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Summary Literature (0)
DOID:0050985 - spinocerebellar ataxia type 38

Disease Ontology Definition:An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia and nystagmus, presenting in mid-adulthood, and has_material_basis_in mutation to the ELOVL5 gene.

Synonyms:

Xenbase Genes : elovl5

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014417 - spinocerebellar ataxia type 38


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)