Status: current, Primitive. Date: 31-Jul 2015. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3047554017 | Autosomal dominant vitreoretinochoroidopathy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3047555016 | Autosomal dominant vitreoretinochoroidopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
3078068010 | Vitreoretinochoroidopathy with microcornea, glaucoma and cataract | en | Synonym | Active | Case insensitive | SNOMED CT core |
3078092019 | Autosomal dominant vitreoretinochoroidopathy with nanophthalmos | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant vitreoretinochoroidopathy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant vitreoretinochoroidopathy | Is a | Hereditary retinal dystrophy | true | Inferred relationship | Some | ||
Autosomal dominant vitreoretinochoroidopathy | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal dominant vitreoretinochoroidopathy | Finding site | Retinal structure | 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