autosomal dominant nocturnal frontal lobe epilepsy 3

Summary

DOID:0060684 - autosomal dominant nocturnal frontal lobe epilepsy 3

Disease Ontology Definition:An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the CHRNB2 gene on chromosome 1q21.

Synonyms: ENFL3, nocturnal frontal lobe epilepsy 3,

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

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011545 - autosomal dominant nocturnal frontal lobe epilepsy 3

MONDO:0011545 - autosomal dominant nocturnal frontal lobe epilepsy 3

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant nocturnal frontal lobe epilepsy (is_a)