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Summary Literature (0)
OMIM: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