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Disease · MONDO_0021541

hemangioma of retina

6 sourcesdiseases-2026-09-18-0.1.0

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ConductScience Library. hemangioma of retina. Diseases, record MONDO_0021541. Release diseases-2026-09-18-0.1.0, 18 Sept 2026. https://conductscience.org/library/diseases/MONDO_0021541

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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
hemangioma of retina
Open Targets
Open Targets ID
MONDO_0021541
Open Targets
Other names
angioma of retina, angioma of the retina, hemangioma of the retina, retina angioma, retina hemangioma, retinal angioma, retinal hemangioma
Open Targets
NCI Thesaurus
C3634
NCI Thesaurus
Highest stage of its drugs
Phase 1/2, for 1 of its 2 drugs, from ClinicalTrials.gov
Open Targets

Drugs2

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
SUNITINIB MALATECHEMBL1567Small moleculePhase 1/2ClinicalTrials.gov111Drugs and targets
PEGAPTANIB SODIUMCHEMBL1201421Small moleculePhase 1ClinicalTrials.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
CSF1RMacrophage colony-stimulating factor 1 receptor1Macrophage colony stimulating factor receptor inhibitorPhase 1/2https://conductscience.org/library/genes/1436Drugs and targets
FLT1Vascular endothelial growth factor receptor1Vascular endothelial growth factor receptor inhibitorPhase 1/2https://conductscience.org/library/genes/2321Drugs and targets
FLT3Receptor-type tyrosine-protein kinase FLT31Tyrosine-protein kinase receptor FLT3 inhibitorPhase 1/2https://conductscience.org/library/genes/2322Drugs and targets
FLT4Vascular endothelial growth factor receptor1Vascular endothelial growth factor receptor inhibitorPhase 1/2https://conductscience.org/library/genes/2324Drugs and targets
KDRVascular endothelial growth factor receptor1Vascular endothelial growth factor receptor inhibitorPhase 1/2https://conductscience.org/library/genes/3791Drugs and targets
KITMast/stem cell growth factor receptor Kit1Stem cell growth factor receptor inhibitorPhase 1/2https://conductscience.org/library/genes/3815Drugs and targets
PDGFRAPlatelet-derived growth factor receptor1Platelet-derived growth factor receptor inhibitorPhase 1/2https://conductscience.org/library/genes/5156Drugs and targets
PDGFRBPlatelet-derived growth factor receptor1Platelet-derived growth factor receptor inhibitorPhase 1/2https://conductscience.org/library/genes/5159Drugs and targets
RETProto-oncogene tyrosine-protein kinase receptor Ret1Tyrosine-protein kinase receptor RET inhibitorPhase 1/2https://conductscience.org/library/genes/5979Drugs and targets
VEGFAVascular endothelial growth factor A, long form1Vascular endothelial growth factor A antagonistPhase 1https://conductscience.org/library/genes/7422Drugs and targets

Trials2

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
NCT00673816Sunitinib Malate to Treat Advanced Eye Disease in Patients With Von Hippel-Lindau SyndromePhase 1/222011-12-19Von Hippel-Lindau SyndromeSUNITINIB MALATEIts record names the diseaseClinicalTrials.gov
NCT00056199EYE001 to Treat Retinal Tumors in Patients With Von Hippel-Lindau SyndromePhase 15Hippel-Lindau DiseasePEGAPTANIB SODIUMIts record names the diseaseClinicalTrials.gov

Comparisons in its trials0

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.

None in this release.

Papers from its trials0

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

None in this release.

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_0021541

GET https://conductscience.org/api/diseases/v1/MONDO_0021541/drugs