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GTR Home > Conditions/Phenotypes > Spinocerebellar ataxia, autosomal recessive 22

Spinocerebellar ataxia, autosomal recessive 22

Summary

Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the VWA3B gene. [from MONDO]

Available tests

4 tests are in the database for this condition.

Clinical tests (4 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: SCAR22, VWA3B
    Summary: von Willebrand factor A domain containing 3B

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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