Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 27
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the GRIN2B gene.
- Identifiers
- MONDO:0014505 OMIM:616139
- Part of
- GRIN2B-related complex neurodevelopmental disorderGenetic developmental and epileptic encephalopathyInfantile spasms
- Also known as
- DEE27 · developmental and epileptic encephalopathy 27 · early infantile epileptic encephalopathy caused by mutation in GRIN2B · EIEE27 · epileptic encephalopathy, early infantile, 27
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