Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 14
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the KCNT1 gene.
- Identifiers
- MONDO:0013989 OMIM:614959
- Causal genes
- KCNT1
- Also known as
- DEE14 · developmental and epileptic encephalopathy 14 · early infantile epileptic encephalopathy caused by mutation in KCNT1 · EIEE14 · epileptic encephalopathy, early infantile, 14
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