Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 26
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the KCNB1 gene.
- Identifiers
- MONDO:0014477 OMIM:616056
- Causal genes
- KCNB1
- Part of
- Neonatal-onset developmental and epileptic encephalopathyUndetermined early-onset epileptic encephalopathy
- Also known as
- DEE26 · developmental and epileptic encephalopathy 26 · early infantile epileptic encephalopathy 26 · early infantile epileptic encephalopathy caused by mutation in KCNB1 · EIEE26
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