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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
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
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
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
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
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
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
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
3441661001000119 Netzhautablösung, rhegmatogene, autosomal-dominante 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
Autosomal dominant rhegmatogenous retinal detachment Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant rhegmatogenous retinal detachment Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant rhegmatogenous retinal detachment Is a Rhegmatogenous retinal detachment true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant rhegmatogenous retinal detachment Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant rhegmatogenous retinal detachment Associated morphology Separation true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant rhegmatogenous retinal detachment Due to Break of retina (disorder) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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