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
00029 PD Parkinson Disease 168600 - 558 1 ADORA1, DNAJC13, FBXO7, LRRK2, MAPT, PARK2, PARK7, PINK1, PODXL, PRNP, PTRHD1, RIC3, SNCA, SYNJ1, VPS35 - -
00032 PSP Progressive Supranuclear Palsy 601104 - 16 - DCTN1, MAPT, PARK2 - -
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