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GTR Home > Conditions/Phenotypes > Parkinson disease 22, autosomal dominant

Parkinson disease 22, autosomal dominant

Summary

Any Parkinson disease in which the cause of the disease is a mutation in the CHCHD2 gene. [from MONDO]

Available tests

8 tests are in the database for this condition.

Clinical tests (8 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: C7orf17, MIX17B, MNRR1, NS2TP, PARK22, CHCHD2
    Summary: coiled-coil-helix-coiled-coil-helix domain containing 2

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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