232148006: achromatopsie congénitale (trouble)

SNOMED CT Concept\constatation clinique\...

\constatation à propos d'une région de la tête et du cou\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)\trouble rétinien (trouble)\Colour blindness\Congenital color blindness
\Finding of head region\constatation à propos d'un globe oculaire\Retina finding (finding)\trouble rétinien (trouble)\Colour blindness\Congenital color blindness
\Finding of head region\constatation à propos d'un globe oculaire\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\trouble rétinien (trouble)\Colour blindness\Congenital color blindness

\affection de la tête\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\trouble rétinien (trouble)\Colour blindness\Congenital color blindness

\constatation à propos des yeux ou de la vue\constatation à propos d'un globe oculaire\Retina finding (finding)\trouble rétinien (trouble)\Colour blindness\Congenital color blindness
\constatation à propos des yeux ou de la vue\constatation à propos d'un globe oculaire\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\trouble rétinien (trouble)\Colour blindness\Congenital color blindness
\constatation à propos des yeux ou de la vue\affection du système visuel\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\trouble rétinien (trouble)\Colour blindness\Congenital color blindness
\constatation à propos des yeux ou de la vue\affection du système visuel\Disorder of vision\Colour vision deficiency\Congenital color blindness
\constatation à propos des yeux ou de la vue\affection du système visuel\Disorder of vision\Visual disturbance\Colour blindness\Congenital color blindness

\Disease\affection d'un système corporel\affection du système visuel\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\trouble rétinien (trouble)\Colour blindness\Congenital color blindness
\Disease\affection d'un système corporel\affection du système visuel\Disorder of vision\Colour vision deficiency\Congenital color blindness
\Disease\affection d'un système corporel\affection du système visuel\Disorder of vision\Visual disturbance\Colour blindness\Congenital color blindness
\Disease\affection de la tête\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\trouble rétinien (trouble)\Colour blindness\Congenital color blindness
\Disease\Congenital disease\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

699421000077119 achromatopsie congénitale (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

76901000077113 achromatopsie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital color blindness	est un(e) (attribut)	Congenital anomaly of eye	false	Inferred relationship	Some
Congenital color blindness	survenue (attribut)	congénital	false	Inferred relationship	Some
Congenital color blindness	est un(e) (attribut)	Congenital disease	true	Inferred relationship	Some
Congenital color blindness	a pour interprétation (attribut)	anormal	false	Inferred relationship	Some	1
Congenital color blindness	interprète (attribut)	entité observable de la vision	false	Inferred relationship	Some	1
Congenital color blindness	interprète (attribut)	Visual function (observable entity)	false	Inferred relationship	Some	1
Congenital color blindness	a pour interprétation (attribut)	anormal	false	Inferred relationship	Some	1
Congenital color blindness	interprète (attribut)	Visual function (observable entity)	false	Inferred relationship	Some	1
Congenital color blindness	est un(e) (attribut)	Colour vision deficiency	true	Inferred relationship	Some
Congenital color blindness	est un(e) (attribut)	Colour blindness	true	Inferred relationship	Some
Congenital color blindness	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Congenital color blindness	localisation d'une constatation (attribut)	structure de la rétine	true	Inferred relationship	Some	1
Congenital color blindness	localisation d'une constatation (attribut)	structure de la rétine	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Blue cone monochromatism (disorder)	est un(e) (attribut)	True	Congenital color blindness	Inferred relationship	Some
Protan defect (disorder)	est un(e) (attribut)	True	Congenital color blindness	Inferred relationship	Some
Tritan defect (disorder)	est un(e) (attribut)	True	Congenital color blindness	Inferred relationship	Some
achromatopsie (trouble)	est un(e) (attribut)	True	Congenital color blindness	Inferred relationship	Some
Deutan defect	est un(e) (attribut)	True	Congenital color blindness	Inferred relationship	Some

This concept is not in any reference sets