405809000: Ocular motor apraxia Cogan type (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Eye / vision finding\Visual system disorder\...
• \Hereditary disorder of the visual system (disorder)\Ocular motor apraxia Cogan type (disorder)
• \Congenital anomaly of visual system\Ocular motor apraxia Cogan type (disorder)
• \Disorder of eye movements\Strabismus\Oculomotor apraxia\Ocular motor apraxia Cogan type (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the visual system (disorder)\Ocular motor apraxia Cogan type (disorder)
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Ocular motor apraxia Cogan type (disorder)
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Ocular motor apraxia Cogan type (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of visual system\Ocular motor apraxia Cogan type (disorder)
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the visual system (disorder)\Ocular motor apraxia Cogan type (disorder)
• \Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system (disorder)\Ocular motor apraxia Cogan type (disorder)
• \Disease\Disorder of body system\Visual system disorder\Congenital anomaly of visual system\Ocular motor apraxia Cogan type (disorder)
• \Disease\Disorder of body system\Visual system disorder\Disorder of eye movements\Strabismus\Oculomotor apraxia\Ocular motor apraxia Cogan type (disorder)
• \Disease\Developmental disorder\Developmental hereditary disorder\Ocular motor apraxia Cogan type (disorder)
• \Disease\Developmental disorder\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:

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

Expanded Value Set

Reference Sets

GB English

US English

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