Parkinson disease 5, autosomal dominant, susceptibility to

An inherited susceptibility or predisposition to developing young-onset Parkinson disease in which the cause of the disease is a mutation in the UCHL1 gene.

Also known as: Parkinson disease 5, autosomal dominant, susceptibility to, Parkinson disease 5, susceptibility to, UCHL1 young-onset Parkinson disease, young-onset Parkinson disease caused by mutation in UCHL1, PARK5, susceptibility to autosomal dominant Parkinson disease 5

0 clinical trials for this condition and its sub-types, 0 tagged with Parkinson disease 5, autosomal dominant, susceptibility to itself.