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DOID:0060682 - autosomal dominant nocturnal frontal lobe epilepsy 1
Disease Ontology Definition:An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the CHRNA4 gene on chromosome 20q13.
Synonyms: ENFL1, nocturnal frontal lobe epilepsy 1,
Echinobase Genes :
MIM:600513 - epilepsy, nocturnal frontal lobe, 1; enfl1 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee