Developmental and Epileptic Encephalopathy 47

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant subtype of developmental and epileptic encephalopathy, caused by mutation(s) in the FGF12 gene, encoding fibroblast growth factor 12.

**Synonyms:** - DEE47 - EIEE47 - Epileptic Encephalopathy, Early Infantile, 47