| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Rapid-onset dystonia-parkinsonism (RDP) is a very rare movement disorder, characterized by the abrupt onset of parkinsonism and dystonia, often triggered by physical or psychological stress. (Orphanet Rare Disease Ontology, Orphanet_71517) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C538001 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Dystonia 12 from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| ATP1A3 | ATPase, Na+/K+ transporting, alpha 3 polypeptide | 2.88009 |
