Parkinson disease 5, autosomal dominant, susceptibility to

MONDO:0013340

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.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Inherited disease susceptibility (1316)

Including sub-types (0) Tagged with Parkinson disease 5, autosomal dominant, susceptibility to (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.