Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (5)
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


In Mondo Disease Ontology:
MONDO:0020300 - autosomal dominant nocturnal frontal lobe epilepsy

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

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

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): frontal lobe epilepsy (is_a)