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

232062002: Hereditary vitreoretinopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
347713018 Hereditary vitreoretinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
620078011 Hereditary vitreoretinopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
347713018 Hereditary vitreoretinopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
347713018 Hereditary vitreoretinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
620078011 Hereditary vitreoretinopathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
620078011 Hereditary vitreoretinopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
543971000274114 Hereditäre Vitreoretinopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6252041000241119 vitréorétinopathie héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6252051000241116 VRH - vitréorétinopathie héréditaire fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6252041000241119 vitréorétinopathie héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6252051000241116 VRH - vitréorétinopathie héréditaire fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
543971000274114 Hereditäre Vitreoretinopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary vitreoretinopathy Is a Disorder of vitreous body true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary vitreoretinopathy Finding site Vitreous body structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary vitreoretinopathy Is a Retinopathy false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary vitreoretinopathy Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary vitreoretinopathy Is a Retinal disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary vitreoretinopathy Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary vitreoretinopathy Is a Connective tissue hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial exudative vitreoretinopathy Is a True Hereditary vitreoretinopathy Inferred relationship Existential restriction modifier (core metadata concept)
Wagner syndrome (disorder) Is a True Hereditary vitreoretinopathy Inferred relationship Existential restriction modifier (core metadata concept)
Goldmann-Favre syndrome Is a False Hereditary vitreoretinopathy Inferred relationship Existential restriction modifier (core metadata concept)
Stickler syndrome Is a True Hereditary vitreoretinopathy Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start