Liver disorder

disease
On 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

FieldValue
Canonical nameliver disorder
Mondo IDMONDO:0005154
EFOEFO:0001421
MeSHD008107
DOIDDOID:409
ICD-10-CMK70-K77
ICD-111784240230
NCITC3196
SNOMED CT235856003
UMLSC4021780
MedGen893061
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 disorderhepatobiliary disorderliver 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

rsIDp-valueGeneRisk alleleOdds ratio
rs7384091e-323PNPLA3C0.39
rs585429264e-119TM6SF2C0.31
rs37472074e-78PNPLA3G0.37
chr22:439288472e-77G0.25
rs67488104e-76ABCG8A1.67
rs20018463e-46TRIB1 - TRIB1ALT0.11
rs69825029e-45TRIB1ALC0.12
rs286017615e-44TRIB1ALC0.12
rs7800932e-38GCKRT0.1
chr2:277524638e-37G0.11
rs12603263e-36GCKRT0.1
rs7800942e-35GCKRT0.1
rs119778811e-33ABCB4 - ABCB1T1.73
rs289294747e-33SERPINA1C0.39
rs101071829e-33UBXN2B - CYP7A1C1.39
chr19:192595311e-30T0.24
rs2963915e-28LINC01595C0.63
rs4293582e-27APOET0.14
rs51172e-26APOC1T0.1
rs26424388e-26MTARC1A0.1
rs18009612e-22HNF4AC0.55
rs726231769e-22ABCB11G1.74
rs1126352992e-21SERPINA2 - SERPINA1G0.27
rs716333592e-20KLHL8 - MIR5705T0.09
rs285283088e-20KLHL8 - MIR5705G0.08
rs286797281e-19KLHL8 - MIR5705G0.08
rs100309374e-17TRMT10AA0.07
rs93967849e-17SUMO2P13 - FAM8A1G1.27
rs7384081e-16PNPLA3C0.15
rs284977202e-16MTTPC0.07

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90476081Verma A202430,744401,215Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90473867UK Biobank Whole-Genome Sequencing Consortium202520,073438,367Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90473876UK Biobank Whole-Genome Sequencing Consortium202515,256443,184Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90476080Verma A20248,971107,387Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90475246Verma A20248,715306,953Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90475270Verma A20248,449307,219Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90476079Verma A20246,33450,421Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90476082Verma A20246,13650,681Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90081521Backman JD20216,098381,358Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90085507Backman JD20216,098381,358Exome sequencing and analysis of 454,787 UK Biobank participants.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding9
Tier 2: splice/UTR0
Tier 3: regulatory0
Tier 4: intronic/intergenic41

MAF distribution

BucketVariants
common (>=0.05)40
low_freq (0.01-0.05)1
rare (<0.01)3
unknown6

Functional consequences

ConsequenceCount
intron_variant26
unknown9
missense_variant8
intergenic_variant3
non_coding_transcript_exon_variant2
stop_gained1
synonymous_variant1

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
rs7384092243928847C>A,G,T0.224missense_variantPNPLA31e-323Tier 1: coding
rs585429261919268740C>A,T0.065stop_gainedTM6SF24e-119Tier 1: coding
rs37472072243928975G>A,C,T0.404intron_variantPNPLA34e-78Tier 4: intronic/intergenic
chr22:439288472e-77Tier 4: intronic/intergenic
rs6748810243843796A>G,T0.05non_coding_transcript_exon_variantABCG84e-76Tier 4: intronic/intergenic
rs20018468125466208T>A,C,G0.429intergenic_variantTRIB1 - TRIB1AL3e-46Tier 4: intronic/intergenic
rs69825028125467120C>T0.49intron_variantTRIB1AL9e-45Tier 4: intronic/intergenic
rs286017618125487789C>G0.415intron_variantTRIB1AL5e-44Tier 4: intronic/intergenic
rs780093227519736T>A,C,G0.349intron_variantGCKR2e-38Tier 4: intronic/intergenic
chr2:277524630.4138e-37Tier 4: intronic/intergenic
rs1260326227508073T>A,C,G0.355missense_variantGCKR3e-36Tier 1: coding
rs780094227518370T>A,C,G0.403intron_variantGCKR2e-35Tier 4: intronic/intergenic
rs11977881787485697T>C,G0.05intergenic_variantABCB4 - ABCB11e-33Tier 4: intronic/intergenic
rs289294741494378610C>A,G,T0.05missense_variantSERPINA17e-33Tier 1: coding
rs10107182858480178C>A,T0.05intergenic_variantUBXN2B - CYP7A19e-33Tier 4: intronic/intergenic
chr19:192595311e-30Tier 4: intronic/intergenic
rs2963911947865277C>A,G,T0.05non_coding_transcript_exon_variantLINC015955e-28Tier 4: intronic/intergenic
rs4293581944908684T>C0.14missense_variantAPOE2e-27Tier 1: coding
rs51171944915533T>A,C,G0.223intron_variantAPOC12e-26Tier 4: intronic/intergenic
rs26424381220796686A>C,G,T0.296missense_variantMTARC18e-26Tier 1: coding
rs18009612044413724C>T0.05missense_variantHNF4A2e-22Tier 1: coding
rs726231762168977860G>A0.05intron_variantABCB119e-22Tier 4: intronic/intergenic
rs1126352991494371805G>A,C,T0.018intron_variantSERPINA2 - SERPINA12e-21Tier 4: intronic/intergenic
rs71633359487262668T>C0.299intron_variantKLHL8 - MIR57052e-20Tier 4: intronic/intergenic
rs28528308487280348G>T0.229intron_variantKLHL8 - MIR57058e-20Tier 4: intronic/intergenic
rs28679728487265289G>A0.23intron_variantKLHL8 - MIR57051e-19Tier 4: intronic/intergenic
rs10030937499552566A>G0.256intron_variantTRMT10A4e-17Tier 4: intronic/intergenic
rs9396784617596908G>A,T0.05intron_variantSUMO2P13 - FAM8A19e-17Tier 4: intronic/intergenic
rs7384082243928850C>A,G,T0.223synonymous_variantPNPLA31e-16Tier 4: intronic/intergenic
rs28497720499566213C>A,G,T0.256intron_variantMTTP2e-16Tier 4: intronic/intergenic

ClinVar germline variants

1 retrieved; paginated sample, class counts are floors:

1 conflicting classifications of pathogenicity

ClinVarVariant (HGVS)GeneClassificationReview
804425NM_003803.4(MYOM1):c.3260G>A (p.Trp1087Ter)MYOM1Conflicting classifications of pathogenicitycriteria 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.

GeneClassificationInheritanceDiseaseRecords
DECR1LimitedAutosomal recessiveliver disorder2

Cohort genes → proteins

3 cohort genes, 3 distinct canonical proteins.

Evidence partition

SubsetGenes
gwas_only1
multi_evidence2

Cohort genes (full)

SymbolHGNCEnsemblUniProtNameEvidence
DECR1HGNC:2753ENSG00000104325Q166982,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing], mitochondrialgencc
THBS2HGNC:11786ENSG00000186340P35442Thrombospondin-2gwas
MYOM1HGNC:7613ENSG00000101605P52179Myomesin-1clinvar

Cohort function summary

Lead sentence per gene, UniProt-curated.

SymbolProtein nameFunction (lead sentence)
DECR12,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing], mitochondrialAuxiliary enzyme of beta-oxidation.
THBS2Thrombospondin-2Adhesive glycoprotein that mediates cell-to-cell and cell-to-matrix interactions.
MYOM1Myomesin-1Major 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.

FamilyGenesFoldFDR
Antibody/Immunoglobulin19.7×0.298
Enzyme (other)14.0×0.345
Other/Unknown10.6×0.914

Per-gene assignment

SymbolFamilyDruggable?ECInterPro (top 3)
DECR1Enzyme (other)yes1.3.1.124SDR_fam, NAD(P)-bd_dom_sf
THBS2Other/UnknownnoEGF, TSP1_rpt, VWF_dom
MYOM1Antibody/ImmunoglobulinyesIg_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)

BucketGenes
narrow (1-5 tissues)0
moderate (6-20)0
broad (>20)3
unknown0

Top tissues across cohort

TissueCohort genes
heart right ventricle1
left ventricle myocardium1
right adrenal gland1
pericardium1
right coronary artery1
stromal cell of endometrium1
gluteal muscle1
hindlimb stylopod muscle1
skeletal muscle tissue of rectus abdominis1

Per-gene tissue summary (top 30)

SymbolBgee breadthFANTOM5 breadthSCXATop tissues
DECR1296ubiquitousmarkerleft ventricle myocardium, heart right ventricle, right adrenal gland
THBS2272ubiquitousmarkerpericardium, right coronary artery, stromal cell of endometrium
MYOM1215broadmarkerhindlimb 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)

SymbolInteractor count
DECR14,079
THBS23,405
MYOM11,082

Structural data

PDB: 3 · AlphaFold-only: 0 · No structure: 0

Cohort genes with PDB structures (top 30)

SymbolUniProtPDB entries
MYOM1P521799
DECR1Q166983
THBS2P354422

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.

PathwayCohort genesFoldFDRSample cohort genes
mitochondrial fatty acid beta-oxidation of unsaturated fatty acids1951.7×0.004DECR1
Defective B3GALTL causes PpS1154.3×0.008THBS2
O-glycosylation of TSR domain-containing proteins1150.3×0.008THBS2
Signaling by PDGF1126.9×0.008THBS2

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 termCohort genesFoldFDRSample cohort genes
extraocular skeletal muscle development1936.2×0.011MYOM1
obsolete protein kinase A signaling1468.1×0.011MYOM1
sarcomere organization1127.7×0.017MYOM1
fatty acid beta-oxidation1124.8×0.017DECR1
positive regulation of protein secretion1114.6×0.017MYOM1
positive regulation of synapse assembly181.4×0.020THBS2
negative regulation of angiogenesis156.2×0.023THBS2
positive regulation of cold-induced thermogenesis154.5×0.023DECR1
positive regulation of gene expression112.9×0.078MYOM1
cell adhesion112.5×0.078THBS2

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.

DrugDevelopment status
Cholic AcidApproved (phase 4)
Givosiran SodiumApproved (phase 4)
MetreleptinApproved (phase 4)
AdemetioninePhase 3 (in late-stage trials)
AvatrombopagPhase 3 (in late-stage trials)
Biphenyl Dimethyl DicarboxylatePhase 3 (in late-stage trials)
BupivacainePhase 3 (in late-stage trials)
DextrosePhase 3 (in late-stage trials)
FentanylPhase 3 (in late-stage trials)
Fibrinogen, HumanPhase 3 (in late-stage trials)
FilgrastimPhase 3 (in late-stage trials)
GabexatePhase 3 (in late-stage trials)
PioglitazonePhase 3 (in late-stage trials)
UrsodiolPhase 3 (in late-stage trials)
Vitamin EPhase 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

SymbolMoleculesMax phase
DECR100
THBS200
MYOM100

Bioactivity and enzyme data

Enzyme cohort genes (≥1 EC): 1.

Cohort genes with ChEMBL bioactivity (full, sorted by assay count)

SymbolAssaysType breakdown
DECR11Binding:1

Cohort enzymes (BRENDA EC)

SymbolEC numbersNames
DECR11.3.1.1242,4-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):

TierDefinitionGenesSymbols
AApproved (phase 4 drug)0
BPhased (≥1) drug, not yet approved0
CDruggable family + PDB, no drug2DECR1, MYOM1
DDruggable family + AlphaFold only, no drug0
EDifficult family or no structure, no drug1THBS2

Undrugged target profiles

3 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).

SymbolChEMBL assaysDrugged partners (top 3)
DECR11
THBS20
MYOM10

Clinical trials & evidence

Clinical trials

Clinical trials: 599.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified433
PHASE449
PHASE139
PHASE234
PHASE322
PHASE2/PHASE311
PHASE1/PHASE210
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04073290PHASE4RECRUITINGPrevention of Post-TIPS Hepatic Encephalopathy by Administration of Rifaximin and Lactulose
NCT04588077PHASE4RECRUITINGComparison Between 2-dose Versus 3-dose Regimens of Heplisav B in Cirrhosis
NCT06144112PHASE4NOT_YET_RECRUITINGFibrinogen Concentrates Versus Cryoprecipitate in Liver Transplant Surgery
NCT07150624PHASE4RECRUITINGThe Treatment of Liver Injury After Liver Resection With Polyene Phosphatidylcholine
NCT00148031PHASE4COMPLETEDImproving Hepatitis C Treatment in Injection Drug Users
NCT00152607PHASE4TERMINATEDOrthotopic Liver Transplantation Using a Living Donor
NCT00155376PHASE4UNKNOWNIntravenous-Morphine and Glucagon-Usage Enhanced MR Cholangiography
NCT00206076PHASE4COMPLETEDMycophenolate Mofetil Immunosuppression Without/With Reduced Dose Calcineurin Inhibitor Long After Liver Transplantation
NCT00222664PHASE4COMPLETEDQidong Hepatitis B Intervention Study
NCT00402402PHASE4COMPLETEDComparison of Quantiferon-TB Gold Assay With Tuberculin Skin Testing in Patients With Chronic Liver Disease
NCT00526331PHASE4COMPLETEDEvaluation of Arterial Pressure Based Cardiac Output for Goal-Directed Perioperative Therapy
NCT00564538PHASE4UNKNOWNA Study of Thymoglobulin and Tacrolimus in Liver Transplant
NCT00657124PHASE4COMPLETEDEffect of Preoperative Supplementation in Insulin Resistance
NCT00659698PHASE4COMPLETEDEffect of an Artificial Pancreas in Patients Undergoing Hepatic Resection
NCT00742326PHASE4TERMINATEDPioglitazone to Treat Fatty Liver in Patients With HIV and Hepatitis C Infections
NCT00799851PHASE4COMPLETEDA Randomized Controlled Trial Comparing Band Ligation and Cyanoacrylate Injection for Esophageal Varices
NCT00948220PHASE4COMPLETEDInfluence of Antiviral Therapy on Bone Mineral Density and Metabolism in Patients With Chronic Hepatitis C
NCT01148706PHASE4COMPLETEDEffectiveness of ActiSight™ Needle Guidance System in Patients Undergoing CT-Guided Procedures
NCT01195181PHASE4COMPLETEDDifferent PEG-interferon and Ribavirin Schedules for Chronic Hepatitis C in the Real Clinical Practice.
NCT01303549PHASE4COMPLETEDAnidulafungin vs Amphotericin B Safety in High Risk Hepatic Transplant Recipients
NCT01337440PHASE4UNKNOWNEfficacy and Safety of Ursodeoxycholic Acid (UDCA) Added to the DPP-4 Inhibitor in People With Type 2 Diabetes and Chronic Liver Diseases
NCT01429779PHASE4UNKNOWNThe Orange-III Trial: Optimised Recovery With Movicol® Preoperatively Within an Enhanced Recovery Programme
NCT01600105PHASE4COMPLETEDDetection of Liver Fibrosis With Magnetic Resonance Imaging (MRI)
NCT01650181PHASE4COMPLETEDEffects of Siliphos-Selenium-Methionine-Alpha Lipoic Acid in Patients With Fatty Liver and Non-alcoholic Steatohepatitis
NCT01958190PHASE4COMPLETEDStudy Comparing in Livertransplantation Recipients With Tacrolimus Alone Versus Tacrolimus&Sirolimus
NCT01968395PHASE4COMPLETEDPharmacokinetics of Caspofungin After One Dose in Patients With Liver Failure
NCT02347319PHASE4COMPLETEDTo Evaluate the Efficacy of DDB/Garlic Oil in Patients With Elevated Transaminase Chronic Liver Disease
NCT02366845PHASE4COMPLETEDProspective Validation of a Plasma Transfusion Dosing Algorithm in Patients With Chronic Liver Disease
NCT02489045PHASE4COMPLETEDNoninvasive Subharmonic Aided Pressure Estimation of Portal Hypertension
NCT02499185PHASE4TERMINATEDStudy Evaluating Novel Biomarkers of AKI (Acute Kidney Injury) in Post-operative Patients
NCT02712775PHASE4WITHDRAWNMinocycline Administration During Human Liver Transplantation
NCT02717949PHASE4TERMINATEDOral Hepatitis C Treatment for Indolent Lymphoma (OPTImaL) Study
NCT02764671PHASE4UNKNOWNSafety and Immunogenicity of Recombinant Hepatitis B Vaccines in the Neonates
NCT02938013PHASE4COMPLETEDdeLIVER: Direct Acting Antiviral Effects on the Liver
NCT02949492PHASE4TERMINATEDLow-dose IL-2 for Treg Expansion and Tolerance (LITE)
NCT03063866PHASE4UNKNOWNRandomised Controlled Study of Popofol Versus Midazolam as Sedation in Endoscopy With Advanced Liver Disease.
NCT03512210PHASE4COMPLETEDMonitoring SOF/VEL in Treatment Naïve, HCV Participants With Active Infection
NCT03522688PHASE4UNKNOWNImpact of Dexmedetomidine on Acute Kidney Injury Following Living Donor Liver Transplantation
NCT03646292PHASE4COMPLETEDAntidiabetic Drugs for Steatotic Liver Disease
NCT03652636PHASE4COMPLETEDEvaluation of the Efficacy of Contrast Enhanced Ultrasound Compared to MRI for Differentiation of Hepatic Lesions

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
RIBAVIRIN47
ENTECAVIR ANHYDROUS43
KETOTIFEN43
LACTULOSE43
SOFOSBUVIR43
ELTROMBOPAG42
LANREOTIDE42
PIOGLITAZONE42
TACROLIMUS ANHYDROUS42
VITAMIN E42
ALCOHOL41
ALEMTUZUMAB41
ANIDULAFUNGIN41
AVATROMBOPAG MALEATE41
CASPOFUNGIN41
COLESEVELAM41
DALTEPARIN SODIUM41
DEXTROSE41
EMPAGLIFLOZIN41
FIBRINOGEN I 12541
GLUCAGON41
HYDROMORPHONE HYDROCHLORIDE41
LEDIPASVIR41
LUSUTROMBOPAG41
METHYLENE BLUE41
METHYLENE BLUE ANHYDROUS41
METHYLENE BLUE CATION41
MORPHINE41
MYCOPHENOLATE MOFETIL41
OCTREOTIDE41