5; GLM5
OMIM:613031 Glioma Susceptibility 6; GLM6
OMIM:613032 Glioma Susceptibility 7; GLM7
OMIM:613033 Glioma Susceptibility 8; GLM8
OMIM:616568 Glioma Susceptibility 9; GLM9
OMIM:617260 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies; GDACCF
OMIM:137900 Globulin Anomaly Involving Beta (2a)-Globulin
OMIM:609886 Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria
OMIM:137950 Glomerulopathy with Fibronectin Deposits 1; GFND1
OMIM:601894 Glomerulopathy with Fibronectin Deposits 2; GFND2
OMIM:138000 Glomuvenous Malformations; GVM
OMIM:202200 Glucocorticoid Deficiency 1; GCCD1
OMIM:607398 Glucocorticoid Deficiency 2; GCCD2
OMIM:609197 Glucocorticoid Deficiency 3; GCCD3
OMIM:614736 Glucocorticoid Deficiency 4 with or without Mineralocorticoid Deficiency; GCCD4
OMIM:615962 Glucocorticoid Resistance, Generalized; GCCR
OMIM:614400 Glucocorticoid Therapy, Response To; GCTR
OMIM:138070 Glucoglycinuria
OMIM:138110 Glucose-6-Phosphate Dehydrogenase-Like; G6PDL
OMIM:606824 Glucose/Galactose Malabsorption; GGM
OMIM:606777 Glut1 Deficiency Syndrome 1; GLUT1DS1
OMIM:612126 Glut1 Deficiency Syndrome 2; GLUT1DS2
OMIM:229100 Glutamate Formiminotransferase Deficiency
OMIM:138277 Glutamic Acid Decarboxylase, Brain, Membrane Form
OMIM:610015 Glutamine Deficiency, Congenital
OMIM:305920 Glutamyl Ribose-5-Phosphate Storage Disease
OMIM:231670 Glutaric Acidemia I
OMIM:231690 Glutaric Aciduria III
OMIM:614164 Glutathione Peroxidase Deficiency; GPXD
OMIM:138300 Glutathione Reductase; GSR
OMIM:266130 Glutathione Synthetase Deficiency; GSSD
OMIM:231900 Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia Due To; GSSDE
OMIM:138340 Glutathione Transferase Activity Toward Trans-Stilbene Oxide
OMIM:231950 Glutathionuria
OMIM:231970 Gluteal Muscles, Absence of
OMIM:307030 Glycerol Kinase Deficiency; GKD
OMIM:605899 Glycine Encephalopathy; GCE
OMIM:617301 Glycine Encephalopathy with Normal Serum Glycine
OMIM:606664 Glycine N-Methyltransferase Deficiency
OMIM:240600 Glycogen Storage Disease 0, Liver; GSD0A
OMIM:611556 Glycogen Storage Disease 0, Muscle; GSD0B
OMIM:232200 Glycogen Storage Disease IA; GSD1A
OMIM:232220 Glycogen Storage Disease IB; GSD1B
OMIM:232240 Glycogen Storage Disease Ic; GSD1C
OMIM:232300 Glycogen Storage Disease II; GSD2
OMIM:232400 Glycogen Storage Disease III; GSD3
OMIM:232500 Glycogen Storage Disease IV; GSD4
OMIM:306000 Glycogen Storage Disease Ixa1; GSD9A1
OMIM:261750 Glycogen Storage Disease Ixb; GSD9B
OMIM:613027 Glycogen Storage Disease Ixc; GSD9C
OMIM:261740 Glycogen Storage Disease of Heart, Lethal Congenital
OMIM:300559 Glycogen Storage Disease, Type Ixd; GSD9D
OMIM:232600 Glycogen Storage Disease V; GSD5
OMIM:232700 Glycogen Storage Disease VI; GSD6
OMIM:232800 Glycogen Storage Disease VII; GSD7
OMIM:261670 Glycogen Storage Disease X; GSD10
OMIM:612933 Glycogen Storage Disease XI; GSD11
OMIM:611881 Glycogen Storage Disease Xii; GSD12
OMIM:612932 Glycogen Storage Disease Xiii; GSD13
OMIM:613507 Glycogen Storage Disease Xv; GSD15
OMIM:138710 Glycoprotein, Renal
OMIM:232900 Glycoprotein Storage Disease
OMIM:610293 Glycosylphosphatidylinositol Deficiency; GPID
OMIM:230500 Gm1-Gangliosidosis, Type I
OMIM:230600 Gm1-Gangliosidosis, Type II
OMIM:230650 Gm1-Gangliosidosis, Type III
OMIM:272750 Gm2-Gangliosidosis, Ab Variant
OMIM:138770 GMS Syndrome
OMIM:166260 Gnathodiaphyseal Dysplasia; GDD
OMIM:138800 Goiter, Multinodular 1, with or without Sertoli-Leydig Cell Tumors;
OMIM:300273 Goiter, Multinodular 2; MNG2
OMIM:606082 Goiter, Multinodular 3; MNG3
OMIM:138790 Goiter, Multinodular, Cystic Renal Disease, and Digital Anomalies
OMIM:609460 Goldberg-Shprintzen Syndrome; GOSHS
OMIM:233270 GOMBO Syndrome
OMIM:601853 Gomez-Lopez-Hernandez Syndrome; GLHS
OMIM:600171 Gonadal Agenesis
OMIM:233430 Gonadal Dysgenesis, XY Type, with Associated Anomalies
OMIM:424500 Gonadoblastoma; GBY
OMIM:233450 Goodpasture Syndrome
OMIM:212840 Gordon Holmes Syndrome; GDHS
OMIM:233500 Gorlin-Chaudhry-Moss Syndrome; GCMS
OMIM:602361 Gracile Bone Dysplasia; GCLEB
OMIM:603358 Gracile Syndrome
OMIM:614395 Graft-Versus-Host Disease, Susceptibility To; GVHDS
OMIM:138920 Granddad Syndrome
OMIM:602531 Grange Syndrome; GRNG
OMIM:138930 Grant Syndrome
OMIM:233600 Granulocytopenia with Immunoglobulin Abnormality
OMIM:306300 Granulomas, Congenital Cerebral
OMIM:138990 Granulomatous Disease, Chronic, Autosomal Dominant Type
OMIM:233690 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
OMIM:233700 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I; CDG1
OMIM:233710 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II; CDG2
OMIM:613960 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type III; CDG3
OMIM:306400 Granulomatous Disease, Chronic, X-Linked; CDGX
OMIM:233670 Granulomatous Disease with Defect in Neutrophil Chemotaxis
OMIM:139000 Granulosis Rubra Nasi
OMIM:275000 Graves Disease, Susceptibility to, 1; GRD1
OMIM:603388 Graves Disease, Susceptibility to, 2
OMIM:300351 Graves Disease, Susceptibility to, X-Linked 1
OMIM:139100 Graying of Hair, Precocious
OMIM:139090 Gray Platelet Syndrome; GPS
OMIM:215140 Greenberg Dysplasia; GRBGD
OMIM:175700 Greig Cephalopolysyndactyly Syndrome; GCPS
OMIM:214450 Griscelli Syndrome, Type 1; GS1
OMIM:607624 Griscelli Syndrome, Type 2; GS2
OMIM:609227 Griscelli Syndrome, Type 3; GS3
OMIM:233800 Grouped Pigmentation of the Retina
OMIM:604690 Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia
OMIM:233805 Growth Factors, Combined Defect of
OMIM:608278 Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy
OMIM:615925 Growth Hormone Deficiency, Isolated Partial; GHDP
OMIM:604271 Growth Hormone Insensitivity, Partial; GHIP
OMIM:245590 Growth Hormone Insensitivity with Immunodeficiency
OMIM:600946 Growth Hormone Receptor; GHR
OMIM:616489 Growth Restriction, Severe, with Distinctive Facies; GRDF
OMIM:601351 Growth Retardation, Deafness, Femoral Epiphyseal Dysplasia, and Lacrimal Duct Obstruction
OMIM:612938 Growth Retardation, Developmental Delay, and Facial Dysmorphism; GDFD
OMIM:617093 Growth Retardation, Intellectual Developmental Disorder, Hypotonia, and Hepatopathy; GRIDHH
OMIM:233810 Growth Retardation, Small and Puffy Hands and Feet, and Eczema
OMIM:601138 Guanylate Cyclase 2e, Pseudogene; GUCY2EP
OMIM:139290 Guanylate Kinase 3; GUK3
OMIM:139393 Guillain-Barre Syndrome, Familial; GBS
OMIM:601187 Gurrieri Syndrome
OMIM:306500 Gynecomastia, Familial
OMIM:258870 Gyrate Atrophy of Choroid and Retina; GACR

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last database update
08/08/2017
MGI 6.10
The Jackson Laboratory