FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

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


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
2981441013 Hereditary retinal dystrophy primarily involving retinal pigment epithelium en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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 Only initial character 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
515521000274111 Erbbedingte Netzhautdystrophie, retinales Pigmentepithel primär betroffen de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
599751000274114 Hereditäre Retinadystrophie, retinales Pigmentepithel primär betroffen de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6315181000241119 dystrophie rétinienne héréditaire impliquant principalement l'épithélium pigmentaire rétinien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6315191000241117 dystrophie héréditaire de la rétine impliquant principalement l'épithélium pigmentaire rétinien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6315181000241119 dystrophie rétinienne héréditaire impliquant principalement l'épithélium pigmentaire rétinien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6315191000241117 dystrophie héréditaire de la rétine impliquant principalement l'épithélium pigmentaire rétinien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
515521000274111 Erbbedingte Netzhautdystrophie, retinales Pigmentepithel primär betroffen de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
599751000274114 Hereditäre Retinadystrophie, retinales Pigmentepithel primär betroffen de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary retinal dystrophy primarily involving retinal pigment epithelium Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary retinal dystrophy primarily involving retinal pigment epithelium Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary retinal dystrophy primarily involving retinal pigment epithelium Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start