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 |
| 3305549013 | A form of cerebral palsy with characteristics of congenital pseudobulbar (suprabulbar) paresis manifesting as selective weakness of the lips, tongue and soft palate, dysphagia, dysphonia, drooling and jaw jerking. Mean age at diagnosis is 6 years. The main clinical features are spasticity and limited movements around the mouth and throat from an early age, and brisk jaw jerks. Most cases are sporadic but several families with more than one affected member have been reported. Inheritance in these families appeared to follow an autosomal dominant pattern with variable expression and penetrance. | 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 | anomalie du développement | 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 |
This concept is not in any reference sets
FHIR