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51445007: Protan defect (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
789345011 Protan defect (disorder) en Fully specified name Active Case sensitive SNOMED CT core
85680019 Protan defect en Synonym Active Case sensitive SNOMED CT core
85681015 Protanomaly en Synonym Active Case insensitive SNOMED CT core
85682010 Protanopia en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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