718756005: Episodic ataxia type 5 (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Head finding (finding)\Finding of brain\Disorder of brain\Cerebellar disorder\Cerebellar ataxia\Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.
• \Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Cerebellar disorder\Cerebellar ataxia\Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.
• \Finding of coordination\Ataxia\...
• \Hereditary ataxia (disorder)\Episodic ataxia\Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.
• \Cerebellar ataxia\Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.
• \Central nervous system finding\Finding of brain\Disorder of brain\Cerebellar disorder\Cerebellar ataxia\Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.
• \Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Cerebellar disorder\Cerebellar ataxia\Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary ataxia (disorder)\Episodic ataxia\Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Episodic ataxia\Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.
• \Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary ataxia (disorder)\Episodic ataxia\Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary ataxia (disorder)\Episodic ataxia\Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Cerebellar disorder\Cerebellar ataxia\Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.
• \Disease\Disorder of head (disorder)\Disorder of brain\Cerebellar disorder\Cerebellar ataxia\Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3313749019	Episodic ataxia type 5 (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3313750019	Episodic ataxia type 5	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5401854019	Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterized by recurrent episodes of vertigo and ataxia lasting several hours.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401855018	Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3313749019	Episodic ataxia type 5 (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3313749019	Episodic ataxia type 5 (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3313750019	Episodic ataxia type 5	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3313750019	Episodic ataxia type 5	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3313751015	An extremely rare form of hereditary episodic ataxia with characteristics of recurrent episodes of vertigo and ataxia lasting several hours.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401854019	Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterized by recurrent episodes of vertigo and ataxia lasting several hours.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401855018	Episodic ataxia type 5 (EA5) is an extremely rare form of hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3427191001000114	Ataxie, episodische, Typ 5	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
899791000172110	ataxie épisodique type 5	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
899791000172110	ataxie épisodique type 5	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3427191001000114	Ataxie, episodische, Typ 5	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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