1335863008: Idiopathic scleritis (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of head region\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Head finding (finding)\Finding of head region\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Head finding (finding)\Finding of head region\Globe finding\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Head finding (finding)\Finding of head region\Globe finding\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Head finding (finding)\Finding of head region\Globe finding\Sclera and episclera finding\Disorder of sclera\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Head finding (finding)\Disorder of head (disorder)\Inflammatory disorder of head\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.

\Eye / vision finding\Globe finding\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Eye / vision finding\Globe finding\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Eye / vision finding\Globe finding\Sclera and episclera finding\Disorder of sclera\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Eye / vision finding\Visual system disorder (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Eye / vision finding\Visual system disorder (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.

\Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Disease\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Disease\Disorder of body system\Visual system disorder (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Disease\Disorder of body system\Visual system disorder (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammatory disorder of head\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body organs\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Disease\Disorder of head (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Disease\Disorder of head (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Disease\Disorder of head (disorder)\Inflammatory disorder of head\Inflammatory disorder of the eye\Scleritis\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.
\Disease\Idiopathic disease\A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jun 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

5361722010 A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5361723017 A rare form of scleritis characterized by tender or painful, violet-blueish eye, with edema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localization (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotizing). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5361720019 Idiopathic scleritis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5361721015 Idiopathic scleritis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.	Is a	Idiopathic disease	true	Inferred relationship	Some
A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.	Is a	Scleritis	true	Inferred relationship	Some
A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.	Finding site	Scleral structure	true	Inferred relationship	Some	1
A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.	Associated morphology	Inflammatory morphology (morphologic abnormality)	true	Inferred relationship	Some	1

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Refinability

Group

Reference Sets

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

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Id	Description	Lang	Type	Status	Case?	Module
5361722010	A rare form of scleritis characterised by tender or painful, violet-blueish eye, with oedema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localisation (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotising). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5361723017	A rare form of scleritis characterized by tender or painful, violet-blueish eye, with edema and injection of deep scleral vessels, in the absence of infection or systemic autoimmune diseases. The disease may be unilateral or bilateral. Other ocular signs depend on the localization (anterior or posterior) and on the type of scleritis (diffuse, nodular or necrotizing). Extension to other layers of the eye and to peri-ocular tissues as well as visual impairment are potential complications. Idiopathic scleritis is more frequent in children than in adults.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5361720019	Idiopathic scleritis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5361721015	Idiopathic scleritis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core