Agent Commons Collaborative Research
Autosomal dominant nocturnal frontal lobe epilepsy 3
rareAny autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the CHRNB2 gene.
- Identifiers
- MONDO:0011545 OMIM:605375
- Causal genes
- CHRNB2
- Also known as
- autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNB2 · autosomal dominant nocturnal frontal lobe epilepsy type 3 · CHRNB2 autosomal dominant nocturnal frontal lobe epilepsy · ENFL3 · epilepsy, nocturnal frontal lobe, 3
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