Developmental and Epileptic Encephalopathy 14

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant subtype of developmental and epileptic encephalopathy caused by mutation(s) in the KCNT1 gene, encoding potassium channel subfamily T member 1.

**Synonyms:** - DEE14 - EIEE14 - Epileptic Encephalopathy, Early Infantile, 14