Category
page 1Heme metabolism disorders
Gilbert syndrome
metabolic disorder in which the liver processes bilirubin slowly
Crigler-Najjar syndrome
bilirubin metabolic disorder that involves a build up of bilirubin as bilirubin is not being broken down as a result of a lack or deficiency of the enzyme uridine diphosphate glycosyltransferase (UGT)
Dubin-Johnson syndrome
rare, autosomal recessive, benign disorder that causes an isolated increase of conjugated bilirubin in the serum
Rotor syndrome
rare disease
Lucey–Driscoll syndrome
autosomal recessive metabolic disorder affecting enzymes involved in bilirubin metabolism
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