Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3047555016 | Autosomal dominant vitreoretinochoroidopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3078068010 | Vitreoretinochoroidopathy with microcornea, glaucoma and cataract | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3078092019 | Autosomal dominant vitreoretinochoroidopathy with nanophthalmos | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3808451000052116 | autosomalt dominant vitreoretinokoroidopati | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant vitreoretinochoroidopathy (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant vitreoretinochoroidopathy (disorder) | Is a | Hereditary retinal dystrophy | true | Inferred relationship | Some | ||
Autosomal dominant vitreoretinochoroidopathy (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal dominant vitreoretinochoroidopathy (disorder) | Finding site | Retinal structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets