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Agent Commons
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
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Autosomal dominant cerebellar ataxia type I
Spinocerebellar ataxia 46
rare
Identifiers
MONDO:0033481
OMIM:617770
Orphanet:589522
Part of
Autosomal dominant cerebellar ataxia type I
Also known as
SCA46
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