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DOID:0111690 - familial adult myoclonic epilepsy 1
Disease Ontology Definition:A familial adult myoclonic epilepsy that has_material_basis_in a heterozygous 5-bp repeat expansion in the SAMD12 gene on chromosome 8q24.11-q24.12.
Synonyms: BAFME1, FAME1, FCMTE1, benign adult familial myoclonic epilepsy 1, familial cortical myoclonic tremor and epilepsy 1,
Xenbase Genes : samd12
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee