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1231183003: Familial isolated retinal arterial tortuosity (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5071804017 Familial isolated retinal arterial tortuosity (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5071805016 Familial isolated retinal arterial tortuosity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5071806015 Retinal hemorrhage with vascular tortuosity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5071807012 Tortuosity of retinal arteries en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5071808019 Retinal haemorrhage with vascular tortuosity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5071809010 Retinal arteriolar tortuosity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5071811018 A rare genetic cerebral small vessel disease with isolated marked tortuosity of second order and third order retinal arteries with normal first order arteries and venous system, typically located in the macular and peripapillary area and developing during childhood or early adulthood. The disease may be asymptomatic, although most patients present variable degrees of transient vision loss due to retinal hemorrhage following physical exertion or minor trauma. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5071812013 A rare genetic cerebral small vessel disease with isolated marked tortuosity of second order and third order retinal arteries with normal first order arteries and venous system, typically located in the macular and peripapillary area and developing during childhood or early adulthood. The disease may be asymptomatic, although most patients present variable degrees of transient vision loss due to retinal haemorrhage following physical exertion or minor trauma. 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
Familial isolated retinal arterial tortuosity (disorder) est un(e) (attribut) Retinal arterial tortuosity true Inferred relationship Some
Familial isolated retinal arterial tortuosity (disorder) est un(e) (attribut) Tortuosity of systemic artery (disorder) true Inferred relationship Some
Familial isolated retinal arterial tortuosity (disorder) est un(e) (attribut) Disease of non-coronary systemic artery true Inferred relationship Some
Familial isolated retinal arterial tortuosity (disorder) est un(e) (attribut) trouble vasculaire rétinien true Inferred relationship Some
Familial isolated retinal arterial tortuosity (disorder) est un(e) (attribut) Deformity of eyeball true Inferred relationship Some
Familial isolated retinal arterial tortuosity (disorder) est un(e) (attribut) Genetic disease true Inferred relationship Some
Familial isolated retinal arterial tortuosity (disorder) localisation d'une constatation (attribut) artère rétinienne (structure corporelle) true Inferred relationship Some 1
Familial isolated retinal arterial tortuosity (disorder) morphologie associée (attribut) Tortuosity true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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