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spinocerebellar ataxia, autosomal recessive 24

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

Any autosomal dominant cerebellar ataxia in which the cause of the disease is a mutation in the UBA5 gene.

Synonyms

  • SCAR24
  • UBA5 autosomal dominant cerebellar ataxia
  • autosomal dominant cerebellar ataxia caused by mutation in UBA5
  • spinocerebellar ataxia, autosomal recessive 24
  • spinocerebellar ataxia, autosomal recessive 24; SCAR24
  • spinocerebellar ataxia, autosomal recessive type 24
OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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