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Summary Literature (2)
OMIM:121201 - SEIZURES, BENIGN FAMILIAL NEONATAL, 2; BFNS2


Xenbase Genes: kcnq3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007366 - seizures, benign familial neonatal, 2
MONDO:0016027 - benign neonatal seizures

Disease Ontology (DO):
DOID:14264 - benign neonatal seizures