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711162004: Autosomal dominant vitreoretinochoroidopathy (disorder)


Status: current, Primitive. Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3047554017 Autosomal dominant vitreoretinochoroidopathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3047555016 Autosomal dominant vitreoretinochoroidopathy en Synonym Active Case insensitive SNOMED CT core
3078068010 Vitreoretinochoroidopathy with microcornea, glaucoma and cataract en Synonym Active Case insensitive SNOMED CT core
3078092019 Autosomal dominant vitreoretinochoroidopathy with nanophthalmos en Synonym Active Case insensitive SNOMED CT core


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 Some
Autosomal dominant vitreoretinochoroidopathy Is a Hereditary retinal dystrophy true Inferred relationship Some
Autosomal dominant vitreoretinochoroidopathy Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal dominant vitreoretinochoroidopathy Finding site Retinal structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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