Developmental and Epileptic Encephalopathy 7

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant form of early infantile epileptic encephalopathy caused by mutation(s) in the KCNQ2 gene, encoding potassium voltage-gated channel subfamily KQT member 2.

**Synonyms:** - DEE7 - EIEE7 - Epileptic Encephalopathy, Early Infantile, 7