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Echinobase
Summary Literature (0)
DOID:0050960 - spinocerebellar ataxia type 10

Disease Ontology Definition:An autosomal dominant cerebellar ataxia that is characterized by gait ataxia, upper-limb ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the ATXN10 gene.

Synonyms:

Echinobase Genes : atxn10


MIM:
MIM:603516 - spinocerebellar ataxia 10; sca10

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

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