Parkinson's disease Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/168600
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Genes

2 genes associated with the Parkinson's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
DNAJC13 DnaJ (Hsp40) homolog, subfamily C, member 13
GLUD2 glutamate dehydrogenase 2