Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3702807011 | Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3702808018 | Autosomal dominant neovascular inflammatory vitreoretinopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5404937012 | A rare, genetic, vitreoretinal degeneration characterized by a slowly progressive vitreoretinopathy with onset during the second or third decade of life. The disease initially presents as autoimmune uveitis with reduction in the b-wave on electroretinography, and progresses with development of photoreceptor degeneration, vitreous hemorrhage, cystoid macular edema, retinal neovascularization, intraocular fibrosis, secondary glaucoma, and retinal detachment leading to phthisis and complete blindness. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5404938019 | A rare, genetic, vitreoretinal degeneration characterised by a slowly progressive vitreoretinopathy with onset during the second or third decade of life. The disease initially presents as autoimmune uveitis with reduction in the b-wave on electroretinography, and progresses with development of photoreceptor degeneration, vitreous haemorrhage, cystoid macular oedema, retinal neovascularisation, intraocular fibrosis, secondary glaucoma, and retinal detachment leading to phthisis and complete blindness. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | Is a | Chronic disease | false | Inferred relationship | Some | ||
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | Is a | Vitreoretinal degeneration | true | Inferred relationship | Some | ||
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 3 | |
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 2 | |
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | Finding site | Peripheral retina | true | Inferred relationship | Some | 2 | |
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | Finding site | Vitreous body structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | Is a | Chronic disease of ocular adnexa | true | Inferred relationship | Some | ||
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 1 | |
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) | Is a | Connective tissue hereditary disorder (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)