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770791000: Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder)


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
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
3702809014 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. Caused by heterozygous mutation in the CAPN5 gene on chromosome 11q14. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3702810016 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. Caused by heterozygous mutation in the CAPN5 gene on chromosome 11q14. en Definition Active Entire term case sensitive (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
544371000274113 ADNIV - Autosomal-dominante neovaskuläre inflammatorische Vitreoretinopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
574761000274117 Autosomal-dominante neovaskuläre inflammatorische Vitreoretinopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
939471000172118 vitréorétinopathie inflammatoire néovasculaire autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1001871000172117 ADNIV - autosomal dominant neovascular inflammatory vitreoretinopathy fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
939471000172118 vitréorétinopathie inflammatoire néovasculaire autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1001871000172117 ADNIV - autosomal dominant neovascular inflammatory vitreoretinopathy fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
544371000274113 ADNIV - Autosomal-dominante neovaskuläre inflammatorische Vitreoretinopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
574761000274117 Autosomal-dominante neovaskuläre inflammatorische Vitreoretinopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3431761001000114 Vitreoretinopathie, inflammatorische neovaskuläre, autosomal-dominante de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Is a Chronic disease false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Is a Vitreoretinal degeneration true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Associated morphology Atrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Finding site Peripheral retina true Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Finding site Vitreous body structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Is a Chronic disease of ocular adnexa true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Associated morphology Atrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Is a Connective tissue hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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