Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3305546018 | Congenital suprabulbar paresis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3305547010 | Congenital suprabulbar paresis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3305548017 | Worster Drought syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401303014 | Worster-Drought syndrome (WDS) is a form of cerebral palsy characterized by congenital pseudobulbar (suprabulbar) paresis manifesting as selective weakness of the lips, tongue and soft palate, dysphagia, dysphonia, drooling and jaw jerking. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401304015 | Worster-Drought syndrome (WDS) is a form of cerebral palsy characterised by congenital pseudobulbar (suprabulbar) paresis manifesting as selective weakness of the lips, tongue and soft palate, dysphagia, dysphonia, drooling and jaw jerking. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital suprabulbar paresis (disorder) | Is a | Cerebral palsy | true | Inferred relationship | Some | ||
| Congenital suprabulbar paresis (disorder) | Is a | Anomalies of cerebrum | false | Inferred relationship | Some | ||
| Congenital suprabulbar paresis (disorder) | Clinical course | Non-progressive | true | Inferred relationship | Some | 2 | |
| Congenital suprabulbar paresis (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
| Congenital suprabulbar paresis (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| Congenital suprabulbar paresis (disorder) | Finding site | Cerebrum | false | Inferred relationship | Some | 2 | |
| Congenital suprabulbar paresis (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Congenital suprabulbar paresis (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital suprabulbar paresis (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Congenital suprabulbar paresis (disorder) | Finding site | Cerebrum | true | Inferred relationship | Some | 1 | |
| Congenital suprabulbar paresis (disorder) | Is a | Congenital anomaly of cerebrum (disorder) | true | Inferred relationship | Some | ||
| Congenital suprabulbar paresis (disorder) | Interprets | Movement | true | Inferred relationship | Some | 4 | |
| Congenital suprabulbar paresis (disorder) | Interprets | Movement observable | true | Inferred relationship | Some | 3 | |
| Congenital suprabulbar paresis (disorder) | Has interpretation | Absent | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR