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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
347840013 Congenital color blindness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
347841012 Congenital colour blindness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
620175012 Congenital color blindness (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


7 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 (disorder) 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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