All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00544 - GLUT1 deficiency syndrome, type 1 606777 - - - SLC2A1 - -
00545 - GLUT1 deficiency syndrome, type 2 612126 - - - SLC2A1 - -
00435 ATS tortuosity, arterial, syndrome (ATS) 208050 - - - SLC2A10 - -
00546 DYT-9 dystonia, type 9 (DYT-9) 601042 - - - SLC2A1 - -
03749 EIG-12 epilepsy, idiopathic, generalized, susceptibility to, type 12 (EIG-12) 614847 - - - SLC2A1 - -
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
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