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
00115 CRMCC microangiopathy, cerebroretinal, with calcifications and cysts (CRMCC, Coats plus syndrome) 612199 AR 33 32 CTC1, OBFC1, TEN1 - -
06081 CRMCC2 Cerebroretinal microangiopathy with calcifications and cysts 2 617341 AR - - OBFC1 - -
Legend   How to query  


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