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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Spinocerebellar ataxia 25


Other Names for this Disease
  • SCA25
  • Spinocerebellar ataxia type 25
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Overview


These Web pages are updated as the Genetic and Rare Diseases Information Center receives questions and as new information becomes available. If you don’t see many information resources on this page, it may be because the Information Center hasn’t yet received a question about this condition.

Your Questions Answered
by the Genetic and Rare Diseases Information Center

Please contact us with your questions about Spinocerebellar ataxia 25. We will answer your question and update these pages with new resources and information.

Basic Information

In Depth Information

  • The Online Mendelian Inheritance in Man (OMIM) is an catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. 
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs.  Access to this database is free of charge.
  • PubMed is a searchable database of medical literature and lists journal articles that discuss Spinocerebellar ataxia 25. Click on the link to view a sample search on this topic.

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