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Disease Ontology Browser
autosomal recessive spinocerebellar ataxia 17 (DOID:0080064)
Alliance: disease page
Synonyms: SCAR17
Alt IDs: OMIM:616127
Definition: An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the CWF19L1 gene on chromosome 10q24.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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04/16/2024
MGI 6.23 		The Jackson Laboratory