Developmental and Epileptic Encephalopathy 25

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal recessive form of early infantile epileptic encephalopathy, caused by mutation(s) in the SLC13A5 gene, encoding solute carrier family 13 member 5.

**Synonyms:** - EIEE25 - Early Infantile Epileptic Encephalopathy 25 - SLC13A5 Deficiency