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Summary Literature (0)
MIM:616354 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20

Xenbase Genes: snx14

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014601 - autosomal recessive spinocerebellar ataxia 20

Disease Ontology (DO):
DOID:0080066 - autosomal recessive spinocerebellar ataxia 20