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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


0 descendants.

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

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