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773727009: 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
5405398018 A rare, hereditary, non-syndromic form of vitreoretinopathy characterized by retinal tears due to abnormal vitreous, and commonly present refractive errors. No other signs or symptoms of Stickler syndrome is present. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5405399014 A rare, hereditary, non-syndromic form of vitreoretinopathy characterised by retinal tears due to abnormal vitreous, and commonly present refractive errors. No other signs or symptoms of Stickler syndrome is present. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
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
995851000172116 décollement de la rétine rhegmatogène autosomique dominant fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
545251000274113 Autosomal-dominante rhegmatogene Netzhautablösung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
603781000274113 Autosomal-dominante rhegmatogene Retinaablösung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare, hereditary, non-syndromic form of vitreoretinopathy characterized by retinal tears due to abnormal vitreous, and commonly present refractive errors. No other signs or symptoms of Stickler syndrome is present. Is a Hereditary disorder of the visual system true Inferred relationship Some
A rare, hereditary, non-syndromic form of vitreoretinopathy characterized by retinal tears due to abnormal vitreous, and commonly present refractive errors. No other signs or symptoms of Stickler syndrome is present. Is a Autosomal dominant hereditary disorder (disorder) true Inferred relationship Some
A rare, hereditary, non-syndromic form of vitreoretinopathy characterized by retinal tears due to abnormal vitreous, and commonly present refractive errors. No other signs or symptoms of Stickler syndrome is present. Is a Rhegmatogenous retinal detachment true Inferred relationship Some
A rare, hereditary, non-syndromic form of vitreoretinopathy characterized by retinal tears due to abnormal vitreous, and commonly present refractive errors. No other signs or symptoms of Stickler syndrome is present. Finding site Retinal structure true Inferred relationship Some 1
A rare, hereditary, non-syndromic form of vitreoretinopathy characterized by retinal tears due to abnormal vitreous, and commonly present refractive errors. No other signs or symptoms of Stickler syndrome is present. Associated morphology Separation true Inferred relationship Some 1
A rare, hereditary, non-syndromic form of vitreoretinopathy characterized by retinal tears due to abnormal vitreous, and commonly present refractive errors. No other signs or symptoms of Stickler syndrome is present. Due to Break of retina (disorder) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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