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Summary Literature (2)
MIM:615005 - EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5

Xenbase Genes: kcnt1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014002 - autosomal dominant nocturnal frontal lobe epilepsy 5
MONDO:0020300 - autosomal dominant nocturnal frontal lobe epilepsy

Disease Ontology (DO):
DOID:0060686 - autosomal dominant nocturnal frontal lobe epilepsy 5