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711162004: Autosomal dominant vitreoretinochoroidopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
3047555016 Autosomal dominant vitreoretinochoroidopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3078068010 Vitreoretinochoroidopathy with microcornea, glaucoma and cataract en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3078092019 Autosomal dominant vitreoretinochoroidopathy with nanophthalmos en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3808451000052116 autosomalt dominant vitreoretinokoroidopati sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant vitreoretinochoroidopathy (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant vitreoretinochoroidopathy (disorder) Is a Hereditary retinal dystrophy true Inferred relationship Some
Autosomal dominant vitreoretinochoroidopathy (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal dominant vitreoretinochoroidopathy (disorder) Finding site Retinal structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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