Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 21
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the NECAP1 gene.
- Identifiers
- MONDO:0014360 OMIM:615833
- Causal genes
- NECAP1
- Part of
- Neonatal-onset developmental and epileptic encephalopathyUndetermined early-onset epileptic encephalopathy
- Also known as
- DEE21 · developmental and epileptic encephalopathy 21 · early infantile epileptic encephalopathy caused by mutation in NECAP1 · EIEE21 · epileptic encephalopathy, early infantile, 21
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