|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||Perry syndrome is a rare inherited neurodegenerative disorder characterized by rapidly progressive early-onset parkinsonism, central hypoventilation, weight loss, insomnia and depression. (Orphanet Rare Disease Ontology, Orphanet_178509)|
|Downloads & Tools|
1 genes associated with the Perry syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.