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
05413 PPCD dystrophy, corneal, posterior polymorphous (PPCD) - - 42 42 COL8A2, GRHL2, OVOL2, ZEB1 - -
01030 PPCD1 dystrophy, corneal, posterior polymorphous, type 1 (PPCD-1) 122000 AD - - OVOL2 - autosomal dominant
Legend   How to query  


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