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51445007: protanomalie (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
85680019 Protan defect en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
85681015 Protanomaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
85682010 Protanopia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
789345011 Protan defect (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1891801000146119 protanomalie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
1891811000146117 protanomalie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13081731000146111 Vorm van kleurenblindheid waarbij iemand minder gevoelig is voor de kleur rood. nl Definition 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
Protan defect Is a Congenital color blindness true Inferred relationship Some
Protan defect Finding site Retinal structure false 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 (observable entity) 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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Dutch optometric diagnoses simple reference set (foundation metadata concept)

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