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232065000: Goldmann-Favre syndrome (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
347717017 Goldmann-Favre syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
620082013 Goldmann-Favre syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
5072496019 Enhanced S-cone syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
5072497011 Retinoschisis with early nyctalopia en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Goldmann-Favre syndrome Is a Retinal disorder false Inferred relationship Existential restriction modifier
Goldmann-Favre syndrome Is a Hereditary vitreoretinopathy false Inferred relationship Existential restriction modifier
Goldmann-Favre syndrome Finding site Vitreous body structure true Inferred relationship Existential restriction modifier 1
Goldmann-Favre syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier 2
Goldmann-Favre syndrome Is a Chronic disease of ocular adnexa true Inferred relationship Existential restriction modifier
Goldmann-Favre syndrome Is a Connective tissue hereditary disorder true Inferred relationship Existential restriction modifier
Goldmann-Favre syndrome Is a Vitreous degeneration true Inferred relationship Existential restriction modifier
Goldmann-Favre syndrome Is a Vitreoretinal dystrophy true Inferred relationship Existential restriction modifier
Goldmann-Favre syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Goldmann-Favre syndrome Clinical course Progressive true Inferred relationship Existential restriction modifier 3
Goldmann-Favre syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 2
Goldmann-Favre syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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