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Summary Literature (0)
DOID:0050980 - spinocerebellar ataxia type 31

Disease Ontology Definition:An autosomal dominant cerebellar ataxia that is characterized by late-onset ataxia, dysarthria and horizontal nystagmus, has_material_basis_in repeat expansion mutation in the BEAN1 gene.

Synonyms:

Xenbase Genes : plekhg4

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007296 - spinocerebellar ataxia type 31


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)