GTR Home > Conditions/Phenotypes > Parkinson disease 13


Any young-onset Parkinson disease in which the cause of the disease is a mutation in the HTRA2 gene. [from MONDO]

Available tests

34 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: MGCA8, OMI, PARK13, PRSS25, HTRA2
    Summary: HtrA serine peptidase 2

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