Parkinson disease 13, 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 HTRA2 gene.

Also known as: HTRA2 young-onset Parkinson disease, PARK13, Parkinson disease 13, Parkinson disease 13, autosomal dominant, susceptibility to, young-onset Parkinson disease caused by mutation in HTRA2

0 clinical trials for this condition and its sub-types, 0 tagged with Parkinson disease 13, autosomal dominant, susceptibility to itself.