232148006: Congenital color blindness (disorder)

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

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

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

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

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

1835281000195119 cecità ai colori congenita it 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

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

Expanded Value Set

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

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

This concept is not in any reference sets