51886007: Tritan defect (disorder)

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

Status: current, Primitive. 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	Case insensitive	SNOMED CT core
86387018	Tritan defect	en	Synonym	Active	Case insensitive	SNOMED CT core
86388011	Tritanomaly	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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