SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17

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Summary

Literature (0)

MIM:616127 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17

Xenbase Genes: cwf19l1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014503 - proximal phalanx of digit 3

MONDO:0014503 - proximal phalanx of digit 3

Disease Ontology (DO):

DOID:0080064 - autosomal recessive spinocerebellar ataxia 17

DOID:0080064 - autosomal recessive spinocerebellar ataxia 17