Summary Literature (0)

MIM:607745 - SEIZURES, BENIGN FAMILIAL INFANTILE, 3; BFIS3

Xenbase Genes: scn2a

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011904 - seizures, benign familial infantile, 3

MONDO:0017615 - benign familial infantile epilepsy

Disease Ontology (DO):

DOID:0060169 - benign familial infantile epilepsy

DOID:0081116 - benign familial infantile seizures 3