Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:616948 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22; SCAR22

Xenbase Genes: vwa3b

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014845 - spinocerebellar ataxia, autosomal recessive 22

Disease Ontology (DO):
DOID:0111614 - autosomal recessive spinocerebellar ataxia 22