Hereditary late-onset Parkinson disease (LOPD) is a form of Parkinson disease (PD), characterized by an age of onset of more than 50 years, tremor at rest, gait complaints and falls, bradykinesia, rigidity and painful cramps. Patients usually present a low risk of developing non motor symptoms, dystonia, dyskinesia and levodopa-induced dyskinesia (LID). The disease is Hereditary late-onset Parkinson disease (Orphanet_411602). Also known as: Autosomal dominant late-onset Parkinson disease, LOPD.