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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
Cerebelloparenchymal disorder
Identifiers
MONDO:0000114
Part of
Hereditary disease
Subtypes
All diseases
Rare only
Disease
Myoclonic cerebellar dyssynergia
MONDO:0008945
Spinocerebellar ataxia type 17
MONDO:0011781
TBP
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