2. Dubin Johnson Syndrome
Dubin Johnson Syndrome is a rare genetic liver disorder that tends to affect people of Middle Eastern Jewish heritage disproportionately to other groups. It appears to be associated with clotting factor VII in this population. Symptoms may include.....
Healthline.com (OMS Preferred Provider)

3. Dubin-Johnson syndrome - Genetics Home Reference
Dubin-Johnson syndrome is a condition characterized by jaundice, which is a yellowing of the skin and whites of the eyes. In most affected people jaundice appears during adolescence or early adulthood, although a few individuals have been diagnose.....
MedlinePlus (Offsite)

4. Dubin-Johnson syndrome - References - Genetics Home Reference
Keitel V, Nies AT, Brom M, Hummel-Eisenbeiss J, Spring H, Keppler D. A common Dubin-Johnson syndrome mutation impairs protein maturation and transport activity of MRP2 (ABCC2). Am J Physiol Gastrointest Liver Physiol. 2003 Jan;284(1):G165-74. Epub.....
MedlinePlus (Offsite)

5. Dubin-Johnson syndrome
Dubin-Johnson syndrome is a disorder passed down through families (inherited) in which a person has mild jaundice throughout life.
www.uhseast.com

6. Treatment of Dubin-Johnson Syndrome
Dubin-Johnson sydrome is a rare liver disorder characterized by mild jaundice throughout life. It is caused by an incomplete processing of bilirubin, a product of the liver's metabolism of worn-out red blood cells normally sent into the digestive ...
www.mayoclinic.org

7. Dubin-Johnson Syndrome: eMedicine Gastroenterology
Dubin-Johnson syndrome (DJS) is a type of hereditary hyperbilirubinemia that was first described independently in 1954 by Dubin and Johnson and by Sprinz and Nelson.
emedicine.medscape.com

8. Dubin-Johnson Syndrome Symptoms & Treatment
Dubin-Johnson syndrome is a very rare genetic disorder. In order to inherit the condition, a child must get a copy of the defective gene from both parents.
www.christusschumpert.org

9. Dubin-Johnson syndrome, and Rotor syndrome
Dubin-Johnson syndrome, and Rotor syndrome
healthinsite.gov.au

10. Ocular Syndromes and Systemic Diseases: Dubin-Johnson Syndrome
General: Onset in infancy, but may be present at birth; autosomal dominant; liver cells are unable to excrete conjugated bilirubin; manifestations similar to Rotor syndrome, except that in the latter there is no melanin pigment present in the live...
www.medrounds.org