Developmental and Epileptic Encephalopathy 11

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant form of early infantile epileptic encephalopathy caused by mutation(s) in the SCN2A gene, encoding sodium channel protein type 2 subunit alpha.

**Synonyms:** - DEE11 - EIEE11 - Early Infantile Epileptic Encephalopathy 11