One of several diseases associated with defects in the human gene SCN2A, one of multiple sodium channel alpha subunits in human. See human disease model report for epilepsy, SCN-alpha-related (FBhh0000289). OMIM includes this disease in the phenotypic series seizures, benign familial infantile (FBhh0000301).
[updated June 2016 by FlyBase; FBrf0222196]
[SEIZURES, BENIGN FAMILIAL INFANTILE, 3; BFIS3](https://omim.org/entry/607745)
[SODIUM VOLTAGE-GATED CHANNEL, ALPHA SUBUNIT 2; SCN2A](https://omim.org/entry/182390)