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Echinobase
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:

Echinobase Genes :


OMIM:
MIM:610245 - spinocerebellar ataxia 23; sca23

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

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