Liver disorder
diseaseOn this page
Also known as disease of liverdisease or disorder of liverdisorder of liverhepatic diseasehepatic disorderliver and intrahepatic bile duct disorderliver diseaseliver disease or disorder
Summary
Liver disorder (MONDO:0005154) is a disease (an umbrella term covering 32 Mondo subtypes) with 3 cohort genes (133 GWAS associations across 93 studies) and 599 clinical trials. Top therapeutic interventions include ribavirin, entecavir anhydrous, and ketotifen.
At a glance
- Umbrella term: 32 Mondo subtypes
- Cohort genes: 3
- GWAS associations: 133
- ClinVar variants: 1
- Clinical trials: 599
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | liver disorder |
| Mondo ID | MONDO:0005154 |
| EFO | EFO:0001421 |
| MeSH | D008107 |
| DOID | DOID:409 |
| ICD-10-CM | K70-K77 |
| ICD-11 | 1784240230 |
| NCIT | C3196 |
| SNOMED CT | 235856003 |
| UMLS | C4021780 |
| MedGen | 893061 |
| Anatomy (UBERON) | UBERON:0002107 |
| Is cancer (heuristic) | no |
Also known as: disease of liver · disease or disorder of liver · disorder of liver · hepatic disease · hepatic disorder · liver and intrahepatic bile duct disorder · liver disease · liver disease or disorder · liver disorder
Data availability: 1 ClinVar variant · 133 GWAS associations (93 studies) · 1 GenCC gene-disease record.
Disease family
An umbrella term covering 32 Mondo subtypes.
Classification path: disease › human disease › disease by body system or component › digestive system disorder › hepatobiliary disorder › liver disorder
Related subtypes (3): hepatobiliary neoplasm, biliary tract disorder, gallbladder disorder
Subtypes (32): polycystic echinococcosis, autosomal dominant polycystic liver disease, hepatorenal syndrome, hepatitis, hepatic vascular disorder, hepatic porphyria, hepatopulmonary syndrome, fatty liver disease, cirrhosis of liver, drug-induced liver injury, perinatal jaundice due to hepatocellular damage, Aagenaes syndrome, transient familial neonatal hyperbilirubinemia, hyperbiliverdinemia, transient infantile hypertriglyceridemia and hepatosteatosis, idiopathic copper-associated cirrhosis, familial intrahepatic cholestasis, bile duct cyst, nodular regenerative hyperplasia of the liver, hepatoportal sclerosis, primitive portal vein thrombosis, glycogen storage disease due to liver phosphorylase kinase deficiency, liver and intrahepatic bile duct neoplasm, alcoholic liver disease, early-onset familial noncirrhotic portal hypertension, liver failure, fibrotic liver disease, intestinal failure–associated liver disease, liver abscess (disease), membranous obstruction of inferior vena cava, liver disease, severe congenital, cystic fibrosis-related liver disease
Genetics & variants
GWAS landscape
133 GWAS associations across 93 studies. Top hits map to 28 distinct genes (as reported by GWAS).
Top associations by p-value
| rsID | p-value | Gene | Risk allele | Odds ratio |
|---|---|---|---|---|
| rs738409 | 1e-323 | PNPLA3 | C | 0.39 |
| rs58542926 | 4e-119 | TM6SF2 | C | 0.31 |
| rs3747207 | 4e-78 | PNPLA3 | G | 0.37 |
| chr22:43928847 | 2e-77 | G | 0.25 | |
| rs6748810 | 4e-76 | ABCG8 | A | 1.67 |
| rs2001846 | 3e-46 | TRIB1 - TRIB1AL | T | 0.11 |
| rs6982502 | 9e-45 | TRIB1AL | C | 0.12 |
| rs28601761 | 5e-44 | TRIB1AL | C | 0.12 |
| rs780093 | 2e-38 | GCKR | T | 0.1 |
| chr2:27752463 | 8e-37 | G | 0.11 | |
| rs1260326 | 3e-36 | GCKR | T | 0.1 |
| rs780094 | 2e-35 | GCKR | T | 0.1 |
| rs11977881 | 1e-33 | ABCB4 - ABCB1 | T | 1.73 |
| rs28929474 | 7e-33 | SERPINA1 | C | 0.39 |
| rs10107182 | 9e-33 | UBXN2B - CYP7A1 | C | 1.39 |
| chr19:19259531 | 1e-30 | T | 0.24 | |
| rs296391 | 5e-28 | LINC01595 | C | 0.63 |
| rs429358 | 2e-27 | APOE | T | 0.14 |
| rs5117 | 2e-26 | APOC1 | T | 0.1 |
| rs2642438 | 8e-26 | MTARC1 | A | 0.1 |
| rs1800961 | 2e-22 | HNF4A | C | 0.55 |
| rs72623176 | 9e-22 | ABCB11 | G | 1.74 |
| rs112635299 | 2e-21 | SERPINA2 - SERPINA1 | G | 0.27 |
| rs71633359 | 2e-20 | KLHL8 - MIR5705 | T | 0.09 |
| rs28528308 | 8e-20 | KLHL8 - MIR5705 | G | 0.08 |
| rs28679728 | 1e-19 | KLHL8 - MIR5705 | G | 0.08 |
| rs10030937 | 4e-17 | TRMT10A | A | 0.07 |
| rs9396784 | 9e-17 | SUMO2P13 - FAM8A1 | G | 1.27 |
| rs738408 | 1e-16 | PNPLA3 | C | 0.15 |
| rs28497720 | 2e-16 | MTTP | C | 0.07 |
Top studies (by case count)
| Study | Lead author | Year | Cases | Controls | Title |
|---|---|---|---|---|---|
| GCST90476081 | Verma A | 2024 | 30,744 | 401,215 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90473867 | UK Biobank Whole-Genome Sequencing Consortium | 2025 | 20,073 | 438,367 | Whole-genome sequencing of 490,640 UK Biobank participants. |
| GCST90473876 | UK Biobank Whole-Genome Sequencing Consortium | 2025 | 15,256 | 443,184 | Whole-genome sequencing of 490,640 UK Biobank participants. |
| GCST90476080 | Verma A | 2024 | 8,971 | 107,387 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90475246 | Verma A | 2024 | 8,715 | 306,953 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90475270 | Verma A | 2024 | 8,449 | 307,219 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90476079 | Verma A | 2024 | 6,334 | 50,421 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90476082 | Verma A | 2024 | 6,136 | 50,681 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90081521 | Backman JD | 2021 | 6,098 | 381,358 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
| GCST90085507 | Backman JD | 2021 | 6,098 | 381,358 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
Variant details and genetic-evidence tiers
Tier distribution (top 50 variants)
| Tier | Variants |
|---|---|
| Tier 1: coding | 9 |
| Tier 2: splice/UTR | 0 |
| Tier 3: regulatory | 0 |
| Tier 4: intronic/intergenic | 41 |
MAF distribution
| Bucket | Variants |
|---|---|
| common (>=0.05) | 40 |
| low_freq (0.01-0.05) | 1 |
| rare (<0.01) | 3 |
| unknown | 6 |
Functional consequences
| Consequence | Count |
|---|---|
| intron_variant | 26 |
| unknown | 9 |
| missense_variant | 8 |
| intergenic_variant | 3 |
| non_coding_transcript_exon_variant | 2 |
| stop_gained | 1 |
| synonymous_variant | 1 |
Top variants
| rsID | Chr | Pos | Alleles | MAF | Consequence | Gene | p-value | Tier |
|---|---|---|---|---|---|---|---|---|
| rs738409 | 22 | 43928847 | C>A,G,T | 0.224 | missense_variant | PNPLA3 | 1e-323 | Tier 1: coding |
| rs58542926 | 19 | 19268740 | C>A,T | 0.065 | stop_gained | TM6SF2 | 4e-119 | Tier 1: coding |
| rs3747207 | 22 | 43928975 | G>A,C,T | 0.404 | intron_variant | PNPLA3 | 4e-78 | Tier 4: intronic/intergenic |
| chr22:43928847 | 2e-77 | Tier 4: intronic/intergenic | ||||||
| rs6748810 | 2 | 43843796 | A>G,T | 0.05 | non_coding_transcript_exon_variant | ABCG8 | 4e-76 | Tier 4: intronic/intergenic |
| rs2001846 | 8 | 125466208 | T>A,C,G | 0.429 | intergenic_variant | TRIB1 - TRIB1AL | 3e-46 | Tier 4: intronic/intergenic |
| rs6982502 | 8 | 125467120 | C>T | 0.49 | intron_variant | TRIB1AL | 9e-45 | Tier 4: intronic/intergenic |
| rs28601761 | 8 | 125487789 | C>G | 0.415 | intron_variant | TRIB1AL | 5e-44 | Tier 4: intronic/intergenic |
| rs780093 | 2 | 27519736 | T>A,C,G | 0.349 | intron_variant | GCKR | 2e-38 | Tier 4: intronic/intergenic |
| chr2:27752463 | 0.413 | 8e-37 | Tier 4: intronic/intergenic | |||||
| rs1260326 | 2 | 27508073 | T>A,C,G | 0.355 | missense_variant | GCKR | 3e-36 | Tier 1: coding |
| rs780094 | 2 | 27518370 | T>A,C,G | 0.403 | intron_variant | GCKR | 2e-35 | Tier 4: intronic/intergenic |
| rs11977881 | 7 | 87485697 | T>C,G | 0.05 | intergenic_variant | ABCB4 - ABCB1 | 1e-33 | Tier 4: intronic/intergenic |
| rs28929474 | 14 | 94378610 | C>A,G,T | 0.05 | missense_variant | SERPINA1 | 7e-33 | Tier 1: coding |
| rs10107182 | 8 | 58480178 | C>A,T | 0.05 | intergenic_variant | UBXN2B - CYP7A1 | 9e-33 | Tier 4: intronic/intergenic |
| chr19:19259531 | 1e-30 | Tier 4: intronic/intergenic | ||||||
| rs296391 | 19 | 47865277 | C>A,G,T | 0.05 | non_coding_transcript_exon_variant | LINC01595 | 5e-28 | Tier 4: intronic/intergenic |
| rs429358 | 19 | 44908684 | T>C | 0.14 | missense_variant | APOE | 2e-27 | Tier 1: coding |
| rs5117 | 19 | 44915533 | T>A,C,G | 0.223 | intron_variant | APOC1 | 2e-26 | Tier 4: intronic/intergenic |
| rs2642438 | 1 | 220796686 | A>C,G,T | 0.296 | missense_variant | MTARC1 | 8e-26 | Tier 1: coding |
| rs1800961 | 20 | 44413724 | C>T | 0.05 | missense_variant | HNF4A | 2e-22 | Tier 1: coding |
| rs72623176 | 2 | 168977860 | G>A | 0.05 | intron_variant | ABCB11 | 9e-22 | Tier 4: intronic/intergenic |
| rs112635299 | 14 | 94371805 | G>A,C,T | 0.018 | intron_variant | SERPINA2 - SERPINA1 | 2e-21 | Tier 4: intronic/intergenic |
| rs71633359 | 4 | 87262668 | T>C | 0.299 | intron_variant | KLHL8 - MIR5705 | 2e-20 | Tier 4: intronic/intergenic |
| rs28528308 | 4 | 87280348 | G>T | 0.229 | intron_variant | KLHL8 - MIR5705 | 8e-20 | Tier 4: intronic/intergenic |
| rs28679728 | 4 | 87265289 | G>A | 0.23 | intron_variant | KLHL8 - MIR5705 | 1e-19 | Tier 4: intronic/intergenic |
| rs10030937 | 4 | 99552566 | A>G | 0.256 | intron_variant | TRMT10A | 4e-17 | Tier 4: intronic/intergenic |
| rs9396784 | 6 | 17596908 | G>A,T | 0.05 | intron_variant | SUMO2P13 - FAM8A1 | 9e-17 | Tier 4: intronic/intergenic |
| rs738408 | 22 | 43928850 | C>A,G,T | 0.223 | synonymous_variant | PNPLA3 | 1e-16 | Tier 4: intronic/intergenic |
| rs28497720 | 4 | 99566213 | C>A,G,T | 0.256 | intron_variant | MTTP | 2e-16 | Tier 4: intronic/intergenic |
ClinVar germline variants
1 retrieved; paginated sample, class counts are floors:
1 conflicting classifications of pathogenicity
| ClinVar | Variant (HGVS) | Gene | Classification | Review |
|---|---|---|---|---|
| 804425 | NM_003803.4(MYOM1):c.3260G>A (p.Trp1087Ter) | MYOM1 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications |
Genes & proteins
Mendelian disease overlap and somatic drivers
GenCC: 2 · Orphanet: 0 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0
GenCC gene–disease validity (cohort genes)
the Disease column is the GenCC-asserted condition — a cohort gene’s strongest validity may be for a related predisposition syndrome.
| Gene | Classification | Inheritance | Disease | Records |
|---|---|---|---|---|
| DECR1 | Limited | Autosomal recessive | liver disorder | 2 |
Cohort genes → proteins
3 cohort genes, 3 distinct canonical proteins.
Evidence partition
| Subset | Genes |
|---|---|
| gwas_only | 1 |
| multi_evidence | 2 |
Cohort genes (full)
| Symbol | HGNC | Ensembl | UniProt | Name | Evidence |
|---|---|---|---|---|---|
| DECR1 | HGNC:2753 | ENSG00000104325 | Q16698 | 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing], mitochondrial | gencc |
| THBS2 | HGNC:11786 | ENSG00000186340 | P35442 | Thrombospondin-2 | gwas |
| MYOM1 | HGNC:7613 | ENSG00000101605 | P52179 | Myomesin-1 | clinvar |
Cohort function summary
Lead sentence per gene, UniProt-curated.
| Symbol | Protein name | Function (lead sentence) |
|---|---|---|
| DECR1 | 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing], mitochondrial | Auxiliary enzyme of beta-oxidation. |
| THBS2 | Thrombospondin-2 | Adhesive glycoprotein that mediates cell-to-cell and cell-to-matrix interactions. |
| MYOM1 | Myomesin-1 | Major component of the vertebrate myofibrillar M band. |
Protein-family classification
Druggable: 2 · Difficult: 0 · Unknown: 1 · Druggable fraction: 0.67
Family distribution
Cohort families vs a genome-wide background (hypergeometric, BH-FDR; fold = observed/expected). Counts kept; sorted by enrichment, so the catch-all Other/Unknown bucket no longer leads.
| Family | Genes | Fold | FDR |
|---|---|---|---|
| Antibody/Immunoglobulin | 1 | 9.7× | 0.298 |
| Enzyme (other) | 1 | 4.0× | 0.345 |
| Other/Unknown | 1 | 0.6× | 0.914 |
Per-gene assignment
| Symbol | Family | Druggable? | EC | InterPro (top 3) |
|---|---|---|---|---|
| DECR1 | Enzyme (other) | yes | 1.3.1.124 | SDR_fam, NAD(P)-bd_dom_sf |
| THBS2 | Other/Unknown | no | EGF, TSP1_rpt, VWF_dom | |
| MYOM1 | Antibody/Immunoglobulin | yes | Ig_sub2, Ig_sub, FN3_dom |
Expression context
Cohort genes with no expression data: 0.
3 cohort genes are a single-cell marker in ≥1 SCXA experiment.
Breadth distribution (Bgee present_calls)
| Bucket | Genes |
|---|---|
| narrow (1-5 tissues) | 0 |
| moderate (6-20) | 0 |
| broad (>20) | 3 |
| unknown | 0 |
Top tissues across cohort
| Tissue | Cohort genes |
|---|---|
| heart right ventricle | 1 |
| left ventricle myocardium | 1 |
| right adrenal gland | 1 |
| pericardium | 1 |
| right coronary artery | 1 |
| stromal cell of endometrium | 1 |
| gluteal muscle | 1 |
| hindlimb stylopod muscle | 1 |
| skeletal muscle tissue of rectus abdominis | 1 |
Per-gene tissue summary (top 30)
| Symbol | Bgee breadth | FANTOM5 breadth | SCXA | Top tissues |
|---|---|---|---|---|
| DECR1 | 296 | ubiquitous | marker | left ventricle myocardium, heart right ventricle, right adrenal gland |
| THBS2 | 272 | ubiquitous | marker | pericardium, right coronary artery, stromal cell of endometrium |
| MYOM1 | 215 | broad | marker | hindlimb stylopod muscle, skeletal muscle tissue of rectus abdominis, gluteal muscle |
Protein interactions among cohort
Intra-cohort edges: 0.
Hub genes (top 10 by interactor count)
| Symbol | Interactor count |
|---|---|
| DECR1 | 4,079 |
| THBS2 | 3,405 |
| MYOM1 | 1,082 |
Structural data
PDB: 3 · AlphaFold-only: 0 · No structure: 0
Cohort genes with PDB structures (top 30)
| Symbol | UniProt | PDB entries |
|---|---|---|
| MYOM1 | P52179 | 9 |
| DECR1 | Q16698 | 3 |
| THBS2 | P35442 | 2 |
Function
Pathway analysis
Distinct Reactome pathways touched by cohort: 4. Enrichment computed across 3 evidence-associated genes (2 with Reactome annotation).
Pathways by enrichment
Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 2 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| Pathway | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| mitochondrial fatty acid beta-oxidation of unsaturated fatty acids | 1 | 951.7× | 0.004 | DECR1 |
| Defective B3GALTL causes PpS | 1 | 154.3× | 0.008 | THBS2 |
| O-glycosylation of TSR domain-containing proteins | 1 | 150.3× | 0.008 | THBS2 |
| Signaling by PDGF | 1 | 126.9× | 0.008 | THBS2 |
GO biological processes by enrichment
Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 3 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| GO term | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| extraocular skeletal muscle development | 1 | 936.2× | 0.011 | MYOM1 |
| obsolete protein kinase A signaling | 1 | 468.1× | 0.011 | MYOM1 |
| sarcomere organization | 1 | 127.7× | 0.017 | MYOM1 |
| fatty acid beta-oxidation | 1 | 124.8× | 0.017 | DECR1 |
| positive regulation of protein secretion | 1 | 114.6× | 0.017 | MYOM1 |
| positive regulation of synapse assembly | 1 | 81.4× | 0.020 | THBS2 |
| negative regulation of angiogenesis | 1 | 56.2× | 0.023 | THBS2 |
| positive regulation of cold-induced thermogenesis | 1 | 54.5× | 0.023 | DECR1 |
| positive regulation of gene expression | 1 | 12.9× | 0.078 | MYOM1 |
| cell adhesion | 1 | 12.5× | 0.078 | THBS2 |
Therapeutics
Drugs indicated for this disease
3 approved, 12 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.
| Drug | Development status |
|---|---|
| Cholic Acid | Approved (phase 4) |
| Givosiran Sodium | Approved (phase 4) |
| Metreleptin | Approved (phase 4) |
| Ademetionine | Phase 3 (in late-stage trials) |
| Avatrombopag | Phase 3 (in late-stage trials) |
| Biphenyl Dimethyl Dicarboxylate | Phase 3 (in late-stage trials) |
| Bupivacaine | Phase 3 (in late-stage trials) |
| Dextrose | Phase 3 (in late-stage trials) |
| Fentanyl | Phase 3 (in late-stage trials) |
| Fibrinogen, Human | Phase 3 (in late-stage trials) |
| Filgrastim | Phase 3 (in late-stage trials) |
| Gabexate | Phase 3 (in late-stage trials) |
| Pioglitazone | Phase 3 (in late-stage trials) |
| Ursodiol | Phase 3 (in late-stage trials) |
| Vitamin E | Phase 3 (in late-stage trials) |
Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Alemtuzumab, Alisporivir, Amlodipine, Cagrilintide, Cyclosporine, Eltrombopag, Fish Oil, Fish Oil Triglycerides, Icosapent, Maralixibat, Mycophenolate Mofetil, Pentoxifylline, Rafutrombopag, Semaglutide, Sirolimus, Sodium Chloride, Tacrolimus Anhydrous.
Drug target analysis
Approved (phase 4): 0 · Phase ≥3: 0 · Phased (≥1): 0 · Undrugged: 3
Druggability breadth: 1 of 3 evidence-associated genes (33%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).
Top cohort targets by molecule count
| Symbol | Molecules | Max phase |
|---|---|---|
| DECR1 | 0 | 0 |
| THBS2 | 0 | 0 |
| MYOM1 | 0 | 0 |
Bioactivity and enzyme data
Enzyme cohort genes (≥1 EC): 1.
Cohort genes with ChEMBL bioactivity (full, sorted by assay count)
| Symbol | Assays | Type breakdown |
|---|---|---|
| DECR1 | 1 | Binding:1 |
Cohort enzymes (BRENDA EC)
| Symbol | EC numbers | Names |
|---|---|---|
| DECR1 | 1.3.1.124 | 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing] |
Pharmacogenomics
Cohort genes with a PharmGKB record: 3; with CPIC/DPWG dosing guidelines: 0.
No cohort gene has a CPIC/DPWG genotype-guided dosing guideline (PharmGKB).
Chemical tractability of cohort targets
0 approved/phased compounds have measured bioactivity against a cohort gene (and aren’t yet in disease-level trials). This is a research / tractability signal, NOT a therapeutic recommendation — a bioactivity row often reflects off-target or screening binding (e.g. promiscuous kinase inhibitors against a cohort kinase), implying no disease mechanism.
Druggability pyramid
Cohort genes binned by druggability tier (high → low):
| Tier | Definition | Genes | Symbols |
|---|---|---|---|
| A | Approved (phase 4 drug) | 0 | |
| B | Phased (≥1) drug, not yet approved | 0 | |
| C | Druggable family + PDB, no drug | 2 | DECR1, MYOM1 |
| D | Druggable family + AlphaFold only, no drug | 0 | |
| E | Difficult family or no structure, no drug | 1 | THBS2 |
Undrugged target profiles
3 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).
| Symbol | ChEMBL assays | Drugged partners (top 3) |
|---|---|---|
| DECR1 | 1 | — |
| THBS2 | 0 | — |
| MYOM1 | 0 | — |
Clinical trials & evidence
Clinical trials
Clinical trials: 599.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 433 |
| PHASE4 | 49 |
| PHASE1 | 39 |
| PHASE2 | 34 |
| PHASE3 | 22 |
| PHASE2/PHASE3 | 11 |
| PHASE1/PHASE2 | 10 |
| EARLY_PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04073290 | PHASE4 | RECRUITING | Prevention of Post-TIPS Hepatic Encephalopathy by Administration of Rifaximin and Lactulose |
| NCT04588077 | PHASE4 | RECRUITING | Comparison Between 2-dose Versus 3-dose Regimens of Heplisav B in Cirrhosis |
| NCT06144112 | PHASE4 | NOT_YET_RECRUITING | Fibrinogen Concentrates Versus Cryoprecipitate in Liver Transplant Surgery |
| NCT07150624 | PHASE4 | RECRUITING | The Treatment of Liver Injury After Liver Resection With Polyene Phosphatidylcholine |
| NCT00148031 | PHASE4 | COMPLETED | Improving Hepatitis C Treatment in Injection Drug Users |
| NCT00152607 | PHASE4 | TERMINATED | Orthotopic Liver Transplantation Using a Living Donor |
| NCT00155376 | PHASE4 | UNKNOWN | Intravenous-Morphine and Glucagon-Usage Enhanced MR Cholangiography |
| NCT00206076 | PHASE4 | COMPLETED | Mycophenolate Mofetil Immunosuppression Without/With Reduced Dose Calcineurin Inhibitor Long After Liver Transplantation |
| NCT00222664 | PHASE4 | COMPLETED | Qidong Hepatitis B Intervention Study |
| NCT00402402 | PHASE4 | COMPLETED | Comparison of Quantiferon-TB Gold Assay With Tuberculin Skin Testing in Patients With Chronic Liver Disease |
| NCT00526331 | PHASE4 | COMPLETED | Evaluation of Arterial Pressure Based Cardiac Output for Goal-Directed Perioperative Therapy |
| NCT00564538 | PHASE4 | UNKNOWN | A Study of Thymoglobulin and Tacrolimus in Liver Transplant |
| NCT00657124 | PHASE4 | COMPLETED | Effect of Preoperative Supplementation in Insulin Resistance |
| NCT00659698 | PHASE4 | COMPLETED | Effect of an Artificial Pancreas in Patients Undergoing Hepatic Resection |
| NCT00742326 | PHASE4 | TERMINATED | Pioglitazone to Treat Fatty Liver in Patients With HIV and Hepatitis C Infections |
| NCT00799851 | PHASE4 | COMPLETED | A Randomized Controlled Trial Comparing Band Ligation and Cyanoacrylate Injection for Esophageal Varices |
| NCT00948220 | PHASE4 | COMPLETED | Influence of Antiviral Therapy on Bone Mineral Density and Metabolism in Patients With Chronic Hepatitis C |
| NCT01148706 | PHASE4 | COMPLETED | Effectiveness of ActiSight™ Needle Guidance System in Patients Undergoing CT-Guided Procedures |
| NCT01195181 | PHASE4 | COMPLETED | Different PEG-interferon and Ribavirin Schedules for Chronic Hepatitis C in the Real Clinical Practice. |
| NCT01303549 | PHASE4 | COMPLETED | Anidulafungin vs Amphotericin B Safety in High Risk Hepatic Transplant Recipients |
| NCT01337440 | PHASE4 | UNKNOWN | Efficacy and Safety of Ursodeoxycholic Acid (UDCA) Added to the DPP-4 Inhibitor in People With Type 2 Diabetes and Chronic Liver Diseases |
| NCT01429779 | PHASE4 | UNKNOWN | The Orange-III Trial: Optimised Recovery With Movicol® Preoperatively Within an Enhanced Recovery Programme |
| NCT01600105 | PHASE4 | COMPLETED | Detection of Liver Fibrosis With Magnetic Resonance Imaging (MRI) |
| NCT01650181 | PHASE4 | COMPLETED | Effects of Siliphos-Selenium-Methionine-Alpha Lipoic Acid in Patients With Fatty Liver and Non-alcoholic Steatohepatitis |
| NCT01958190 | PHASE4 | COMPLETED | Study Comparing in Livertransplantation Recipients With Tacrolimus Alone Versus Tacrolimus&Sirolimus |
| NCT01968395 | PHASE4 | COMPLETED | Pharmacokinetics of Caspofungin After One Dose in Patients With Liver Failure |
| NCT02347319 | PHASE4 | COMPLETED | To Evaluate the Efficacy of DDB/Garlic Oil in Patients With Elevated Transaminase Chronic Liver Disease |
| NCT02366845 | PHASE4 | COMPLETED | Prospective Validation of a Plasma Transfusion Dosing Algorithm in Patients With Chronic Liver Disease |
| NCT02489045 | PHASE4 | COMPLETED | Noninvasive Subharmonic Aided Pressure Estimation of Portal Hypertension |
| NCT02499185 | PHASE4 | TERMINATED | Study Evaluating Novel Biomarkers of AKI (Acute Kidney Injury) in Post-operative Patients |
| NCT02712775 | PHASE4 | WITHDRAWN | Minocycline Administration During Human Liver Transplantation |
| NCT02717949 | PHASE4 | TERMINATED | Oral Hepatitis C Treatment for Indolent Lymphoma (OPTImaL) Study |
| NCT02764671 | PHASE4 | UNKNOWN | Safety and Immunogenicity of Recombinant Hepatitis B Vaccines in the Neonates |
| NCT02938013 | PHASE4 | COMPLETED | deLIVER: Direct Acting Antiviral Effects on the Liver |
| NCT02949492 | PHASE4 | TERMINATED | Low-dose IL-2 for Treg Expansion and Tolerance (LITE) |
| NCT03063866 | PHASE4 | UNKNOWN | Randomised Controlled Study of Popofol Versus Midazolam as Sedation in Endoscopy With Advanced Liver Disease. |
| NCT03512210 | PHASE4 | COMPLETED | Monitoring SOF/VEL in Treatment Naïve, HCV Participants With Active Infection |
| NCT03522688 | PHASE4 | UNKNOWN | Impact of Dexmedetomidine on Acute Kidney Injury Following Living Donor Liver Transplantation |
| NCT03646292 | PHASE4 | COMPLETED | Antidiabetic Drugs for Steatotic Liver Disease |
| NCT03652636 | PHASE4 | COMPLETED | Evaluation of the Efficacy of Contrast Enhanced Ultrasound Compared to MRI for Differentiation of Hepatic Lesions |
Drugs tested across these trials (top 30)
Related Atlas pages
- Cohort genes: DECR1, THBS2, MYOM1
- Drugs: Ribavirin, Entecavir, Ketotifen, Lactulose, Sofosbuvir, Eltrombopag, Lanreotide, Pioglitazone, Tacrolimus, Vitamin E, Alcohol, Alemtuzumab, Anidulafungin, Avatrombopag, Caspofungin, Colesevelam, Dalteparin, Dextrose, Empagliflozin, FIBRINOGEN I 125, Glucagon, Hydromorphone, Ledipasvir, Lusutrombopag, Methylene Blue, Morphine, Mycophenolate Mofetil, Octreotide