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783090002: Idiopathic retinal vasculitis, aneurysms, neuroretinitis syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3757545016 A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3757546015 A rare retinal vasculopathy disease characterized by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularization and macular exudation, leading to severe bilateral vision loss. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3757541013 Idiopathic retinal vasculitis, aneurysms, neuroretinitis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3757542018 Idiopathic retinal vasculitis, aneurysms, neuroretinitis syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3757543011 IRVAN (idiopathic retinal vasculitis, aneurysms, neuroretinitis) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3757544017 IRVAN syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Is a Idiopathic disease false Inferred relationship Some
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Associated morphology Inflammation false Inferred relationship Some 2
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Is a Retinal vasculitis true Inferred relationship Some
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Is a Arterial aneurysm true Inferred relationship Some
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Finding site Optic disc structure true Inferred relationship Some 2
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Is a Neuroretinitis (disorder) true Inferred relationship Some
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Associated morphology Aneurysm true Inferred relationship Some 3
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Finding site Structure of blood vessel of retina true Inferred relationship Some 1
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Finding site Arterial structure true Inferred relationship Some 3
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Associated morphology Inflammation false Inferred relationship Some 1
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Some 2
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Some 1
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Is a Idiopathic retinitis true Inferred relationship Some
A rare retinal vasculopathy disease characterised by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion retinal neovascularisation and macular exudation, leading to severe bilateral vision loss. Is a Idiopathic optic neuritis true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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