Monarch Disease Ontology id MONDO_0007365 (seizures, benign familial neonatal, 1) is any benign neonatal seizures in which the cause of the disease is a mutation in the KCNQ2 gene. Also known as: KCNQ2 benign neonatal seizures, benign neonatal seizures caused by mutation in KCNQ2, seizures, benign familial neonatal, type 1, seizures, benign neonatal, 1.