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Summary Literature (0)
DOID:0050984 - spinocerebellar ataxia type 37

Disease Ontology Definition:An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia and dysarthria, presenting in mid-adulthood, and has_material_basis_in mutation to the DAB1 gene.

Synonyms:

Xenbase Genes : dab1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014410 - spinocerebellar ataxia type 37


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)