All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03928 FAME-5;FMCTE-5 epilepsy, myoclonic, adult, familial, type 5 (FAME-5, FMCTE-5) 615400 - 0 0 CNTN2 - autosomal recessive
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