Hereditary hyperbilirubinemia

MONDO:0002408

An inherited disorder affecting the metabolism of bilirubin. It results in increased levels of bilirubin in the blood. Representative examples of this condition include Gilbert syndrome and Crigler-Najjar syndrome.

Also known as: bilirubin metabolic disorder, hyperbilirubinaemia, hyperbilirubinemia, hereditary hyperbilirubinemia

18 clinical trials for this condition and its sub-types, 0 tagged with Hereditary hyperbilirubinemia itself.

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Where it sits in the disease tree

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Part of

↑ Inborn disorder of bilirubin metabolism (39) ↑ Hyperbilirubinemia (28)

Sub-types of Hereditary hyperbilirubinemia

Transient familial neonatal hyperbilirubinemia 18 trials
Crigler-Najjar syndrome 0 trials
2 sub-types
- Crigler-Najjar syndrome type 1 0 trials
- Crigler-Najjar syndrome type 2 0 trials
Dubin-Johnson syndrome 0 trials
Gilbert syndrome 0 trials
Rotor syndrome 0 trials
Hyperbilirubinemia, conjugated, type 3 0 trials
Hyperbilirubinemia, shunt, primary 0 trials

Including sub-types (18) Tagged with Hereditary hyperbilirubinemia (0)

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