Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3726004011 | Autosomal dominant rhegmatogenous retinal detachment (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3726005012 | Autosomal dominant rhegmatogenous retinal detachment | en | Synonym | Active | Case insensitive | SNOMED CT core |
3726006013 | A rare hereditary non-syndromic form of vitreoretinopathy with characteristics of retinal tears due to abnormal vitreous and commonly present refractive errors. No other signs or symptoms of Stickler syndrome are present. Can be caused by mutation in the COL2A1 gene. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant rhegmatogenous retinal detachment | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Some | ||
Autosomal dominant rhegmatogenous retinal detachment | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant rhegmatogenous retinal detachment | Is a | Rhegmatogenous retinal detachment | true | Inferred relationship | Some | ||
Autosomal dominant rhegmatogenous retinal detachment | Finding site | Retinal structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant rhegmatogenous retinal detachment | Associated morphology | Separation | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set