All diseases

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03464 - Inosine triphosphatase deficiency 613850 - - - ITPA - -
00841 EIEE encephalopathy, epileptic, early infantile (EIEE) - - 156 158 CELSR3, CPLX1, HNRNPU, ITPA, PHACTR1, RHOBTB2 - -
06502 EIEE35 Epileptic encephalopathy, early infantile, 35 616647 AR 15 1 ITPA - -
Legend   How to query  


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