Perry syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/168605
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Genes

1 genes associated with the Perry syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
DCTN1 dynactin 1