autosomal recessive spinocerebellar ataxia 26

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: xrcc1

MIM:

MIM:617633 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26

MIM:617633 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26

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)