Ornithine translocase deficiency syndrome
Other Names for this Disease
- Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
- HHH syndrome
- Ornithine translocase deficiency
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Tests & Diagnosis
- 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.
- 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.