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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Gilbert syndrome

*

* Not a rare disease

Other Names for this Disease

  • Cholemia, familial
  • Gilbert's disease
  • Hyperbilirubinemia Arias type
  • Hyperbilirubinemia type 1
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Your Question

What are the symptoms of Gilbert syndrome?

Our Answer

We have identified the following information that we hope you find helpful. If you still have questions, please contact us.

What is Gilbert syndrome?

Gilbert syndrome is a common, mild liver disorder in which the liver doesn't properly process bilirubin, a substance produced by the breakdown of red blood cells. Gilbert syndrome typically doesn't require treatment or pose serious complications. In fact, Gilbert syndrome is usually not considered a disease because of its benign nature. Many individuals find out they have the disorder by accident, when they have a blood test that shows elevated bilirubin levels. More males than females have been diagnosed with Gilbert syndrome.[1] This condition is caused by mutations in the UGT1A1 gene and is inherited in an autosomal recessive pattern.[2]
Last updated: 5/2/2011

What are the signs and symptoms of Gilbert syndrome?

While many people with Gilbert syndrome never experience any symptoms,  mild jaundice may occur if bilirubin levels get high enough. Other possible symptoms may include fatigue, weakness and abdominal pain.[1][3]  
Last updated: 5/2/2011

References
Other Names for this Disease
  • Cholemia, familial
  • Gilbert's disease
  • Hyperbilirubinemia Arias type
  • Hyperbilirubinemia type 1
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.