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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: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