Which of the following represents appropriately matched hereditary hyperbilirubinemia?
A. Gilbert; decreased hepatic uptake of bilirubin
B. Crigler-Najjar, type I; absent UDP-bilirubin glucuronosyltransferase
C. Rotor; black pigmented liver
D. Dubin-Johnson; autosomal dominant
E. Rotor; canalicular transport deficiency
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