autosomal recessive spinocerebellar ataxia 10

Summary

DOID:0050999 - autosomal recessive spinocerebellar ataxia 10

Disease Ontology Definition:An autosomal recessive cerebellar ataxia that is characterized by ataxia, dysarthria, nystagmus and marked cerebellar atrophy, has_material_basis_in mutation in the ANO10 gene.

Synonyms: SCAR10

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

: ano10

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013392 - autosomal recessive spinocerebellar ataxia 10

MONDO:0013392 - autosomal recessive spinocerebellar ataxia 10

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)