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1234824005: Acute macular neuroretinopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5400223017 A rare, acquired retinal disorder characterized by transient or permanent visual impairment accompanied by the presence of reddish-brown, wedge-shaped lesions in the macula, the apices of which tend to point towards the fovea. The lesions usually appear in a petaloid or tear-drop configuration. Patients tend to be young, Caucasian, and female. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400224011 A rare, acquired retinal disorder characterised by transient or permanent visual impairment accompanied by the presence of reddish-brown, wedge-shaped lesions in the macula, the apices of which tend to point towards the fovea. The lesions usually appear in a petaloid or tear-drop configuration. Patients tend to be young, Caucasian, and female. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5084145018 Acute macular neuroretinopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5084146017 Acute macular neuroretinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5084147014 AMNR - acute macular neuroretinopathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
529971000274114 AMNR - Akute makuläre Neuroretinopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
594661000274117 Akute makuläre Neuroretinopathie 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, acquired retinal disorder characterized by transient or permanent visual impairment accompanied by the presence of reddish-brown, wedge-shaped lesions in the macula, the apices of which tend to point towards the fovea. The lesions usually appear in a petaloid or tear-drop configuration. Patients tend to be young, Caucasian, and female. Is a Acute disease of eye true Inferred relationship Some
A rare, acquired retinal disorder characterized by transient or permanent visual impairment accompanied by the presence of reddish-brown, wedge-shaped lesions in the macula, the apices of which tend to point towards the fovea. The lesions usually appear in a petaloid or tear-drop configuration. Patients tend to be young, Caucasian, and female. Is a Disorder of macula of retina (disorder) true Inferred relationship Some
A rare, acquired retinal disorder characterized by transient or permanent visual impairment accompanied by the presence of reddish-brown, wedge-shaped lesions in the macula, the apices of which tend to point towards the fovea. The lesions usually appear in a petaloid or tear-drop configuration. Patients tend to be young, Caucasian, and female. Clinical course Sudden onset AND/OR short duration (qualifier value) true Inferred relationship Some 2
A rare, acquired retinal disorder characterized by transient or permanent visual impairment accompanied by the presence of reddish-brown, wedge-shaped lesions in the macula, the apices of which tend to point towards the fovea. The lesions usually appear in a petaloid or tear-drop configuration. Patients tend to be young, Caucasian, and female. Occurrence Any period of life commencing after birth, but before death. true Inferred relationship Some 1
A rare, acquired retinal disorder characterized by transient or permanent visual impairment accompanied by the presence of reddish-brown, wedge-shaped lesions in the macula, the apices of which tend to point towards the fovea. The lesions usually appear in a petaloid or tear-drop configuration. Patients tend to be young, Caucasian, and female. Finding site Macula lutea structure true Inferred relationship Some 1
A rare, acquired retinal disorder characterized by transient or permanent visual impairment accompanied by the presence of reddish-brown, wedge-shaped lesions in the macula, the apices of which tend to point towards the fovea. The lesions usually appear in a petaloid or tear-drop configuration. Patients tend to be young, Caucasian, and female. Is a Anomaly of eye (disorder) false Inferred relationship Some
A rare, acquired retinal disorder characterized by transient or permanent visual impairment accompanied by the presence of reddish-brown, wedge-shaped lesions in the macula, the apices of which tend to point towards the fovea. The lesions usually appear in a petaloid or tear-drop configuration. Patients tend to be young, Caucasian, and female. Is a Lesion of eye (disorder) false Inferred relationship Some
A rare, acquired retinal disorder characterized by transient or permanent visual impairment accompanied by the presence of reddish-brown, wedge-shaped lesions in the macula, the apices of which tend to point towards the fovea. The lesions usually appear in a petaloid or tear-drop configuration. Patients tend to be young, Caucasian, and female. Associated morphology Lesion (morphologic abnormality) true Inferred relationship Some 1
A rare, acquired retinal disorder characterized by transient or permanent visual impairment accompanied by the presence of reddish-brown, wedge-shaped lesions in the macula, the apices of which tend to point towards the fovea. The lesions usually appear in a petaloid or tear-drop configuration. Patients tend to be young, Caucasian, and female. Is a Lesion of retina true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

Description inactivation indicator reference set

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