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77479002: Deutan defect (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
128623010 Deutan defect en Synonym Active Case insensitive SNOMED CT core
128624016 Deuteranomaly en Synonym Active Case insensitive SNOMED CT core
128625015 Deuteranopia en Synonym Active Case insensitive SNOMED CT core
818313015 Deutan defect (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deutan defect Occurrence Congenital false Inferred relationship Some
Deutan defect Has interpretation Abnormal false Inferred relationship Some 1
Deutan defect Interprets Vision observable false Inferred relationship Some 1
Deutan defect Is a Congenital colour blindness true Inferred relationship Some
Deutan defect Interprets Visual function false Inferred relationship Some 1
Deutan defect Interprets Visual function false Inferred relationship Some 1
Deutan defect Has interpretation Abnormal false Inferred relationship Some 1
Deutan defect Occurrence Congenital true Inferred relationship Some 1
Deutan defect Finding site Retinal structure true Inferred relationship Some 1
Deutan defect Finding site Retinal structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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