All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00435 ATORS tortuosity, arterial, syndrome 208050 AR 13 13 SLC2A10 - -
00546 DYT9 dystonia, type 9 (DYT-9) 601042 AD - - SLC2A1 - -
03749 EIG12 epilepsy, idiopathic, generalized, susceptibility to, type 12 (EIG-12) 614847 AD - - SLC2A1 - -
00544 GLUT1DS1 GLUT1 deficiency syndrome, type 1, infantile onset, severe (GLUT1DS-1) 606777 AD;AR 9 9 SLC2A1 - -
00545 GLUT1DS2;DYT18 GLUT1 deficiency syndrome, type 2, childhood onset (GLUT1DS-2, dystonia type 18 (DYT-18)) 612126 AD 1 1 SLC2A1 - -
00139 ID intellectual disability (ID) - - 2708 2390 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 554 more - -
05216 SDCHCN cryohydrocytosis, stomatin-deficient, with neurologic defects (SDCHCN) 608885 AD - - SLC2A1 - -
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