has material basis in existence starts during autosomal dominant disease familial adult myoclonic epilepsy familial adult myoclonic epilepsy 2 disease_ontology MIM:607876 DOID:0111692 A familial adult myoclonic epilepsy characterized by onset of tremor affecting the fingers, hand, and voice in adolescence or young adulthood with somewhat later onset of rhythmic myoclonic jerks and generalized tonic-clonic seizures that has_material_basis_in a heterozygous 5-bp repeat expansion in STARD7 on chromosome 2q11.2. ADCME BAFME2 FAME2 FCMTE2 autosomal dominant cortical myoclonus and epilepsy benign adult familial myoclonic epilepsy 2 familial cortical myoclonic tremor and epilepsy 2 autosomal dominant inheritance Adult onset