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Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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RNU12-related minor spliceopathy disorder
Spinocerebellar ataxia, autosomal recessive 33
rare
Identifiers
MONDO:0859360
OMIM:620208
Part of
RNU12-related minor spliceopathy disorder
Autosomal recessive cerebellar ataxia
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