421455009: Episodic ataxia (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of coordination\Ataxia\Hereditary ataxia (disorder)\Episodic ataxia

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary ataxia (disorder)\Episodic ataxia
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Episodic ataxia
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary ataxia (disorder)\Episodic ataxia
\Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary ataxia (disorder)\Episodic ataxia

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2006. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2615430011 Episodic ataxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2618099018 Episodic ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2615430011 Episodic ataxia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2615430011 Episodic ataxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2618099018 Episodic ataxia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2618099018 Episodic ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5290321000241117 ataxie épisodique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5290321000241117 ataxie épisodique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Episodic ataxia	Is a	Hereditary disorder of nervous system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Episodic ataxia	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Episodic ataxia	Is a	Cerebellar ataxia	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Episodic ataxia	Finding site	Cerebellar structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Episodic ataxia	Associated morphology	dégénérescence	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Episodic ataxia	Finding site	Cerebellar structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Episodic ataxia	Associated morphology	dégénérescence	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Episodic ataxia	Is a	Hereditary cerebellar degeneration	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Episodic ataxia	Is a	Hereditary ataxia (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Episodic ataxia	Finding site	Nervous system structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Marie's cerebellar ataxia	Is a	True	Episodic ataxia	Inferred relationship	Existential restriction modifier (core metadata concept)
Episodic ataxia type 1 (disorder)	Is a	True	Episodic ataxia	Inferred relationship	Existential restriction modifier (core metadata concept)
Episodic ataxia type 2 (disorder)	Is a	True	Episodic ataxia	Inferred relationship	Existential restriction modifier (core metadata concept)
Episodic ataxia type 7 (disorder)	Is a	True	Episodic ataxia	Inferred relationship	Existential restriction modifier (core metadata concept)
Episodic ataxia type 6 (disorder)	Is a	True	Episodic ataxia	Inferred relationship	Existential restriction modifier (core metadata concept)
Episodic ataxia type 4 (disorder)	Is a	True	Episodic ataxia	Inferred relationship	Existential restriction modifier (core metadata concept)
Episodic ataxia type 3 (disorder)	Is a	True	Episodic ataxia	Inferred relationship	Existential restriction modifier (core metadata concept)
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.	Is a	True	Episodic ataxia	Inferred relationship	Existential restriction modifier (core metadata concept)
Episodic ataxia with slurred speech (disorder)	Is a	True	Episodic ataxia	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets