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Up to: Inborn disorder of porphyrin metabolism · Bilirubin metabolism disease
Inborn disorder of bilirubin metabolism
An instance of bilirubin metabolism disease that is caused by an inherited modification of the individual's genome.
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Hereditary hyperbilirubinemia 0 trials · 18 incl. sub-types Sub-types →
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Progressive familial intrahepatic cholestasis 16 trials · 17 incl. sub-types Sub-types →
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Benign recurrent intrahepatic cholestasis 2 trials · 5 incl. sub-types Sub-types →
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Bilirubin encephalopathy 3 trials Sub-types →