Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 32
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the KCNA2 gene.
- Identifiers
- MONDO:0014607 OMIM:616366
- Causal genes
- KCNA2
- Part of
- Neonatal-onset developmental and epileptic encephalopathyUndetermined early-onset epileptic encephalopathy
- Also known as
- DEE32 · developmental and epileptic encephalopathy 32 · early infantile epileptic encephalopathy caused by mutation in KCNA2 · EIEE32 · epileptic encephalopathy, early infantile, 32
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