autosomal dominant nocturnal frontal lobe epilepsy 5

Summary

DOID:0060686 - autosomal dominant nocturnal frontal lobe epilepsy 5

Disease Ontology Definition:An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the KCNT1 gene on chromosome 9q34.

Synonyms: ENFL5, nocturnal frontal lobe epilepsy 5

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

: kcnt1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014002 - autosomal dominant nocturnal frontal lobe epilepsy 5

MONDO:0014002 - autosomal dominant nocturnal frontal lobe epilepsy 5

MIM:

MIM:615005 - EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5

MIM:615005 - EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5

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)