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Summary Literature (0)
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 : chrnb2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011545 - autosomal dominant nocturnal frontal lobe epilepsy 3


Other Model Organisms: Alliance, 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)