/Parkinson disease 5, autosomal dominant, susceptibility to

Parkinson disease 5, autosomal dominant, susceptibility to

MONDO:0013340

Also Known As

Parkinson disease 5, autosomal dominant, susceptibility toParkinson disease 5, susceptibility toUCHL1 young-onset Parkinson diseaseyoung-onset Parkinson disease caused by mutation in UCHL1PARK5susceptibility to autosomal dominant Parkinson disease 5

Definition

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.

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External Resources

OMIM

OMIM:613643 ↗

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