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Episodic ataxia type 7
Disease definition
Episodic ataxia type 7 (EA7) is an exceedingly rare form of Hereditary episodic ataxia (see this term) characterized by ataxia with weakness, vertigo, and dysarthria without interictal findings.
ORPHA:209970
Classification level: Disorder- Synonym(s): -
- Prevalence: <1 / 1 000 000
- Inheritance: Autosomal dominant
- Age of onset: Childhood
- ICD-10: G11.8
- OMIM: 611907
- UMLS: C2677843
- 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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