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
01261 CORD2 dystrophy, cone-rod, type 2 (CORD-2) 120970 AD - - CRX - -
03452 LCA7 Leber congenital amaurosis, type 7 (LCA-7) 613829 - - - CRX - -
Legend   How to query  


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