Parkinson disease 11, autosomal dominant, susceptibility to

An inherited susceptibility or predisposition to developing late onset Parkinson disease, in which the cause of the disease is a mutation in the GIGYF2 gene.

Also known as: GIGYF2 hereditary late onset Parkinson disease, Parkinson disease 11, Parkinson disease 11, autosomal dominant, susceptibility to, hereditary late onset Parkinson disease caused by mutation in GIGYF2, PARK11, susceptibility to autosomal dominant Parkinson disease 11

0 clinical trials for this condition and its sub-types, 0 tagged with Parkinson disease 11, autosomal dominant, susceptibility to itself.