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Disease · MONDO_0007648

hereditary diffuse gastric adenocarcinoma

6 sourcesdiseases-2026-09-18-0.1.0

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ConductScience Library. hereditary diffuse gastric adenocarcinoma. Diseases, record MONDO_0007648. Release diseases-2026-09-18-0.1.0, 18 Sept 2026. https://conductscience.org/library/diseases/MONDO_0007648

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Disease

Names and IDs as Open Targets gives them. Its IDs in MeSH, Orphanet, the Disease Ontology and the NCI Thesaurus are those Open Targets states for it.

Name
hereditary diffuse gastric adenocarcinoma
Open Targets
Open Targets ID
MONDO_0007648
Open Targets
Other names
FDGC, HDGC, familial diffuse cancer of stomach, familial diffuse gastric cancer, hereditary diffuse cancer of stomach, hereditary diffuse gastric cancer
Open Targets
Disease Ontology
DOID:0080764
Disease Ontology
NCI Thesaurus
C43295
NCI Thesaurus
Orphanet
ORPHA:26106
Orphanet
Highest stage of its drugs
Phase 3, for 3 of its 6 drugs, from ClinicalTrials.gov
Open Targets

Drugs6

The drugs Open Targets' clinical reports study for the disease, the highest stage first, then the most trial reports. The stage is Open Targets', the highest any of its sources reports for the pair, and each row names the sources that report it.

DrugChEMBL IDTypeOpen Targets' stageStage reported byReportsOf them trialsTrials shown hereSource
CAPECITABINECHEMBL1773Small moleculePhase 3ClinicalTrials.gov111Drugs and targets
OXALIPLATINCHEMBL414804Small moleculePhase 3ClinicalTrials.gov111Drugs and targets
RIVOCERANIBCHEMBL3186534Small moleculePhase 3ClinicalTrials.gov111Drugs and targets
CRIZOTINIBCHEMBL601719Small moleculePhase 2ClinicalTrials.gov111Drugs and targets
FULVESTRANTCHEMBL1358Small moleculePhase 2ClinicalTrials.gov111Drugs and targets
SINTILIMABCHEMBL4297829AntibodyPhase 1/2ClinicalTrials.gov111Drugs and targets

Targets10

The targets ChEMBL's mechanism records give for the disease's drugs, through Open Targets, the most drugs first. A mechanism record says what a drug acts on, not that the target causes the disease.

TargetProteinIts drugs that act on itMechanismsHighest stage of those drugsGene in GenesSource
ALKALK tyrosine kinase receptor1ALK tyrosine kinase receptor inhibitor; EML4-ALK inhibitor; NPM/ALK (Nucleophosmin/ALK tyrosine kinase receptor) inhibitorPhase 2https://conductscience.org/library/genes/238Drugs and targets
EML4EML4-ALK1EML4-ALK inhibitorPhase 2https://conductscience.org/library/genes/27436Drugs and targets
ESR1Estrogen receptor1Estrogen receptor alpha antagonist; Estrogen receptor degraderPhase 2https://conductscience.org/library/genes/2099Drugs and targets
KDRVascular endothelial growth factor receptor 21Vascular endothelial growth factor receptor 2 inhibitorPhase 3https://conductscience.org/library/genes/3791Drugs and targets
METHepatocyte growth factor receptor1Hepatocyte growth factor receptor inhibitorPhase 2https://conductscience.org/library/genes/4233Drugs and targets
MST1RMacrophage-stimulating protein receptor1Macrophage-stimulating protein receptor inhibitorPhase 2https://conductscience.org/library/genes/4486Drugs and targets
NPM1NPM/ALK (Nucleophosmin/ALK tyrosine kinase receptor)1NPM/ALK (Nucleophosmin/ALK tyrosine kinase receptor) inhibitorPhase 2https://conductscience.org/library/genes/4869Drugs and targets
PDCD1Programmed cell death protein 11Programmed cell death protein 1 antagonistPhase 1/2https://conductscience.org/library/genes/5133Drugs and targets
ROS1Proto-oncogene tyrosine-protein kinase ROS1Proto-oncogene tyrosine-protein kinase ROS inhibitorPhase 2https://conductscience.org/library/genes/6098Drugs and targets
TYMSThymidylate synthase1Thymidylate synthase inhibitorPhase 3https://conductscience.org/library/genes/7298Drugs and targets

Trials3

Trials an Open Targets clinical report links to the disease, posted results first, then the largest. A trial is shown when the release's checks confirm its link to the disease and Drugs and targets shows its link to one of the disease's drugs.

TrialTitlePhaseParticipantsResults first postedConditionsDrugsLinked bySource
NCT03620643Crizotinib in Lobular Breast, Diffuse Gastric and Triple Negative Lobular Breast Cancer or CDH1-mutated Solid TumoursPhase 2332025-10-30Lobular Breast Carcinoma, Gastric Cancer, Triple Negative Breast Cancer, CDH1 Gene MutationCRIZOTINIB, FULVESTRANTOpen Targets' reading of its recordClinicalTrials.gov
NCT03355612XELOX Plus Apatinib vs XELOX as Post-operative Chemotherapy in Locally Advanced Gastric Signet Ring CarcinomaPhase 3456Gastric CarcinomaCAPECITABINE, OXALIPLATIN, RIVOCERANIBOpen Targets' reading of its recordClinicalTrials.gov
NCT07025889IBI343 Combined With Sintilimab Plus Chemotherapy in Gastric CancerPhase 1/255Gastric CancerSINTILIMABOpen Targets' reading of its recordClinicalTrials.gov

Comparisons in its trials3

Comparisons Trial comparisons calculated in the trials shown here, most participants first. A comparison in one of these trials does not always compare a treatment for the disease, so read the two groups.

ComparisonGroup 1, with the outcomeGroup 2, with the outcomeParticipantsTrialSource
Crizotinib Oral Capsule [Xalkori] Monotherapy vs Crizotinib Oral Capsule [Xalkori] Plus Fulvestrant Injection: Percentage of Participants With Adverse Events (AEs) and Serious AEs (SAEs)6 of 627 of 2733NCT03620643Trial comparisons
Crizotinib Oral Capsule [Xalkori] Monotherapy vs Crizotinib Oral Capsule [Xalkori] Plus Fulvestrant Injection: deaths from any cause6 of 620 of 2733NCT03620643Trial comparisons
Crizotinib Oral Capsule [Xalkori] Monotherapy vs Crizotinib Oral Capsule [Xalkori] Plus Fulvestrant Injection: serious adverse events4 of 65 of 2733NCT03620643Trial comparisons

Papers from its trials1

The papers the trials shown here list on ClinicalTrials.gov as their results (RESULT) or as drawn from them (DERIVED), results first, newest first.

PMIDListed asTrials listing it
35119530DERIVED1

Source PubMed

Data dates

The date of each source this release read.

Open Targets
2026-09-18
Open Targets
Drug links and their checks, from Drugs and targets
2026-09-18
Drugs and targets
ClinicalTrials.gov, from Trials
2026-11-12
Trials
Comparisons, from Trial comparisons
2026-03-23
Trial comparisons
PubMed, for the checks
2026-11-06
PubMed
MeSH, for the checks
2026-11-10
MeSH

Sources 6

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • NLM's MeSHNLM's terms
  • Open TargetsCC0 1.0
  • PubMedNLM's terms
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • NLM's MeSHNLM's
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PubMedNLM's terms

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this disease from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/diseases/v1/MONDO_0007648

GET https://conductscience.org/api/diseases/v1/MONDO_0007648/drugs