autosomal dominant nocturnal frontal lobe epilepsy

Summary

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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0020300 - autosomal dominant nocturnal frontal lobe epilepsy

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)