All diseases

4 entries on 1 page. Showing entries 1 - 4.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00001 AD Alzheimer's disease - 0 0 APP, C9orf72, GRN, MAPT, PSEN1, PSEN2, TARDBP - -
00004 ALS amyotrophic lateral sclerosis 105400 0 0 C9orf72, FUS, TARDBP - -
00002 FTD Frontotemporal dementia - 0 0 APP, C9orf72, CHMP2B, FUS, GRN, MAPT, PSEN1, PSEN2, TARDBP, TBK1, VCP - -
00003 IBMPFD Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 167320 0 0 CHMP2B, VCP - -