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Reference

Evidence

Compounds
Outcomes
Proteins
Interactions
Papers
Articles

Chemistry

Reactions
Reach

Reference layer

Pathways
Processes
Anatomy
Cell types
Organisms
Materials
Assessments
Diseases

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Computational infrastructure for human biology, built on a provenance-aware knowledge graph. Findings retain their sources; research and simulation are the next layers.

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A reference for what the literature reports. Not medical advice.

Disease

hereditary hyperbilirubinemia

MONDO:0002408Mondo

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Findings

No curated finding names hereditary hyperbilirubinemia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

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.

Definition from the Mondo Disease Ontology (MONDO:0002408), read 2026-09-29. CC BY 4.0.

Where it sits

A kind of: hyperbilirubinemia
inborn disorder of bilirubin metabolism
Narrower terms (7): Crigler-Najjar syndrome
Dubin-Johnson syndrome
Gilbert syndrome
hyperbilirubinemia, conjugated, type 3
hyperbilirubinemia, shunt, primary
Rotor syndrome
transient familial neonatal hyperbilirubinemia