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inborn disorder of bilirubin metabolism - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

inborn disorder of bilirubin metabolism

MONDO:0017755

Also known as:disorder of bilirubin metabolismdisorder of bilirubin metabolism and excretionhereditary bilirubin metabolism disease

Overview

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

Diagnosis

Biomarker and diagnostic research for inborn disorder of bilirubin metabolism has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for inborn disorder of bilirubin metabolism.

46 publications have been identified in PubMed for inborn disorder of bilirubin metabolism. Research spans Case Report / Case Series (28%), Review / Meta-Analysis (24%), and Epidemiology / Natural History (24%).

Research Type	Count	% of Total
Patient case studies	13	28%

Data assembled from 3 of 12 sources · Last updated Sep 21, 2026, 4:52 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:309816

GARD

Genetic and Rare Diseases Info Center

GARD:21347

Questions for Your Care Team

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inborn disorder of bilirubin metabolism

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications