232148006: Congenital color blindness (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
\Head finding (finding)\Finding of head region\Globe finding (finding)\Retina finding (finding)\Retinal disorder\Colour blindness\Congenital color blindness
\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
\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

\Eye / vision finding\Globe finding (finding)\Retina finding (finding)\Retinal disorder\Colour blindness\Congenital color blindness
\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
\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
\Eye / vision finding\Visual system disorder\Disorder of vision (disorder)\Color vision deficiency (disorder)\Congenital color blindness
\Eye / vision finding\Visual system disorder\Disorder of vision (disorder)\Visual disturbance (disorder)\Colour blindness\Congenital color blindness

\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
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital color blindness
\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
\Disease\Disorder of body system\Visual system disorder\Disorder of vision (disorder)\Color vision deficiency (disorder)\Congenital color blindness
\Disease\Disorder of body system\Visual system disorder\Disorder of vision (disorder)\Visual disturbance (disorder)\Colour blindness\Congenital color blindness
\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

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
Congenital color blindness	Is a	Color vision deficiency (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital color blindness	Is a	Colour blindness	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital color blindness	Finding site	Retinal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital color blindness	Is a	Congenital anomaly of eye	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital color blindness	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital color blindness	Is a	Congenital disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital color blindness	Has interpretation	Abnormal	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital color blindness	Interprets	Vision observable (observable entity)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital color blindness	Interprets	Visual function (observable entity)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital color blindness	Has interpretation	Abnormal	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital color blindness	Interprets	Visual function (observable entity)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital color blindness	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital color blindness	Finding site	Retinal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Protan defect	Is a	True	Congenital color blindness	Inferred relationship	Existential restriction modifier (core metadata concept)
Tritan defect (disorder)	Is a	True	Congenital color blindness	Inferred relationship	Existential restriction modifier (core metadata concept)
Achromatopsia	Is a	True	Congenital color blindness	Inferred relationship	Existential restriction modifier (core metadata concept)
Deutan defect	Is a	True	Congenital color blindness	Inferred relationship	Existential restriction modifier (core metadata concept)
Blue cone monochromatism (disorder)	Is a	True	Congenital color blindness	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
347840013	Congenital color blindness	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
347841012	Congenital colour blindness	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
620175012	Congenital color blindness (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
347840013	Congenital color blindness	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
347840013	Congenital color blindness	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
347841012	Congenital colour blindness	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
347841012	Congenital colour blindness	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
620175012	Congenital color blindness (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
620175012	Congenital color blindness (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
393771000274115	Angeborene Farbenblindheit	de	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
445081000274119	Angeborene Achromatopsie	de	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
545331000274112	Kongenitale Farbenblindheit	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
76901000077113	achromatopsie congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
76901000077113	achromatopsie congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
393771000274115	Angeborene Farbenblindheit	de	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
445081000274119	Angeborene Achromatopsie	de	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
545331000274112	Kongenitale Farbenblindheit	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module