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


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module

Descriptions:

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


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 Existential restriction modifier
Hereditary retinal dystrophy primarily involving retinal pigment epithelium Finding site Retinal structure false Inferred relationship Existential restriction modifier
Hereditary retinal dystrophy primarily involving retinal pigment epithelium Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Hereditary retinal dystrophy primarily involving retinal pigment epithelium Finding site Retinal structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Biallelic RPE65, retinoid isomerohydrolase mutation associated retinal dystrophy Is a True Hereditary retinal dystrophy primarily involving retinal pigment epithelium Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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