Episodic ataxia type 5 - CACNB4 mutation (Q90148): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed label, description and/or aliases in pt-br, en
‎Changed an Item
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/2072072482 / rank
 
Normal rank

Revision as of 17:05, 15 August 2026

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.
Language Label Description Also known as
default for all languages
ID_2072072482
    English
    Episodic ataxia type 5 - CACNB4 mutation
    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.

      Statements