All diseases

1 entry on 1 page. Showing entry 1.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04347 FAME-2;FMCTE-2 epilepsy, myoclonic, familial adult, type 2 (FAME-2) 607876 - 0 0 ADRA2B, STARD7 - -
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