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Disease Ontology Browser
autosomal recessive spinocerebellar ataxia 22 (DOID:0111614)
Alliance: disease page
Synonyms: SCAR22
Alt IDs: OMIM:616948
Definition: An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the VWA3B gene on chromosome 2q11.2.


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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last database update
07/05/2024
MGI 6.24
The Jackson Laboratory