All diseases

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ID

Abbreviation

Name

OMIM ID

Inheritance

Individuals

Phenotypes

Associated with genes

Associated tissues

Disease features
00036 SCA Spinocerebellar Degenerations 164400 - 53 - AFG3L2, C10orf2, CACNA1A, CACNA1G, ELOVL4, ELOVL5, ITPR1, KCNC3, KCND3, SPTBN2, TGM6, TMEM240, TTBK2 - -
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