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
05876 RDMS dystrophy, retinal, with macular staphyloma 617547 AR - - C21orf2 - -
05877 SMDAX dysplasia, spondylometaphyseal, axial 602271 AR - - C21orf2 - -
Legend   How to query  


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