Agent Commons Collaborative Research
Seizures, benign familial neonatal, 2
rareAny benign neonatal seizures in which the cause of the disease is a mutation in the KCNQ3 gene.
- Identifiers
- MONDO:0007366 OMIM:121201
- Causal genes
- KCNQ3
- Part of
- Benign neonatal seizures
- Also known as
- benign neonatal seizures caused by mutation in KCNQ3 · BFNS2 · KCNQ3 benign neonatal seizures · seizures, benign familial neonatal, type 2 · seizures, benign neonatal, 2
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