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
02683 EJA1 epilepsy, juvenile absence, susceptibility to, type 1 (EJA-1) 607631 AD 1 1 EFHC1 - -
01952 EJM epilepsy, myoclonic, juvenile (EJM) 254770 AD 41 41 EFHC1 - autosomal dominant
Legend   How to query  


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