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232148006: Congenital color blindness (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
347840013 Congenital color blindness en Synonym Active Case insensitive SNOMED CT core
347841012 Congenital colour blindness en Synonym Active Case insensitive SNOMED CT core
620175012 Congenital color blindness (disorder) en Fully specified name Active Case insensitive SNOMED CT core


7 descendants. Search Descendants:

Expanded Value Set


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

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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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