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770791000: Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3702808018 Autosomal dominant neovascular inflammatory vitreoretinopathy en Synonym Active Case insensitive 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 Case sensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant neovascular inflammatory vitreoretinopathy Is a Chronic disease of ocular adnexa true Inferred relationship Some
Autosomal dominant neovascular inflammatory vitreoretinopathy Associated morphology Atrophy true Inferred relationship Some 1
Autosomal dominant neovascular inflammatory vitreoretinopathy Is a Inherited disorder of connective tissue true Inferred relationship Some
Autosomal dominant neovascular inflammatory vitreoretinopathy Is a Chronic disease false Inferred relationship Some
Autosomal dominant neovascular inflammatory vitreoretinopathy Is a Vitreoretinal degeneration true Inferred relationship Some
Autosomal dominant neovascular inflammatory vitreoretinopathy Is a Hereditary disorder of the visual system true Inferred relationship Some
Autosomal dominant neovascular inflammatory vitreoretinopathy Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant neovascular inflammatory vitreoretinopathy Clinical course Progressive true Inferred relationship Some 3
Autosomal dominant neovascular inflammatory vitreoretinopathy Associated morphology Atrophy true Inferred relationship Some 2
Autosomal dominant neovascular inflammatory vitreoretinopathy Finding site Peripheral retina true Inferred relationship Some 2
Autosomal dominant neovascular inflammatory vitreoretinopathy Associated morphology Degeneration false Inferred relationship Some 1
Autosomal dominant neovascular inflammatory vitreoretinopathy Finding site Vitreous body 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

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