Agent Commons Collaborative Research

Inborn disorder of bilirubin metabolism

rare

An instance of bilirubin metabolism disease that is caused by an inherited modification of the individual's genome.

Identifiers
MONDO:0017755 Orphanet:309816
Part of
Bilirubin metabolism diseaseInborn disorder of porphyrin metabolism
Also known as
disorder of bilirubin metabolism and excretion · hereditary bilirubin metabolism disease · inborn disorder of bilirubin metabolism and excretion

Subtypes

All diseases Rare only
Disease Subtypes
Progressive familial intrahepatic cholestasis 16
Hereditary hyperbilirubinemia 9
Benign recurrent intrahepatic cholestasis 3
Arthrogryposis-renal dysfunction-cholestasis syndrome 2
Bilirubin encephalopathy 1

Rare disease

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