405809000: apraxie oculomotrice type Cogan (trouble)

SNOMED CT Concept\constatation clinique\...

\constatation à propos des yeux ou de la vue\affection du système visuel\...

\Hereditary disorder of the visual system\Ocular motor apraxia Cogan type (disorder)

\Congenital anomaly of visual system\Ocular motor apraxia Cogan type (disorder)

\Disorder of eye movements\Strabismus\Oculomotor apraxia (disorder)\Ocular motor apraxia Cogan type (disorder)

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of the visual system\Ocular motor apraxia Cogan type (disorder)
\Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\Ocular motor apraxia Cogan type (disorder)
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Ocular motor apraxia Cogan type (disorder)
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of the visual system\Ocular motor apraxia Cogan type (disorder)
\Disease\affection d'un système corporel\affection du système visuel\Hereditary disorder of the visual system\Ocular motor apraxia Cogan type (disorder)
\Disease\affection d'un système corporel\affection du système visuel\Congenital anomaly of visual system\Ocular motor apraxia Cogan type (disorder)
\Disease\affection d'un système corporel\affection du système visuel\Disorder of eye movements\Strabismus\Oculomotor apraxia (disorder)\Ocular motor apraxia Cogan type (disorder)
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of visual system\Ocular motor apraxia Cogan type (disorder)
\Disease\trouble du développement\Developmental hereditary disorder\Ocular motor apraxia Cogan type (disorder)
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of visual system\Ocular motor apraxia Cogan type (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2004. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Ocular motor apraxia Cogan type (disorder)	est un(e) (attribut)	Hereditary disorder of the visual system	true	Inferred relationship	Some
Ocular motor apraxia Cogan type (disorder)	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Ocular motor apraxia Cogan type (disorder)	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Ocular motor apraxia Cogan type (disorder)	est un(e) (attribut)	Congenital anomaly of visual system	true	Inferred relationship	Some
Ocular motor apraxia Cogan type (disorder)	est un(e) (attribut)	Developmental hereditary disorder	true	Inferred relationship	Some
Ocular motor apraxia Cogan type (disorder)	morphologie associée (attribut)	structure anormale sur le plan morphologique	true	Inferred relationship	Some	1
Ocular motor apraxia Cogan type (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Ocular motor apraxia Cogan type (disorder)	est un(e) (attribut)	Oculomotor apraxia (disorder)	true	Inferred relationship	Some
Ocular motor apraxia Cogan type (disorder)	localisation d'une constatation (attribut)	Eye region structure (body structure)	false	Inferred relationship	Some	1
Ocular motor apraxia Cogan type (disorder)	morphologie associée (attribut)	Misalignment (morphologic abnormality)	false	Inferred relationship	Some	1
Ocular motor apraxia Cogan type (disorder)	interprète (attribut)	Ocular muscle balance	false	Inferred relationship	Some	1
Ocular motor apraxia Cogan type (disorder)	localisation d'une constatation (attribut)	Structure of visual system (body structure)	true	Inferred relationship	Some	1
Ocular motor apraxia Cogan type (disorder)	interprète (attribut)	Ocular motility observable	false	Inferred relationship	Some
Ocular motor apraxia Cogan type (disorder)	a pour interprétation (attribut)	anormal	false	Inferred relationship	Some	1
Ocular motor apraxia Cogan type (disorder)	interprète (attribut)	Ocular muscle balance	false	Inferred relationship	Some	1
Ocular motor apraxia Cogan type (disorder)	a pour interprétation (attribut)	anormal	false	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Cortical paralysis of fixation syndrome	est un(e) (attribut)	False	Ocular motor apraxia Cogan type (disorder)	Inferred relationship	Some

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2157583012	Oculomotor apraxia - Cogan type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5045004019	Ocular motor apraxia Cogan type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5045005018	Ocular motor apraxia Cogan type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5045006017	Congenital saccade initiation failure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
638091000241111	apraxie oculomotrice type Cogan (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
968381000172111	apraxie oculomotrice type Cogan	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)