773727009: autosomaal dominante regmatogene netvliesloslating (aandoening)

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

\Head finding (finding)\Finding of head region\Finding of eye region\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Lesion of eye (disorder)\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Head finding (finding)\Finding of head region\Finding of eye region\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Head finding (finding)\Finding of head region\Finding of eye region\Globe finding\Retina finding (finding)\Retinal disorder\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Head finding (finding)\Finding of head region\Finding of eye region\Globe finding\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Lesion of eye (disorder)\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Head finding (finding)\Finding of head region\Finding of eye region\Globe finding\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Lesion of eye (disorder)\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)

\Eye / vision finding\Finding of eye region\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Lesion of eye (disorder)\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Eye / vision finding\Finding of eye region\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Eye / vision finding\Finding of eye region\Globe finding\Retina finding (finding)\Retinal disorder\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Eye / vision finding\Finding of eye region\Globe finding\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Lesion of eye (disorder)\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Eye / vision finding\Finding of eye region\Globe finding\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Eye / vision finding\Visual system disorder\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Lesion of eye (disorder)\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Eye / vision finding\Visual system disorder\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Eye / vision finding\Visual system disorder\Hereditary disorder of the visual system (disorder)\Autosomal dominant rhegmatogenous retinal detachment (disorder)

\Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Lesion of eye (disorder)\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the visual system (disorder)\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the visual system (disorder)\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Lesion of eye (disorder)\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system (disorder)\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Disease\Disorder of head (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\Lesion of eye (disorder)\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (disorder)
\Disease\Disorder of head (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Lesion of retina\Retinal detachment\Rhegmatogenous retinal detachment\Autosomal dominant rhegmatogenous retinal detachment (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

3726004011 Autosomal dominant rhegmatogenous retinal detachment (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3726005012 Autosomal dominant rhegmatogenous retinal detachment en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

6545941000146116 autosomaal dominante regmatogene netvliesloslating (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6545951000146118 autosomaal dominante regmatogene netvliesloslating nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6545961000146115 autosomaal dominante regmatogene ablatio retinae nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

3726006013 A rare hereditary non-syndromic form of vitreoretinopathy with characteristics of retinal tears due to abnormal vitreous and commonly present refractive errors. No other signs or symptoms of Stickler syndrome are present. Can be caused by mutation in the COL2A1 gene. 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 rhegmatogenous retinal detachment (disorder)	Is a	Hereditary disorder of the visual system (disorder)	true	Inferred relationship	Some
Autosomal dominant rhegmatogenous retinal detachment (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Autosomal dominant rhegmatogenous retinal detachment (disorder)	Is a	Rhegmatogenous retinal detachment	true	Inferred relationship	Some
Autosomal dominant rhegmatogenous retinal detachment (disorder)	Finding site	Retinal structure	true	Inferred relationship	Some	1
Autosomal dominant rhegmatogenous retinal detachment (disorder)	Associated morphology	Separation (morphologic abnormality)	true	Inferred relationship	Some	1
Autosomal dominant rhegmatogenous retinal detachment (disorder)	Due to	Break of retina (disorder)	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3726004011	Autosomal dominant rhegmatogenous retinal detachment (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3726005012	Autosomal dominant rhegmatogenous retinal detachment	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6545941000146116	autosomaal dominante regmatogene netvliesloslating (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6545951000146118	autosomaal dominante regmatogene netvliesloslating	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6545961000146115	autosomaal dominante regmatogene ablatio retinae	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
3726006013	A rare hereditary non-syndromic form of vitreoretinopathy with characteristics of retinal tears due to abnormal vitreous and commonly present refractive errors. No other signs or symptoms of Stickler syndrome are present. Can be caused by mutation in the COL2A1 gene.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core