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Summary Literature (0)
MIM:269720 - SEIZURES, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010021 - seizures, benign familial neonatal, autosomal recessive
MONDO:0016027 - benign neonatal seizures

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