FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

232064001: Wagner-syndroom (aandoening)


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
347716014 Wagner syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
620080017 Wagner syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
58581000146110 syndroom van Wagner nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
2224051000146113 Wagner-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10672871000146114 Wagner-syndroom (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Wagner syndrome (disorder) Is a Hereditary vitreoretinopathy true Inferred relationship Some
Wagner syndrome (disorder) Is a Retinal disorder false Inferred relationship Some
Wagner syndrome (disorder) Finding site Vitreous body structure true Inferred relationship Some 1
Wagner syndrome (disorder) Finding site Retinal structure true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

GB English

US English

Back to Start