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Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Hereditary dementia
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Autosomal dominant cerebellar ataxia
Spinocerebellar ataxia 9
rare
Identifiers
MONDO:0013029
OMIM:612876
Part of
Autosomal dominant cerebellar ataxia
Also known as
cerebellar ataxia type 9 · SCA9 · spinocerebellar ataxia type 9
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