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Summary Literature (0)
DOID:0050956 - spinocerebellar ataxia type 6

Disease Ontology Definition:An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, has_material_basis_in mutation in the CACNA1A gene.

Synonyms:

Xenbase Genes : cacna1a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008457 - spinocerebellar ataxia type 6


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)