46808003: Marie's cerebellar ataxia (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding related to coordination / incoordination\Ataxia\Hereditary ataxia\Episodic ataxia\Marie's cerebellar ataxia
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary ataxia\Episodic ataxia\Marie's cerebellar ataxia
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Episodic ataxia\Marie's cerebellar ataxia
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary ataxia\Episodic ataxia\Marie's cerebellar ataxia
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary ataxia\Episodic ataxia\Marie's cerebellar ataxia

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2837795011	Marie cerebellar ataxia	en	Synonym	Active	Case sensitive	SNOMED CT core
78021014	Marie's cerebellar ataxia	en	Synonym	Active	Case sensitive	SNOMED CT core
78022019	Hereditary cerebellar ataxia	en	Synonym	Active	Case insensitive	SNOMED CT core
784198019	Marie's cerebellar ataxia (disorder)	en	Fully specified name	Active	Case sensitive	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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