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Diseases

Genetic and Rare Diseases Information Center (GARD)

Spinocerebellar ataxia 7


Other Names for this Disease
  • SCA7
  • Spinocerebellar ataxia type 7
  • Olivopontocerebellar atrophy 3
  • OPCA3
  • Autosomal dominant cerebellar ataxia type 2
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Research

Clinical Trials & Research for this Disease

  • ClinicalTrials.gov lists trials that are studying or have studied Spinocerebellar ataxia 7. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.
  • The Research Portfolio Online Reporting Tool (RePORT) provides access to reports, data, and analyses of research activities at the National Institutes of Health (NIH), including information on NIH expenditures and the results of NIH-supported research. Although these projects may not conduct studies on humans, you may want to contact the investigators to learn more. To search for studies, enter the disease name in the "Text Search" box. Then click "Submit Query".

Patient Registry

  • Coordination of Rare Diseases at Sanford (CoRDS) hosts a specific registry for patients with ataxia in partnership with the National Ataxia Foundation. The goal of the CoRDS registry is to connect as many patients and researchers as possible to help advance treatments and cures for rare diseases. The CoRDS registry is free for patients to enroll and for researchers to access.
Other Names for this Disease
  • SCA7
  • Spinocerebellar ataxia type 7
  • Olivopontocerebellar atrophy 3
  • OPCA3
  • Autosomal dominant cerebellar ataxia type 2
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.