Episodic ataxia type 5 - CACNB4 mutation (Q90148)
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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 |
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| 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
CID11:ID_2072072482
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dki-india-ID_2072072482
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Concluído
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13 August 2026
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