FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

232064001: Wagner syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
347716014 Wagner syndrome en Synonym Active Case sensitive SNOMED CT core
620080017 Wagner syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Back to Start