718752007: Episodic ataxia type 7 (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding related to coordination / incoordination\Ataxia\...
• \Hereditary ataxia\Episodic ataxia\Episodic ataxia type 7
• \Cerebellar ataxia\Episodic ataxia type 7
• \Central nervous system finding\Finding of brain\Encephalopathy\Cerebellar disorder\Cerebellar ataxia\Episodic ataxia type 7
• \Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Cerebellar disorder\Cerebellar ataxia\Episodic ataxia type 7
• \Finding of head and neck region\Head finding\...
• \Finding of brain\Encephalopathy\Cerebellar disorder\Cerebellar ataxia\Episodic ataxia type 7
• \Disorder of head\Encephalopathy\Cerebellar disorder\Cerebellar ataxia\Episodic ataxia type 7
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary ataxia\Episodic ataxia\Episodic ataxia type 7
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Episodic ataxia\Episodic ataxia type 7
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary ataxia\Episodic ataxia\Episodic ataxia type 7
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary ataxia\Episodic ataxia\Episodic ataxia type 7
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Cerebellar disorder\Cerebellar ataxia\Episodic ataxia type 7
• \Disease\Disorder of head\Encephalopathy\Cerebellar disorder\Cerebellar ataxia\Episodic ataxia type 7

Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3313730018	Episodic ataxia type 7 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3313731019	Episodic ataxia type 7	en	Synonym	Active	Case insensitive	SNOMED CT core
3313732014	An exceedingly rare form of hereditary episodic ataxia with characteristics of ataxia with weakness, vertigo, and dysarthria without interictal findings.	en	Definition	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

Back to Start