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
00002 AD Alzheimer Disease 104300 - 634 - ABCA7, AGBL3, APOE, APP, ATP8B3, C16orf96, C3orf20, CASS4, CD2AP, CD33, CELF1, CENPJ, CFAP70, CHGB, CHMP2B, CLU, CR1, CST3, CTSF, EBLN1, 49 more - -
00036 SCA Spinocerebellar Degenerations 164400 - 53 - AFG3L2, C10orf2, CACNA1A, CACNA1G, ELOVL4, ELOVL5, ITPR1, KCNC3, KCND3, SPTBN2, TGM6, TMEM240, TTBK2 - -
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