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421455009: Episodic ataxia (disorder)

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

9 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Episodic ataxia (disorder) Is a Hereditary disorder of nervous system false Inferred relationship Some
Episodic ataxia (disorder) Is a Autosomal dominant hereditary disorder (disorder) true Inferred relationship Some
Episodic ataxia (disorder) Is a Cerebellar ataxia false Inferred relationship Some
Episodic ataxia (disorder) Finding site Cerebellar structure false Inferred relationship Some 1
Episodic ataxia (disorder) Associated morphology dégénérescence false Inferred relationship Some 1
Episodic ataxia (disorder) Finding site Cerebellar structure false Inferred relationship Some
Episodic ataxia (disorder) Associated morphology dégénérescence false Inferred relationship Some 1
Episodic ataxia (disorder) Is a Hereditary cerebellar degeneration false Inferred relationship Some
Episodic ataxia (disorder) Is a Hereditary ataxia (disorder) true Inferred relationship Some
Episodic ataxia (disorder) Finding site Structure of nervous system (body structure) true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Marie's cerebellar ataxia Is a True Episodic ataxia (disorder) Inferred relationship Some
Episodic ataxia type 1 (disorder) Is a True Episodic ataxia (disorder) Inferred relationship Some
Episodic ataxia type 2 (disorder) Is a True Episodic ataxia (disorder) Inferred relationship Some
Episodic ataxia type 7 (EA7) is an exceedingly rare form of hereditary episodic ataxia characterized by ataxia with weakness, vertigo, and dysarthria without interictal findings. Is a True Episodic ataxia (disorder) Inferred relationship Some
Episodic ataxia type 6 (EA6) is an exceedingly rare form of hereditary episodic ataxia with varying degrees of ataxia and associated findings including slurred speech, headache, confusion and hemiplegia. Is a True Episodic ataxia (disorder) Inferred relationship Some
A rare form of hereditary episodic ataxia characterized by late-onset episodic ataxia, recurrent attacks of vertigo, and diplopia. Is a True Episodic ataxia (disorder) Inferred relationship Some
A rare form of hereditary episodic ataxia characterized by vestibular ataxia, vertigo, tinnitus, and interictal myokymia. Is a True Episodic ataxia (disorder) Inferred relationship Some
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. Is a True Episodic ataxia (disorder) Inferred relationship Some
Episodic ataxia with slurred speech is a rare hereditary ataxia characterized by recurrent episodes of ataxia with variable frequency and duration, associated with slurred speech, generalized muscle weakness and balance disturbance. Other symptoms may occur between episodes, including intention tremor, gait ataxia, mild dysarthria, myokymia, migraine and nystagmus. Is a True Episodic ataxia (disorder) Inferred relationship Some

This concept is not in any reference sets

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