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Episodic ataxia type 3
Disease definition
Episodic ataxia type 3 (EA3) is a very rare form of Hereditary episodic ataxia (see this term) characterized by vestibular ataxia, vertigo, tinnitus, and interictal myokymia.
ORPHA:79135
Classification level: Disorder- Synonym(s):
- Episodic ataxia-vertigo-tinnitus-myokymia syndrome
- Prevalence: <1 / 1 000 000
- Inheritance: Autosomal dominant
- Age of onset: All ages
- ICD-10: G11.8
- OMIM: 606554
- UMLS: C1847839
- MeSH: -
- GARD: -
- MedDRA: -
Detailed information
Professionals
- Summary information
- Japanese (2019, pdf)
- Clinical genetics review
- English (2022)
Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
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