Seizures, benign familial neonatal, 1

MONDO:0007365

Any benign neonatal seizures in which the cause of the disease is a mutation in the KCNQ2 gene.

Also known as: myokymia, KCNQ2 benign neonatal seizures, benign neonatal seizures caused by mutation in KCNQ2, seizures, benign familial neonatal, 1, seizures, benign familial neonatal, type 1, seizures, benign neonatal, 1, BFNS1, epilepsy, benign neonatal, 1, and/or myokymia

7 clinical trials for this condition and its sub-types, 0 tagged with Seizures, benign familial neonatal, 1 itself.

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Including sub-types (7) Tagged with Seizures, benign familial neonatal, 1 (0)

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