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232064001: Wagner syndrome (disorder)


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

Descriptions:

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


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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