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79556007: Vitreoretinal dystrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
131985018 Vitreoretinal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
820619014 Vitreoretinal dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5840661000172112 dystrophie vitréo-rétienne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4441081000172118 dystrofie van retina en corpus vitreum nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4441091000172115 vitreoretinale dystrofie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Vitreoretinal dystrophy Is a Hereditary retinal dystrophy true Inferred relationship Some
Vitreoretinal dystrophy Finding site Retinal structure false Inferred relationship Some
Vitreoretinal dystrophy Associated morphology Dystrophy true Inferred relationship Some 1
Vitreoretinal dystrophy Finding site Retinal structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Goldmann-Favre syndrome Is a True Vitreoretinal dystrophy Inferred relationship Some

This concept is not in any reference sets

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