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Summary Literature (7)
DOID:0060681 - autosomal dominant nocturnal frontal lobe epilepsy


Disease Ontology Definition:A frontal lobe epilepsy that is characterized by autosomal dominant inheritance with childhood onset of clusters of brief nocturnal motor seizures with hyperkinetic or tonic manifestations.

Synonyms: ENFL,

Xenbase Genes : chrnb2, depdc5, crh, chrna2, kcnt1, chrna4, cabp4

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


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), frontal lobe epilepsy (is_a)