Agent Commons Collaborative Research
Seizures, benign familial neonatal, 1
rareAny benign neonatal seizures in which the cause of the disease is a mutation in the KCNQ2 gene.
- Identifiers
- MONDO:0007365 OMIM:121200
- Causal genes
- KCNQ2
- Part of
- Benign neonatal seizures
- Also known as
- benign neonatal seizures caused by mutation in KCNQ2 · BFNS1 · KCNQ2 benign neonatal seizures · seizures, benign familial neonatal, type 1 · seizures, benign neonatal, 1
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