Monarch Disease Ontology term MONDO_0013526 (progressive myoclonic epilepsy type 6) is any progressive myoclonic epilepsy in which the cause of the disease is a mutation in the GOSR2 gene. Also known as: EPM6, GOSR2 progressive myoclonic epilepsy, GOSR2-related progressive myoclonus ataxia, North Sea progressive myoclonus epilepsy, PME type 6, epilepsy, progressive myoclonic 6, epilepsy, progressive myoclonic, type 6, progressive myoclonic epilepsy caused by mutation in GOSR2.