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seizures, benign familial neonatal, 2

Disease Summary
Associated Targets (2)
Tclin

2


Mondo Description Any benign neonatal seizures in which the cause of the disease is a mutation in the KCNQ3 gene.
Uniprot Description A disorder characterized by clusters of seizures occurring in the first days of life. Most patients have spontaneous remission by 12 months of age and show normal psychomotor development. The disorder is distinguished from benign familial infantile seizures by an earlier age at onset.
Mondo Term and Equivalent IDs
MONDO:0007366:  seizures, benign familial neonatal, 2
UMLS:C1852581: