|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||A synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions. (Human Disease Ontology, DOID_14330)|
|Downloads & Tools|
2 genes associated with the Parkinson's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.