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715562001: Retinitis punctata albescens (disorder)


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

Descriptions:

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