Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3641817018 | Best vitelliform macular dystrophy (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3641818011 | Best vitelliform macular dystrophy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3641838012 | Best disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3641839016 | Polymorphic vitelline macular degeneration | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3641840019 | Early-onset vitelliform macular dystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5168741017 | Juvenile-onset vitelliform macular dystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5168742012 | BMD - Best macular dystrophy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5168743019 | Vitelliform macular dystrophy type 2 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5168744013 | BVMD - Best vitelliform macular dystrophy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5404054019 | Best vitelliform macular dystrophy (BVMD) is a genetic macular dystrophy characterized by loss of central visual acuity, metamorphopsia and a decrease in the Arden ratio secondary to an egg yolk-like lesion located in the foveal or parafoveal region. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5404055018 | Best vitelliform macular dystrophy (BVMD) is a genetic macular dystrophy characterised by loss of central visual acuity, metamorphopsia and a decrease in the Arden ratio secondary to an egg yolk-like lesion located in the foveal or parafoveal region. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Best vitelliform macular dystrophy (disorder) | Is a | Autosomal hereditary disorder | false | Inferred relationship | Some | ||
Best vitelliform macular dystrophy (disorder) | Is a | Vitelliform dystrophy | false | Inferred relationship | Some | ||
Best vitelliform macular dystrophy (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 1 | |
Best vitelliform macular dystrophy (disorder) | Finding site | Macula lutea structure | true | Inferred relationship | Some | 1 | |
Best vitelliform macular dystrophy (disorder) | Due to | Macular vitelliform deposits | false | Inferred relationship | Some | 2 | |
Best vitelliform macular dystrophy (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Best vitelliform macular dystrophy (disorder) | Is a | Macular vitelliform deposits | true | Inferred relationship | Some | ||
Best vitelliform macular dystrophy (disorder) | Is a | Chronic disease | true | Inferred relationship | Some | ||
Best vitelliform macular dystrophy (disorder) | Is a | Retinal dystrophy | true | Inferred relationship | Some | ||
Best vitelliform macular dystrophy (disorder) | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
Best vitelliform macular dystrophy (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 3 | |
Best vitelliform macular dystrophy (disorder) | Occurrence | Childhood | true | Inferred relationship | Some | 1 | |
Best vitelliform macular dystrophy (disorder) | Associated morphology | Deposition | true | Inferred relationship | Some | 1 | |
Best vitelliform macular dystrophy (disorder) | Occurrence | Childhood | true | Inferred relationship | Some | 2 | |
Best vitelliform macular dystrophy (disorder) | Finding site | Macula lutea structure | true | Inferred relationship | Some | 2 | |
Best vitelliform macular dystrophy (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 2 | |
Best vitelliform macular dystrophy (disorder) | Is a | Degenerative disorder of macula (disorder) | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)