Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 347716014 | Wagner syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 620080017 | Wagner syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Wagner syndrome | Is a | Hereditary vitreoretinopathy | true | Inferred relationship | Some | ||
| Wagner syndrome | Is a | Retinal disorder | false | Inferred relationship | Some | ||
| Wagner syndrome | Finding site | Vitreous body structure | true | Inferred relationship | Some | 1 | |
| Wagner syndrome | Finding site | Retinal structure | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set