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Summary Literature (0)
DOID:0050973 - spinocerebellar ataxia type 23

Disease Ontology Definition:An autosomal dominnant cerebellar ataxia that is characterized by slowly progressive ataxia, dysarthria, slow saccades and hyperreflexia, has_material_basis_in mutation in the PDYN gene.

Synonyms:

Xenbase Genes : pdyn

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012449 - spinocerebellar ataxia type 23


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)