Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
347716014 | Wagner syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
620080017 | Wagner syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Wagner syndrome | Is a | Hereditary vitreoretinopathy | true | Inferred relationship | Existential restriction modifier | ||
Wagner syndrome | Is a | Retinal disorder | false | Inferred relationship | Existential restriction modifier | ||
Wagner syndrome | Finding site | Vitreous body structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Wagner syndrome | Finding site | Retinal structure | true | Inferred relationship | Existential restriction modifier | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets