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711162004: Autosomal dominant vitreoretinochoroidopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2015. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3047554017 Autosomal dominant vitreoretinochoroidopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3047555016 Autosomal dominant vitreoretinochoroidopathy en Synonym Active Entire term case insensitive SNOMED CT core module
3078068010 Vitreoretinochoroidopathy with microcornea, glaucoma and cataract en Synonym Active Entire term case insensitive SNOMED CT core module
3078092019 Autosomal dominant vitreoretinochoroidopathy with nanophthalmos 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
Autosomal dominant vitreoretinochoroidopathy Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant vitreoretinochoroidopathy Is a Hereditary retinal dystrophy true Inferred relationship Existential restriction modifier
Autosomal dominant vitreoretinochoroidopathy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Autosomal dominant vitreoretinochoroidopathy Finding site Retinal structure 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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