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715562001: Retinitis punctata albescens (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303030015 Retinitis punctata albescens (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303031016 Retinitis punctata albescens en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3869271000052115 retinitis punctata albescens 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
Retinitis punctata albescens (disorder) Is a Hereditary retinal dystrophy true Inferred relationship Some
Retinitis punctata albescens (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Retinitis punctata albescens (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Retinitis punctata albescens (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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