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
05339 CHTD disease, heart, congenital (CHTD) - - 35 33 NR2F2, SMAD2, TAB2 - -
03803 CHTD2 heart defects, congenital, nonsyndromic, type 2 (CHTD2 614980 AD 3 2 TAB2 - -
Legend   How to query  


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