| 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 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the Perry syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| DCTN1 | dynactin 1 |
