51886007: Tritan defect (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of head region\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect (disorder)
\Head finding (finding)\Finding of head region\Globe finding (finding)\Retina finding (finding)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect (disorder)
\Head finding (finding)\Finding of head region\Globe finding (finding)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect (disorder)

\Eye / vision finding\Globe finding (finding)\Retina finding (finding)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect (disorder)
\Eye / vision finding\Globe finding (finding)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect (disorder)
\Eye / vision finding\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect (disorder)
\Eye / vision finding\Visual system disorder\Disorder of vision (disorder)\Color vision deficiency (disorder)\Congenital color blindness\Tritan defect (disorder)
\Eye / vision finding\Visual system disorder\Disorder of vision (disorder)\Visual disturbance (disorder)\Colour blindness\Congenital color blindness\Tritan defect (disorder)

\Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital color blindness\Tritan defect (disorder)
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\Tritan defect (disorder)
\Disease\Disorder of body system\Visual system disorder\Disorder of vision (disorder)\Color vision deficiency (disorder)\Congenital color blindness\Tritan defect (disorder)
\Disease\Disorder of body system\Visual system disorder\Disorder of vision (disorder)\Visual disturbance (disorder)\Colour blindness\Congenital color blindness\Tritan defect (disorder)
\Disease\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and retina (disorder)\Retinal disorder\Colour blindness\Congenital color blindness\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:

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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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
86387018	Tritan defect	en	Synonym (core metadata concept)	Active	Only initial character 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	Only initial character 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	Only initial character 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
531281000274116	Tritanomalie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4559271000241114	tritanomalie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4559271000241114	tritanomalie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
531281000274116	Tritanomalie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module