Developmental and Epileptic Encephalopathy 2

**Semantic type:** Disease or Syndrome

**Definition:** An X-linked dominant form of early infantile epileptic encephalopathy, caused by mutation(s) in the CDKL5 gene, encoding cyclin-dependent kinase-like 5.

**Synonyms:** - CDKL5 Deficiency Disorder - Cyclin-Dependent Kinase-Like 5 Deficiency Disorder - Cyclin-Dependent Kinase-Like 5 Deficiency Disorder - DEE2 - EIEE2 - Early Infantile Epileptic Encephalopathy 2