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Summary Literature (0)
DOID:0080260 - autosomal recessive spinocerebellar ataxia 26

Disease Ontology Definition:An autosomal recessive cerebellar ataxia that has_material_basis_in compound heterozygous mutation in the XRCC1 gene on chromosome 19q13.

Synonyms: SCAR26,

Xenbase Genes : xrcc1

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive cerebellar ataxia (is_a)