All diseases

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05331 PCH hypoplasia, pontocerebellar (PCH) - AD;AR 32 32 TBC1D23 cerebellum -
05332 PCH11 hypoplasia, pontocerebellar, non-degenerative, type 11 (PCH-11) 617695 AR - - TBC1D23 - -
Legend   How to query  


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