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232148006: Congenital color blindness (disorder)


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 Reference Sets
347840013 Congenital color blindness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core US English: Preferred (foundation metadata concept)
347841012 Congenital colour blindness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
620175012 Congenital color blindness (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)

6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital color blindness Is a Color vision deficiency (disorder) true Inferred relationship Some
Congenital color blindness Is a Colour blindness true Inferred relationship Some
Congenital color blindness Finding site Retinal structure false Inferred relationship Some
Congenital color blindness Is a Congenital anomaly of eye false Inferred relationship Some
Congenital color blindness Occurrence Congenital false Inferred relationship Some
Congenital color blindness Is a Congenital disease true Inferred relationship Some
Congenital color blindness Has interpretation Abnormal false Inferred relationship Some 1
Congenital color blindness Interprets Vision observable (observable entity) false Inferred relationship Some 1
Congenital color blindness Interprets Visual function false Inferred relationship Some 1
Congenital color blindness Has interpretation Abnormal false Inferred relationship Some 1
Congenital color blindness Interprets Visual function false Inferred relationship Some 1
Congenital color blindness Occurrence Congenital true Inferred relationship Some 1
Congenital color blindness Finding site Retinal structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Protan defect Is a True Congenital color blindness Inferred relationship Some
Tritan defect Is a True Congenital color blindness Inferred relationship Some
Achromatopsia Is a True Congenital color blindness Inferred relationship Some
Deutan defect Is a True Congenital color blindness Inferred relationship Some
Blue cone monochromatism (disorder) Is a True Congenital color blindness Inferred relationship Some

This concept is not in any reference sets

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