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698847000: Hereditary retinal dystrophy primarily involving retinal pigment epithelium (disorder)


Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2981441013 Hereditary retinal dystrophy primarily involving retinal pigment epithelium en Synonym Active Case insensitive SNOMED CT core
2981448019 Hereditary retinal dystrophy primarily involving retinal pigment epithelium (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2981489016 Inherited retinal dystrophy primarily involving retinal pigment epithelium en Synonym Active Case insensitive SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary retinal dystrophy primarily involving retinal pigment epithelium Is a Hereditary retinal dystrophy true Inferred relationship Some
Hereditary retinal dystrophy primarily involving retinal pigment epithelium Finding site Retinal structure false Inferred relationship Some
Hereditary retinal dystrophy primarily involving retinal pigment epithelium Associated morphology Dystrophy true Inferred relationship Some 1
Hereditary retinal dystrophy primarily involving retinal pigment epithelium Finding site Retinal structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Biallelic RPE65 mutation associated retinal dystrophy Is a True Hereditary retinal dystrophy primarily involving retinal pigment epithelium Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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