autosomal recessive spinocerebellar ataxia 15

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Summary

Literature (0)

DOID:0080057 - autosomal recessive spinocerebellar ataxia 15

Disease Ontology Definition:An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the RUBCN gene on chromosome 3q29.

Synonyms: SCAR15,

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

: rubcn

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014311 - autosomal recessive spinocerebellar ataxia 15

MONDO:0014311 - autosomal recessive spinocerebellar ataxia 15

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)