Congenital biliary atresia

disorder

SNOMED 77480004CUI C0005411

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Research Evidence

Peer-reviewed studies linked via MeSH term "Biliary Atresia" from the MEDLINE/PubMed database.

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Artificial intelligence performance in image-based biliary atresia identification: a systematic review and meta-analysis.

[object Object], [object Object], [object Object] et al. · Eur J Radiol · 2026

PMID: 41499913Meta-Analysis

The diagnostic accuracy of MMP-7 for the diagnosis for biliary atresia- a systematic review and meta-analysis.

[object Object], [object Object], [object Object] · BMC Pediatr · 2025

PMID: 40855281Meta-AnalysisFull text (PMC)

Aspartate Aminotransferase-to-platelet Ratio Index (APRi) as Biomarker for Liver Damage in Biliary Atresia (BA): A Meta-analysis.

[object Object], [object Object], [object Object] et al. · J Pediatr Surg · 2025

PMID: 39923745Meta-Analysis

Risk factors for cholangitis after Kasai procedure in biliary atresia patients: a systematic review and meta-analysis.

[object Object], [object Object], [object Object] et al. · Int J Surg · 2025

PMID: 40844888Meta-AnalysisFull text (PMC)

The diagnostic performance of ultrasound features for biliary atresia: a systematic review and updated meta-analysis.

[object Object], [object Object], [object Object] et al. · Pediatr Surg Int · 2025

PMID: 40824323Meta-Analysis

Serum matrix metalloproteinase-7 (MMP-7) as a Biomarker for differentiating biliary atresia from neonatal hepatitis: evidence synthesis through systematic review and meta-analysis.

[object Object], [object Object], [object Object] et al. · Pediatr Surg Int · 2025

PMID: 40849391Meta-Analysis

Comparison for the diagnostic performance of early diagnostic methods for biliary atresia: a systematic review and network meta-analysis.

[object Object], [object Object], [object Object] et al. · Pediatr Surg Int · 2024

PMID: 38822892Meta-Analysis

Systematic review of the mechanism and assessment of liver fibrosis in biliary atresia.

[object Object], [object Object], [object Object] et al. · Pediatr Surg Int · 2024

PMID: 39033225Meta-Analysis

Comparison of different Kasai portoenterostomy techniques in the outcomes of biliary atresia: a systematic review and network meta-analysis.

[object Object], [object Object], [object Object] et al. · Pediatr Surg Int · 2024

PMID: 39592482Meta-Analysis

Population-based screening strategies for biliary atresia in the newborn: A systematic review and meta-analysis.

[object Object], [object Object], [object Object] et al. · PLoS One · 2024

PMID: 39197055Meta-AnalysisFull text (PMC)

Search all PubMed articles for Congenital biliary atresia

Research data from MEDLINE/PubMed

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Slowed or blocked flow of bile from liver

Very frequent (80-99%)HP:0001396

Undergrowth

Very frequent (80-99%)HP:0001508

Yellowing of the skin

Very frequent (80-99%)HP:0000952

Atretic gallbladder

Frequent (30-79%)HP:0011984

Conjugated hyperbilirubinemia

Frequent (30-79%)HP:0002908

Dark yellow urine

Frequent (30-79%)HP:0040321

Discolored, acholic stools

Frequent (30-79%)HP:0011985

Elevated alkaline phosphatase

Frequent (30-79%)HP:0003155

Elevated gamma-glutamyltransferase level

Frequent (30-79%)HP:0030948

Elevated serum transaminases

Frequent (30-79%)HP:0002910

Enlarged liver

Frequent (30-79%)HP:0002240

Fat malabsorption

Frequent (30-79%)HP:0002630

Liver dysfunction, mild

Frequent (30-79%)HP:0001410

Low factor II activity

Frequent (30-79%)HP:0008151

Prolonged neonatal jaundice

Frequent (30-79%)HP:0006579

Severe weight faltering

Frequent (30-79%)HP:0001525

Cirrhosis

Occasional (5-29%)HP:0001394

Distortion of face

Occasional (5-29%)HP:0001999

Eye muscle paralysis

Occasional (5-29%)HP:0000602

Hypopituitarism

Occasional (5-29%)HP:0040075

Hypothyroidism

Occasional (5-29%)HP:0000821

Large spleen

Occasional (5-29%)HP:0001744

Low birth weight

Occasional (5-29%)HP:0001518

Periportal fibrosis

Occasional (5-29%)HP:0001405

Proliferation of bile canaliculi

Occasional (5-29%)HP:0001408

Seizures

Occasional (5-29%)HP:0001250

Skin itching

Occasional (5-29%)HP:0000989

Xanthelasma of periocular region

Very rare (1-4%)HP:0001114

Related Conditions

Atresia of hepatic ducts(child)

Intrahepatic biliary atresia(child)

Congenital atresia of extrahepatic bile duct(child)

Ichthyosis congenita with biliary atresia(child)

Biliary atresia with splenic malformation syndrome(child)

Congenital anomaly of bile ducts(parent)

Quick Facts

SNOMED CT: 77480004
UMLS CUI: C0005411
Fully Specified Name: Congenital biliary atresia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 28

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.