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
05605 EIEE62 encephalopathy, epileptic, early infantile, type 62 (EIEE-62) 617938 AD - - SCN3A - autosomal dominant
05604 FFEVF4 epilepsy, familial focal, with variable foci, type 4 (FFEVF-4) 617935 AD - - SCN3A - autosomal dominant
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