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698847000: hereditaire retinadystrofie van voornamelijk retinaal pigmentepitheel (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2981448019 Hereditary retinal dystrophy primarily involving retinal pigment epithelium (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2981489016 Inherited retinal dystrophy primarily involving retinal pigment epithelium en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6505441000146115 hereditaire retinadystrofie van voornamelijk retinaal pigmentepitheel nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6505451000146117 hereditaire retinadystrofie van voornamelijk retinaal pigmentepitheel (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


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, retinoid isomerohydrolase mutation associated retinal dystrophy (disorder) Is a True Hereditary retinal dystrophy primarily involving retinal pigment epithelium Inferred relationship Some

This concept is not in any reference sets

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