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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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Huntington disease-like syndrome
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Spinocerebellar ataxia type 2
Spinocerebellar degeneration with slow eye movements
rare
Identifiers
MONDO:0010065
OMIM:271322
Part of
Spinocerebellar ataxia type 2
Also known as
SDSEM
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