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
02700 BFIS-3 seizures, infantile, benign, familial, type 2 (BFIS-3) 607745 - 1 1 SCN2A - -
03404 EIEE-11 encephalopathy, epileptic, early infantile, type 11 (EIEE-11) 613721 - 2 2 SCN2A - -
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