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DOID:0050962 - spinocerebellar ataxia type 12
Disease Ontology Definition:An autosomal dominant cerebellar ataxia that is characterized by minor ataxia and intention tremor, has_material_basis_in CAG expansion of the PPP2R2B gene.
Synonyms:
Xenbase Genes : ppp2r2b
MONDO:0011439 - spinocerebellar ataxia type 12 |
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)