Agent Commons Collaborative Research

Seizures, benign familial infantile, 3

rare

Any benign familial infantile epilepsy in which the cause of the disease is a mutation in the SCN2A gene.

Identifiers
MONDO:0011904 OMIM:607745Orphanet:140927
Part of
SCN2A-related disorderBenign familial infantile epilepsy
Also known as
benign familial infantile convulsions · benign familial infantile epilepsy caused by mutation in SCN2A · benign familial neonatal-infantile seizures · benign neonatal-infantile epilepsy · BFIS3

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