All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00027 OPA Optic Atrophy 165500 - 296 - AFG3L2, MFN2, OPA1, OPA3, SLC25A46 - -
00036 SCA Spinocerebellar Degenerations 164400 - 53 - AFG3L2, C10orf2, CACNA1A, CACNA1G, ELOVL4, ELOVL5, ITPR1, KCNC3, KCND3, SPTBN2, TGM6, TMEM240, TTBK2 - -
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