All diseases

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06808 CMT2Y Charcot-Marie-Tooth disease, type 2Y 616687 AD - - VCP - -
03493 FTDALS6;ALS14 dementia, frontotemporal, and/or amyotrophic lateral sclerosis, type 6 (ALS14) 613954 AD - - VCP - -
00218 IBMPFD1 myopathy, inclusion body, with early-onset Paget disease and frontotemporal dementia, type 1 167320 AD 62 20 VCP - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.