Dubin-Johnson syndrome
MeSH: D007566ORPHA: 234
Overview
rare, autosomal recessive, benign disorder that causes an isolated increase of conjugated bilirubin in the serum
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with Dubin-Johnson syndrome, sourced from HPO and Orphanet clinical annotations.
JaundiceBiliary tract abnormalityAbnormality of the liverAbnormality of coagulationFeverAbdominal painHepatomegalyConjugated hyperbilirubinemiaAbnormal gastric mucosa morphologyAbnormal urinary colorFatigue
Classification & Codes
MeSH Code
D007566Orphanet Code
ORPHA:234Dubin-Johnson syndrome
| MeSH | D007566 |
| Orphanet | ORPHA:234 |
| Treatments | 0 drug(s) |
| Symptoms on record | 11 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO