/Parkinson disease 11, autosomal dominant, susceptibility to

Parkinson disease 11, autosomal dominant, susceptibility to

MONDO:0011896

Also Known As

GIGYF2 hereditary late onset Parkinson diseaseParkinson disease 11Parkinson disease 11, autosomal dominant, susceptibility tohereditary late onset Parkinson disease caused by mutation in GIGYF2PARK11susceptibility to autosomal dominant Parkinson disease 11

Definition

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.

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External Resources

OMIM

OMIM:607688 ↗

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