715339004: Autosomal dominant keratitis (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 (disorder)\Keratitis\Autosomal dominant keratitis (disorder)
\Head finding (finding)\Finding of head region\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of anterior segment of eye\Disorder of cornea\Keratitis\Autosomal dominant keratitis (disorder)
\Head finding (finding)\Finding of head region\Globe finding\Anterior segment finding (finding)\Corneal finding\Disorder of cornea\Keratitis\Autosomal dominant keratitis (disorder)
\Head finding (finding)\Finding of head region\Globe finding\Anterior segment finding (finding)\Disorder of anterior segment of eye\Disorder of cornea\Keratitis\Autosomal dominant keratitis (disorder)
\Head finding (finding)\Finding of head region\Globe finding\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye (disorder)\Keratitis\Autosomal dominant keratitis (disorder)
\Head finding (finding)\Finding of head region\Globe finding\Disorder of eye proper (disorder)\Disorder of anterior segment of eye\Disorder of cornea\Keratitis\Autosomal dominant keratitis (disorder)
\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 (disorder)\Keratitis\Autosomal dominant keratitis (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of anterior segment of eye\Disorder of cornea\Keratitis\Autosomal dominant keratitis (disorder)
\Head finding (finding)\Disorder of head (disorder)\Inflammatory disorder of head\Inflammatory disorder of the eye (disorder)\Keratitis\Autosomal dominant keratitis (disorder)

\Eye / vision finding\Globe finding\Anterior segment finding (finding)\Corneal finding\Disorder of cornea\Keratitis\Autosomal dominant keratitis (disorder)
\Eye / vision finding\Globe finding\Anterior segment finding (finding)\Disorder of anterior segment of eye\Disorder of cornea\Keratitis\Autosomal dominant keratitis (disorder)
\Eye / vision finding\Globe finding\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye (disorder)\Keratitis\Autosomal dominant keratitis (disorder)
\Eye / vision finding\Globe finding\Disorder of eye proper (disorder)\Disorder of anterior segment of eye\Disorder of cornea\Keratitis\Autosomal dominant keratitis (disorder)
\Eye / vision finding\Visual system disorder\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye (disorder)\Keratitis\Autosomal dominant keratitis (disorder)
\Eye / vision finding\Visual system disorder\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of anterior segment of eye\Disorder of cornea\Keratitis\Autosomal dominant keratitis (disorder)
\Eye / vision finding\Visual system disorder\Hereditary disorder of the visual system (disorder)\Autosomal dominant keratitis (disorder)

\Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye (disorder)\Keratitis\Autosomal dominant keratitis (disorder)
\Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Disorder of anterior segment of eye\Disorder of cornea\Keratitis\Autosomal dominant keratitis (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the visual system (disorder)\Autosomal dominant keratitis (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant keratitis (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Autosomal dominant keratitis (disorder)
\Disease\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of the eye (disorder)\Keratitis\Autosomal dominant keratitis (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the visual system (disorder)\Autosomal dominant keratitis (disorder)
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye (disorder)\Keratitis\Autosomal dominant keratitis (disorder)
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of anterior segment of eye\Disorder of cornea\Keratitis\Autosomal dominant keratitis (disorder)
\Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system (disorder)\Autosomal dominant keratitis (disorder)
\Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammatory disorder of head\Inflammatory disorder of the eye (disorder)\Keratitis\Autosomal dominant keratitis (disorder)
\Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of the eye (disorder)\Keratitis\Autosomal dominant keratitis (disorder)
\Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body organs\Inflammatory disorder of the eye (disorder)\Keratitis\Autosomal dominant keratitis (disorder)
\Disease\Disorder of head (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Inflammatory disorder of the eye (disorder)\Keratitis\Autosomal dominant keratitis (disorder)
\Disease\Disorder of head (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of anterior segment of eye\Disorder of cornea\Keratitis\Autosomal dominant keratitis (disorder)
\Disease\Disorder of head (disorder)\Inflammatory disorder of head\Inflammatory disorder of the eye (disorder)\Keratitis\Autosomal dominant keratitis (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3302274016 Autosomal dominant keratitis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3302275015 Autosomal dominant keratitis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3302276019 Hereditary keratitis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5400826016 A rare genetic inflammatory corneal disorder characterized by anterior stromal corneal opacification and vascularization of the peripheral cornea with potential central progression and subsequent reduction in visual acuity. Variable features include abnormalities of the iris, such as stromal defects and ectropion uveae, as well as foveal hypoplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5400827013 A rare genetic inflammatory corneal disorder characterised by anterior stromal corneal opacification and vascularisation of the peripheral cornea with potential central progression and subsequent reduction in visual acuity. Variable features include abnormalities of the iris, such as stromal defects and ectropion uveae, as well as foveal hypoplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Autosomal dominant keratitis (disorder)	Is a	Keratitis	true	Inferred relationship	Some
Autosomal dominant keratitis (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Autosomal dominant keratitis (disorder)	Is a	Congenital disease (disorder)	true	Inferred relationship	Some
Autosomal dominant keratitis (disorder)	Is a	Hereditary disorder of the visual system (disorder)	true	Inferred relationship	Some
Autosomal dominant keratitis (disorder)	Associated morphology	Inflammation	false	Inferred relationship	Some	1
Autosomal dominant keratitis (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Autosomal dominant keratitis (disorder)	Finding site	Corneal structure	true	Inferred relationship	Some	1
Autosomal dominant keratitis (disorder)	Associated morphology	Inflammatory morphology (morphologic abnormality)	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

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

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3302274016	Autosomal dominant keratitis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3302275015	Autosomal dominant keratitis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3302276019	Hereditary keratitis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5400826016	A rare genetic inflammatory corneal disorder characterized by anterior stromal corneal opacification and vascularization of the peripheral cornea with potential central progression and subsequent reduction in visual acuity. Variable features include abnormalities of the iris, such as stromal defects and ectropion uveae, as well as foveal hypoplasia.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5400827013	A rare genetic inflammatory corneal disorder characterised by anterior stromal corneal opacification and vascularisation of the peripheral cornea with potential central progression and subsequent reduction in visual acuity. Variable features include abnormalities of the iris, such as stromal defects and ectropion uveae, as well as foveal hypoplasia.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core