| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/128235 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the dystonia-12 phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ATP1A3 | ATPase, Na+/K+ transporting, alpha 3 polypeptide |
