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DOID:0111689 - familial adult myoclonic epilepsy
Disease Ontology Definition:An adolescence-adult electroclinical syndrome characterized by adult-onset cortical myoclonus typically first seen as tremulous finger movements and myoclonus of the extremities.
Synonyms: BAFME, FAME, FCMTE, benign adult familial myoclonic epilepsy, benign adult familial myoclonus epilepsy, familial cortical myoclonic tremor and epilepsy,
Xenbase Genes
:
tnrc6a,
adra2b,
rapgef2,
cntn2,
samd12
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee