All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02002 - Parkinson-dementia syndrome 260540 AR - - MAPT - -
00096 FTD dementia, frontotemporal (FTD) 600274 AD 429 61 MAPT, PSEN1 - -
00414 PD Parkinson disease, susceptibility to 168600 AD;AR;Mu 76 55 ADH1C, ATXN2, GBA, MAPT, TBP - -
01505 Picks Pick disease 172700 AD 5 1 MAPT, PSEN1 - -
02340 PSNP1 ophthalmoplegia, supranuclear, progressive (PSNP-1) 601104 AD 3 2 MAPT - -
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