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Summary Literature (0)
DOID:0080064 - autosomal recessive spinocerebellar ataxia 17

Disease Ontology Definition:An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the CWF19L1 gene on chromosome 10q24.

Synonyms: SCAR17,

Xenbase Genes : cwf19l1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014503 - autosomal recessive spinocerebellar ataxia 17


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

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