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51886007: Tritan defect (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
789834015 Tritan defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
86387018 Tritan defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
86388011 Tritanomaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Tritan defect (disorder) est un(e) (attribut) Congenital color blindness true Inferred relationship Some
Tritan defect (disorder) survenue (attribut) congénital false Inferred relationship Some
Tritan defect (disorder) interprète (attribut) entité observable de la vision false Inferred relationship Some 1
Tritan defect (disorder) a pour interprétation (attribut) anormal false Inferred relationship Some 1
Tritan defect (disorder) interprète (attribut) Visual function (observable entity) false Inferred relationship Some 1
Tritan defect (disorder) a pour interprétation (attribut) anormal false Inferred relationship Some 1
Tritan defect (disorder) interprète (attribut) Visual function (observable entity) false Inferred relationship Some 1
Tritan defect (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Tritan defect (disorder) localisation d'une constatation (attribut) structure de la rétine true Inferred relationship Some 1
Tritan defect (disorder) localisation d'une constatation (attribut) structure de la rétine false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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