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Diseases

Genetic and Rare Diseases Information Center (GARD)

Gyrate atrophy of choroid and retina


Other Names for this Disease
  • Ornithine aminotransferase deficiency
  • Ornithine ketoacid aminotransferase deficiency
  • Gyrate atrophy
  • OAT deficiency
  • OKT deficiency
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Tests & Diagnosis

On this page

Testing

  • The Genetic Testing Registry (GTR) provides information about the genetic tests for this condition. The intended audience for the GTR is health care providers and researchers. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.
  • Orphanet lists international laboratories offering diagnostic testing for this condition.

Newborn Screening

  • The Newborn Screening Coding and Terminology Guide has information on the standard codes used for newborn screening tests. Using these standards helps compare data across different laboratories. This resource was created by the National Library of Medicine.
Other Names for this Disease
  • Ornithine aminotransferase deficiency
  • Ornithine ketoacid aminotransferase deficiency
  • Gyrate atrophy
  • OAT deficiency
  • OKT deficiency
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.