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
07189 DEE111 encephalopathy, developmental and epileptic, type 111 620504 AR - - DEPDC5 - -
02502 FFEVF1 epilepsy, familial focal, with variable foci, type 1 604364 AD 3 3 DEPDC5 - -
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