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Disease · MONDO_0008501

Sturge-Weber syndrome

6 sourcesdiseases-2026-09-18-0.1.0

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ConductScience Library. Sturge-Weber syndrome. Diseases, record MONDO_0008501. Release diseases-2026-09-18-0.1.0, 18 Sept 2026. https://conductscience.org/library/diseases/MONDO_0008501

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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
Sturge-Weber syndrome
Open Targets
Open Targets ID
MONDO_0008501
Open Targets
Other names
SWS, Sturge-Weber disease, Sturge-Weber syndrome, somatic, mosaic, Sturge-Weber-Dimitri syndrome, Sturge-Weber-Krabbe angiomatosis, Sturge-Weber-Krabbe syndrome, encephalofacial angiomatosis, encephalotrigeminal angiomatosis, encephalotrigeminal syndrome
Open Targets
Disease Ontology
DOID:0111563
Disease Ontology
MeSH
D013341
MeSH
NCI Thesaurus
C3391
NCI Thesaurus
Orphanet
ORPHA:3205
Orphanet
Highest stage of its drugs
Phase 2, for 2 of its 3 drugs, from ClinicalTrials.gov
Open Targets

Drugs3

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
CANNABIDIOLCHEMBL190461Small moleculePhase 2ClinicalTrials.gov222Drugs and targets
SIROLIMUSCHEMBL413Small moleculePhase 2ClinicalTrials.gov111Drugs and targets
TIMOLOLCHEMBL499Small moleculePhase 1ClinicalTrials.gov111Drugs and targets

Targets4

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
ADRB1Beta-1 adrenergic receptor1Beta-1 adrenergic receptor antagonistPhase 1https://conductscience.org/library/genes/153Drugs and targets
ADRB2Beta-2 adrenergic receptor1Beta-2 adrenergic receptor antagonistPhase 1https://conductscience.org/library/genes/154Drugs and targets
CNR1Cannabinoid receptor 11Cannabinoid CB1 receptor negative allosteric modulatorPhase 2https://conductscience.org/library/genes/1268Drugs and targets
FKBP1APeptidyl-prolyl cis-trans isomerase FKBP1A1FK506-binding protein 1A inhibitorPhase 2https://conductscience.org/library/genes/2280Drugs and targets

Trials4

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
NCT04447846Novel Cognitive Treatment Targets for Epidiolex in Sturge- Weber SyndromePhase 2112023-05-25Sturge-Weber SyndromeCANNABIDIOLIts record names the diseaseClinicalTrials.gov
NCT02332655Cannabidiol Expanded Access Study in Medically Refractory Sturge-Weber SyndromePhase 1/252022-03-02Sturge-Weber SyndromeCANNABIDIOLIts record names the diseaseClinicalTrials.gov
NCT02080624Efficacy and Safety Study of Topical Rapamycin Associated With Pulsed Dye Laser in Patients With Sturge-Weber SyndromePhase 223Sturge- Weber SyndromeSIROLIMUSIts record names the diseaseClinicalTrials.gov
NCT01533376Treatment of Port-wine Mark in Sturge-Weber Syndrome Using Topical TimololPhase 13Sturge Weber Syndrome, Port-wine MarkTIMOLOLIts 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_0008501

GET https://conductscience.org/api/diseases/v1/MONDO_0008501/drugs