It can be differentiated from Dubin-Johnson syndrome in the following ways:

It is a distinct disorder, yet similar to Dubin-Johnson syndrome - both diseases cause an increase in conjugated bilirubin.

Rotor syndrome has many things in common with Dubin-Johnson syndrome, an exception being that the liver cells are not pigmented.

Dubin-Johnson syndrome and Rotor syndrome, which are rarer autosomal recessive disorders that are characterized by an increase of conjugated bilirubin.

These two types, along with Gilbert's syndrome, Dubin-Johnson syndrome, and Rotor syndrome, make up the five known hereditary defects in bilirubin metabolism.

Several different mutations in this gene have been observed in patients with Dubin-Johnson syndrome (DJS), an autosomal recessive disorder characterized by conjugated hyperbilirubinemia.

Defects in CMOAT (MRP2) results in Dubin-Johnson Syndrome and elevations of conjugated bilirubin.

Dubin-Johnson syndrome is an autosomal recessive disorder that causes an increase of conjugated bilirubin in the serum without elevation of liver enzymes (ALT, AST).

His publications include Spirometry in Tropical Pulmonary Eosinophilia and A Case of Congenital Hyperbilirubinaemia (Dubin-Johnson Syndrome) in Pakistan.

Bile duct obstruction Cirrhosis Dubin-Johnson syndrome (very rare) Hepatitis Intrahepatic cholestasis (buildup of bile in the liver) of many causes Additional conditions under which the test may be performed:

This can be important for the study of human liver diseases that are caused by an incorrect subcellular distribution of cell surface proteins, e.g., hepatocanalicular transport defects such as Dubin-Johnson Syndrome and progressive familial intrahepatic cholestasis (PFIC), and familial hypercholesterolemia.

Among these, 16 genes have been determined and 14 of these are related with diseases present in humans such as cystic fibrosis, adrenoleukodystrophy, Stargadt's disease, drug-resistant tumors, Dubin-Johnson syndrome, Byler's disease, progressive familiar intrahepatic cholestasis, X-linked sideroblastic anemia, ataxia, and persistent and hyperinsulimenic hypoglycemia in children.

Chronic Idiopathic Jaundice Conjugated Hyperbilirubinemia DJS Hyperbilirubinemia II None Dubin Johnson Syndrome is a rare genetic liver disorder that tends to affect people of Middle Eastern Jewish heritage disproportionately to other groups.