Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2994982015 | Rapid onset dystonia parkinsonism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2995583010 | DYT12 - dystonia 12 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 2995754010 | Rapid onset dystonia parkinsonism (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2995824011 | Dystonia 12 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2995969018 | Abrupt onset of dystonia with parkinsonism over a period of hours to days. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Rapid onset dystonia parkinsonism | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Rapid onset dystonia parkinsonism | Is a | Dystonia | true | Inferred relationship | Some | ||
| Rapid onset dystonia parkinsonism | Is a | Parkinsonism | true | Inferred relationship | Some | ||
| Rapid onset dystonia parkinsonism | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Rapid onset dystonia parkinsonism | Finding site | Basal ganglion structure (body structure) | true | Inferred relationship | Some | 1 | |
| Rapid onset dystonia parkinsonism | Interprets | Movement | true | Inferred relationship | Some | 3 | |
| Rapid onset dystonia parkinsonism | Has interpretation | Slow | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR