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List of all diseases starting with G
- G(M1)-GANGLIOSIDOSIS, TYPE I. PSEUDO-HURLER-DISEASE MIM=230500
- G(M1)-GANGLIOSIDOSIS, TYPE III. CHRONIC/ADULT TYPE MIM=230650
- G(M2)-GANGLIOSIDOSIS: GM2 ACTIVATOR DEFICIENCY MIM=272750
- G(M2)-GANGLIOSIDOSIS: VARIANT 0, SANDHOFF DISEASE MIM=268800
- G(M2)-GANGLIOSIDOSIS: VARIANT B, TAY-SACHS DISEASE MIM=272800
- GABA TRANSAMINASE DEFICIENCY MIM=613163
- GALACTOSEMIA (GALT-D) MIM=230400
- GALACTOSEMIA II (GALK-D) MIM=230200
- GALACTOSEMIA III (GALE-D) MIM=230350
- GALACTOSEMIA IV (GALM) MIM=137030
- GALACTOSIALIDOSIS MIM=256540
- GAMMA-AMINOBUTYRIC ACID RECEPTOR, ALPHA-6 (GABRA6) MIM=137143
- GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO MIM=230450
- GANG(M1)-GANGLIOSIDOSIS, TYPE II. LIPIDOSIS, LATE INFANTILE SYSTEMIC MIM=230600
- 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, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY MIM=610539
- GAUCHER DISEASE, PERINATAL LETHAL MIM=608013
- GILBERT SYNDROME MIM=143500
- GITELMAN SYNDROME; GTLMNS MIM=263800
- GLUCAGON DEFICIENCY MIM=138030
- GLUCAGON RECEPTOR DEFECT (GCGR) MIM=138033
- GLUCOCORTICOID DEFICIENCY 1 (GCCD1) MIM=202200
- GLUCOCORTICOID DEFICIENCY 2 (GCCD2) MIM=607398
- GLUCOCORTICOID DEFICIENCY 3 (GCCD3) MIM=609197
- GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY (GCCD4) MIM=614736
- GLUCOCORTICOID DEFICIENCY 5 (GCCD5) MIM=617825
- GLUCOCORTICOID DEFICIENCY, FAMILIAL ISOLATED. MIGEON SYNDROME MIM=202200
- GLUCOCORTICOID RESISTANCE (GCCR) MIM=615962
- GLUCOGLYCINURIA MIM=138070
- GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY MIM=300908
- GLUCOSE-GALACTOSE MALABSORPTION MIM=606824
- GLUT-1 DEFICIENCY SYNDROME (GLUT1DS1) MIM=606777
- GLUTAMATE FORMIMINOTRANSFERASE DEFICIENCY; FORMIMINOGLUTAMIC ACIDURIA (FIGLU) MIM=229100
- GLUTAMINASE DEFICIENCY WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND PROGRESSIVE ATAXIA MIM=618412
- GLUTAMINASE DEFICIENCY WITH NEONATAL EPILEPTIC ENCEPHALOPATHY (GLS) MIM=618328
- GLUTAMYL RIBOSE-5-PHOSPHATE STORAGE DISEASE MIM=305920
- GLUTARIC ACIDURIA I MIM=231670
- GLUTARIC ACIDURIA I (LOW EXCRETER) MIM=231670
- GLUTARIC ACIDURIA II (MADD, ETF) MIM=231680
- GLUTARIC ACIDURIA TYPE III MIM=231690
- GLUTATHIONE SYNTHETASE DEFICIENCY MIM=266130
- GLUTATHIONURIA MIM=231950
- GLYCEROL INTOLERANCE SYNDROM MIM=
- GLYCEROL KINASE DEFICIENCY MIM=307030
- GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE MIM=617301
- GLYCINE N-METHYLTRANSFERASE DEFICIENCY (GNMT) MIM=606664
- GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL MIM=261740
- GLYCOGEN STORAGE DISEASE TYPE 0a MIM=240600
- GLYCOGEN STORAGE DISEASE TYPE 0b MIM=611556
- GLYCOGEN STORAGE DISEASE TYPE IA MIM=232200
- GLYCOGEN STORAGE DISEASE TYPE IB MIM=232220
- GLYCOGEN STORAGE DISEASE TYPE IC MIM=232240
- GLYCOGEN STORAGE DISEASE TYPE II. ADULT ONSET MIM=232300
- GLYCOGEN STORAGE DISEASE TYPE II. INFANTILE ONSET. POMPE DISEASE MIM=232300
- GLYCOGEN STORAGE DISEASE TYPE II. JUVENILE ONSET MIM=232300
- GLYCOGEN STORAGE DISEASE TYPE IIB. DANON DISEASE MIM=300257
- GLYCOGEN STORAGE DISEASE TYPE III. FORBES DISEASE, CORI DISEASE MIM=232400
- GLYCOGEN STORAGE DISEASE TYPE IV. ANDERSEN DISEASE MIM=232500
- GLYCOGEN STORAGE DISEASE TYPE IXA (GSD9A) MIM=306000
- GLYCOGEN STORAGE DISEASE TYPE IXB (GSD9B) MIM=261750
- GLYCOGEN STORAGE DISEASE TYPE IXC (GSD9C) MIM=613027
- GLYCOGEN STORAGE DISEASE TYPE IXd (GSD9D) MIM=300559
- GLYCOGEN STORAGE DISEASE TYPE VI. HERS DISEASE MIM=232700
- GLYCOGEN STORAGE DISEASE TYPE VII. TARUI DISEASE MIM=232800
- GLYCOGEN STORAGE DISEASE TYPE VIII -> TYPE IX MIM=306000
- GLYCOGEN STORAGE DISEASE TYPE X MIM=261670
- GLYCOGEN STORAGE DISEASE TYPE XI MIM=612933
- GLYCOGEN STORAGE DISEASE TYPE XII MIM=611881
- GLYCOGEN STORAGE DISEASE TYPE XIII MIM=612932
- GLYCOGEN STORAGE DISEASE TYPE XV MIM=613507
- GLYCOGEN STORAGE DISEASE, TYPE V. McARDLE DISEASE MIM=232600
- GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY (PIGH-CDG) MIM=610293
- GOUT SUSCEPTIBILITY 1 MIM=138900
- GRACILE SYNDROME MIM=603358
- GREENBERG SKELATAL DYSPLASIA (GRBGD) MIM=215140