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
00414 PD Parkinson disease (PD) 168600 AD;Mu 69 51 ADH1C, ATXN2, GBA, MAPT, TBP - -
01565 SCA2;ALS13 ataxia, spinocerebellar, type 2 (SCA-2, sclerosis, lateral, amyotrophic (ALS-13)) 183090 AD 0 0 ATXN2 - -
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