Epilepsy, Familial Adult Myoclonic, 2, also known as benign adult familial myoclonic epilepsy 2, is related to epilepsy, familial adult myoclonic, 1 and epilepsy, familial adult myoclonic, 3, and has symptoms including myoclonus An important gene associated with Epilepsy, Familial Adult Myoclonic, 2 is STARD7 (StAR Related Lipid Transfer Domain Containing 7), and among its related pathways/superpathways is 2q11.2 copy number variation syndrome. Affiliated tissues include brain, and related phenotypes are cognitive impairment and myoclonus