An instance of bilirubin metabolism disease that is caused by an inherited modification of the individual's genome.
Comprehensive, easy-to-understand information about this condition
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hereditary hyperbilirubinemia
MONDO:0002408
heme oxygenase 1 deficiency
MONDO:0013536
progressive familial intrahepatic cholestasis
MONDO:0015762
arthrogryposis-renal dysfunction-cholestasis syndrome
MONDO:0017123
bilirubin encephalopathy
MONDO:0018477
benign recurrent intrahepatic cholestasis
MONDO:0019008