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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
Spinocerebellar ataxia 44
rare
Identifiers
MONDO:0033479
OMIM:617691
Orphanet:631095
Causal genes
GRM1
Part of
Autosomal dominant cerebellar ataxia
Also known as
SCA44
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