Hepatobiliary disorder

disease
On this page

Also known as disease of hepatobiliary systemdisease or disorder of hepatobiliary systemdisorder of hepatobiliary systemhepatobiliary system diseasehepatobiliary system disease or disorderliver and biliary diseaseliver and biliary disorderliver and biliary system disorder

Summary

Hepatobiliary disorder (MONDO:0002515) is a disease and 5 clinical trials. Top therapeutic interventions include semaglutide and pentoxifylline. A subtype of digestive system disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 5

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namehepatobiliary disorder
Mondo IDMONDO:0002515
EFOEFO:0010284
DOIDDOID:3118
NCITC3959
UMLSC0267792
MedGen82758
Anatomy (UBERON)UBERON:0002423
Is cancer (heuristic)no

Also known as: disease of hepatobiliary system · disease or disorder of hepatobiliary system · disorder of hepatobiliary system · hepatobiliary disorder · hepatobiliary system disease · hepatobiliary system disease or disorder · liver and biliary disease · liver and biliary disorder · liver and biliary system disorder

Disease family

This is a subtype of digestive system disorder. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › digestive system disorderhepatobiliary disorder

Related subtypes (30): benign digestive system neoplasm, autoimmune disorder of gastrointestinal tract, gastrointestinal mucositis, diarrheal disease, pancreas disorder, digestive system cancer, peptic ulcer disease, stomach disorder, intestinal disorder, Meckel diverticulum, Cronkhite-Canada syndrome, diverticulosis, small-intestinal, diverticulosis of bowel, hernia, and retinal detachment, congenital enteropathy due to enteropeptidase deficiency, hereditary mixed polyposis syndrome, caudal duplication, Moyamoya disease with early-onset achalasia, hyperplastic polyposis syndrome, thoraco-abdominal enteric duplication, digestive duplication, juvenile polyposis syndrome, umbilical cord ulceration-intestinal atresia syndrome, growth retardation-mild developmental delay-chronic hepatitis syndrome, common mesentery, neoplasm of oropharynx, gastrointestinal polyp, digestive system neuroendocrine neoplasm, digestive system infectious disorder, upper digestive tract disorder, congenital peritoneal encapsulation

Subtypes (4): hepatobiliary neoplasm, biliary tract disorder, liver disorder, gallbladder disorder

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 5.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE22
Not specified2
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02970942PHASE2COMPLETEDInvestigation of Efficacy and Safety of Three Dose Levels of Subcutaneous Semaglutide Once Daily Versus Placebo in Subjects With Non-alcoholic Steatohepatitis.
NCT06944704PHASE2COMPLETEDEvaluation of Efficacy, Safety and Molecular Mechanism of Pentoxifylline Supplementation in Patients With Hepatic and Obstructive Jaundice
NCT03357380PHASE1COMPLETEDA Study on How Semaglutide Works on Early Stages of Scar Tissue in the Liver Assessed by Pictures of the Liver
NCT05481398Not specifiedCOMPLETEDA Randomized Controlled Trial Evaluating the Role of Negative Pressure Wound Therapy (NPWT) for Incisional Surgical Site Infections in Patients Undergoing Hepatopancreatobiliary Surgery
NCT06468787Not specifiedCOMPLETEDKosmos Anatomical Object Labeling and View Identification Pivotal Study

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
SEMAGLUTIDE42
PENTOXIFYLLINE41