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715562001: Retinitis punctata albescens (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3303031016 Retinitis punctata albescens en Synonym Active Case insensitive SNOMED CT core


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 Some
Retinitis punctata albescens Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Retinitis punctata albescens Associated morphology Dystrophy true Inferred relationship Some 1
Retinitis punctata albescens 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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