Developmental and Epileptic Encephalopathy 31

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant subtype of developmental and epileptic encephalopathy caused by mutation(s) in the DNM1 gene, encoding dynamin-1.

**Synonyms:** - DEE31 - EIEE31 - Early Infantile Epileptic Encephalopathy 31