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Summary Literature (0)
MIM:605751 - SEIZURES, BENIGN FAMILIAL INFANTILE, 2; BFIS2

Xenbase Genes: prrt2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011593 - seizures, benign familial infantile, 2
MONDO:0017615 - benign familial infantile epilepsy

Disease Ontology (DO):
DOID:0081115 - benign familial infantile seizures 2