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:615386 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14; SCAR14

Xenbase Genes: sptbn2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014159 - autosomal recessive spinocerebellar ataxia 14

Disease Ontology (DO):
DOID:0080058 - autosomal recessive spinocerebellar ataxia 14