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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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Autosomal genetic disease
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Autosomal recessive disease
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Autosomal recessive cerebellar ataxia
Spinocerebellar ataxia, autosomal recessive 27
rare
Identifiers
MONDO:0032706
OMIM:618369
Causal genes
GDAP2
Part of
Autosomal recessive cerebellar ataxia
Also known as
SCAR27
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