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Summary Literature (0)
MIM:616949 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23; SCAR23

Xenbase Genes: tdp2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014846 - spinocerebellar ataxia, autosomal recessive 23

Disease Ontology (DO):
DOID:0111613 - autosomal recessive spinocerebellar ataxia 23