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51886007: Tritan defect (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
86387018 Tritan defect en Synonym Active Entire term case insensitive SNOMED CT core module
86388011 Tritanomaly en Synonym Active Entire term case insensitive SNOMED CT core module
789834015 Tritan defect (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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