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79556007: Vitreoretinal dystrophy (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
131985018 Vitreoretinal dystrophy en Synonym Active Case insensitive SNOMED CT core
820619014 Vitreoretinal dystrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core


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 Associated morphology Dystrophy true Inferred relationship Some 1
Vitreoretinal dystrophy Finding site Retinal structure true Inferred relationship Some 1
Vitreoretinal dystrophy Finding site Retinal structure false Inferred relationship Some

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

Reference Sets

Emergency department reference set

Australian emergency department reference set

NSW Emergency Department reference set

Clinical finding foundation reference set

Emergency department diagnosis reference set

Problem/Diagnosis reference set

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