Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 2
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the CDKL5 gene.
- Identifiers
- MONDO:0010396 OMIM:300672Orphanet:505652
- Part of
- CDKL5 disorderAtypical Rett syndromeGenetic developmental and epileptic encephalopathyInfantile spasmsMonogenic epilepsy
- Also known as
- CDKL5 early infantile epileptic encephalopathy · DEE2 · developmental and epileptic encephalopathy 2, X-linked dominant · early infantile epileptic encephalopathy caused by mutation in CDKL5 · EIEE2
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