All diseases

5 entries on 1 page. Showing entries 1 - 5.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00350 DFNA1 deafness, autosomal dominant, type 1 124900 AD 312 236 CEACAM16, DIAPH1, GRHL2 - -
02776 DFNA28 deafness, autosomal dominant, type 28 (DFNA-28) 608641 AD - - GRHL2 - -
04493 ECTDS dysplasia, ectodermal/short stature syndrome (ECTDS) 616029 AR - - GRHL2 - -
05413 PPCD dystrophy, corneal, posterior polymorphous (PPCD) - - 42 42 COL8A2, GRHL2, OVOL2, ZEB1 - -
06793 PPCD4 Corneal dystrophy, posterior polymorphous, 4 618031 AD - - GRHL2 - -
Legend   How to query  


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