Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
347713018 | Hereditary vitreoretinopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
620078011 | Hereditary vitreoretinopathy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary vitreoretinopathy | Is a | Inherited disorder of connective tissue | true | Inferred relationship | Some | ||
Hereditary vitreoretinopathy | Is a | Retinopathy | false | Inferred relationship | Some | ||
Hereditary vitreoretinopathy | Finding site | Retinal structure | true | Inferred relationship | Some | 2 | |
Hereditary vitreoretinopathy | Is a | Disorder of vitreous body | true | Inferred relationship | Some | ||
Hereditary vitreoretinopathy | Finding site | Vitreous body structure | true | Inferred relationship | Some | 1 | |
Hereditary vitreoretinopathy | Is a | Retinal disorder | true | Inferred relationship | Some | ||
Hereditary vitreoretinopathy | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Stickler syndrome | Is a | True | Hereditary vitreoretinopathy | Inferred relationship | Some | |
Familial exudative vitreoretinopathy | Is a | True | Hereditary vitreoretinopathy | Inferred relationship | Some | |
Wagner syndrome | Is a | True | Hereditary vitreoretinopathy | Inferred relationship | Some | |
Goldmann-Favre syndrome | Is a | False | Hereditary vitreoretinopathy | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set