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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,
Echinobase Genes :
MIM:615005 - epilepsy, nocturnal frontal lobe, 5; enfl5 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee