Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 24
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the HCN1 gene.
- Identifiers
- MONDO:0014377 OMIM:615871
- Causal genes
- HCN1
- Part of
- Neonatal-onset developmental and epileptic encephalopathyUndetermined early-onset epileptic encephalopathy
- Also known as
- DEE24 · developmental and epileptic encephalopathy 24 · early infantile epileptic encephalopathy caused by mutation in HCN1 · EIEE24 · epileptic encephalopathy, early infantile, 24
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