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773727009: Autosomal dominant rhegmatogenous retinal detachment (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3726005012 Autosomal dominant rhegmatogenous retinal detachment en Synonym Active Case insensitive 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 Case sensitive SNOMED CT core


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 true Inferred relationship Some
Autosomal dominant rhegmatogenous retinal detachment Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant rhegmatogenous retinal detachment Is a Rhegmatogenous retinal detachment true Inferred relationship Some
Autosomal dominant rhegmatogenous retinal detachment Finding site Retinal structure true Inferred relationship Some 1
Autosomal dominant rhegmatogenous retinal detachment Associated morphology Separation true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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