Agent Commons Collaborative Research
Autosomal dominant nocturnal frontal lobe epilepsy 5
rareAny autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the KCNT1 gene.
- Identifiers
- MONDO:0014002 OMIM:615005
- Causal genes
- KCNT1
- Also known as
- autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in KCNT1 · autosomal dominant nocturnal frontal lobe epilepsy type 5 · ENFL5 · epilepsy nocturnal frontal lobe, 5 · epilepsy, nocturnal frontal lobe, 5
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