51886007: Tritan defect (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Finding of head and neck region\Head finding (finding)\...
• \Finding of head region\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect
• \Finding of head region\Globe finding\Retina finding (finding)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect
• \Finding of head region\Globe finding\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect
• \Disorder of head (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect
• \Eye / vision finding\Globe finding\Retina finding (finding)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect
• \Eye / vision finding\Globe finding\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect
• \Eye / vision finding\Visual system disorder\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect
• \Eye / vision finding\Visual system disorder\Disorder of vision\Color vision deficiency (disorder)\Congenital color blindness\Tritan defect
• \Eye / vision finding\Visual system disorder\Disorder of vision\Visual disturbance\Colour blindness\Congenital color blindness\Tritan defect
• \Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect
• \Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital color blindness\Tritan defect
• \Disease\Disorder of body system\Visual system disorder\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect
• \Disease\Disorder of body system\Visual system disorder\Disorder of vision\Color vision deficiency (disorder)\Congenital color blindness\Tritan defect
• \Disease\Disorder of body system\Visual system disorder\Disorder of vision\Visual disturbance\Colour blindness\Congenital color blindness\Tritan defect
• \Disease\Disorder of head (disorder)\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect

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
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
789834015	Tritan defect (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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