405809000: Ocular motor apraxia Cogan type (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Eye / vision finding\Visual system disorder\...
• \Hereditary disorder of the visual system\Oculomotor apraxia - Cogan type
• \Congenital anomaly of visual system\Oculomotor apraxia - Cogan type
• \Disorder of eye movements\Strabismus\Oculomotor apraxia\Oculomotor apraxia - Cogan type
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the visual system\Oculomotor apraxia - Cogan type
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Oculomotor apraxia - Cogan type
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Oculomotor apraxia - Cogan type
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the visual system\Oculomotor apraxia - Cogan type
• \Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system\Oculomotor apraxia - Cogan type
• \Disease\Disorder of body system\Visual system disorder\Congenital anomaly of visual system\Oculomotor apraxia - Cogan type
• \Disease\Disorder of body system\Visual system disorder\Disorder of eye movements\Strabismus\Oculomotor apraxia\Oculomotor apraxia - Cogan type
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of visual system\Oculomotor apraxia - Cogan type
• \Disease\Developmental disorder\Developmental hereditary disorder\Oculomotor apraxia - Cogan type
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of visual system\Oculomotor apraxia - Cogan type

Status: current, Primitive. Date: 31-Jan 2004. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2149639013	Oculomotor apraxia - Cogan type (disorder)	en	Fully specified name	Inactive	Initial character case insensitive	SNOMED CT core
2157583012	Oculomotor apraxia - Cogan type	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
5045004019	Ocular motor apraxia Cogan type (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
5045005018	Ocular motor apraxia Cogan type	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
5045006017	Congenital saccade initiation failure	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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