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
05741 OPDM myopathy, oculopharyngodistal (OPDM) - - 60 43 GIPC1, LRP12, NOTCH2NLC, RILPL1 - -
06978 OPDM4 myopathy, oculopharyngodistal, type 4 619790 AD - - RILPL1 - -
Legend   How to query  


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