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Summary Literature (0)
DOID:0050957 - spinocerebellar ataxia type 4

Disease Ontology Definition:An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria and peripheral neuropathy, has_material_basis_in mutation in the SCA4 gene.

Synonyms:

Xenbase Genes : plekhg4

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010847 - ulna pre-cartilage condensation

MIM:
MIM:600223 - SPINOCEREBELLAR ATAXIA 4; SCA4

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)