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79556007: Vitreoretinal dystrophy (disorder)


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

Descriptions:

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


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 Existential restriction modifier
Vitreoretinal dystrophy Finding site Retinal structure false Inferred relationship Existential restriction modifier
Vitreoretinal dystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Vitreoretinal dystrophy Finding site Retinal structure true Inferred relationship Existential restriction modifier 1

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

This concept is not in any reference sets

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