biliary atresia
MeSH: D001656ORPHA: 30391
Overview
congenital disorder of digestive system investigation of choice of the disease is MRCP
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 biliary atresia, sourced from HPO and Orphanet clinical annotations.
JaundiceCholestasisFailure to thriveDecreased liver functionSevere failure to thriveHepatomegalyFat malabsorptionConjugated hyperbilirubinemiaElevated circulating hepatic transaminase concentrationElevated circulating alkaline phosphatase concentrationProlonged neonatal jaundiceProlonged prothrombin timeAtretic gallbladderAcholic stoolsElevated gamma-glutamyltransferase levelDark yellow urineOphthalmoplegiaHypothyroidismPruritusSeizureCirrhosisPeriportal fibrosisBile duct proliferationSmall for gestational ageSplenomegalyAbnormal facial shapeHypopituitarismXanthelasma
Classification & Codes
MeSH Code
D001656Orphanet Code
ORPHA:30391biliary atresia
| MeSH | D001656 |
| Orphanet | ORPHA:30391 |
| Treatments | 0 drug(s) |
| Symptoms on record | 28 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO