All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02683 EJA-1 epilepsy, juvenile absence, susceptibility to, type 1 (EJA-1) 607631 - 1 1 EFHC1 - -
01952 EJM epilepsy, myoclonic, juvenile (EJM) 254770 - 41 41 EFHC1 - autosomal dominant
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