Tenosynovitis

disease
On this page

Also known as tendon sheath inflammationTenosynovitides

Summary

Tenosynovitis (MONDO:0004855) is a disease with 12 GWAS associations across 17 studies and 9 clinical trials. Top therapeutic interventions include ketorolac. A subtype of tendinitis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • GWAS associations: 12
  • Clinical trials: 9

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nametenosynovitis
Mondo IDMONDO:0004855
EFOEFO:1001435
MeSHD013717
DOIDDOID:970
ICD-11163006370
SNOMED CT67801009
UMLSC0039520
MedGen52670
Is cancer (heuristic)no

Also known as: tendon sheath inflammation · Tenosynovitides

Data availability: 12 GWAS associations (17 studies).

Disease family

This is a subtype of tendinitis. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › musculoskeletal system disordermuscle tissue disorderskeletal muscle disordermyopathymyositis diseasetendinitistenosynovitis

Related subtypes (5): patellar tendinitis, tibialis tendinitis, Achilles bursitis, calcific tendinitis, paratenonitis

Subtypes (2): bicipital tenosynovitis, tenosynovitis of foot and ankle

Genetics & variants

GWAS landscape

12 GWAS associations across 17 studies. Top hits map to 6 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
chr16:698678353e-24A0.1
rs37900869e-22WWP2C0.08
rs126944112e-18TESHLT0.09
chr2:2181463541e-17T0.12
chr7:460340243e-17G0.09
rs110760049e-13FTOG0.07
rs29650693e-12IGFBP3 - FTLP15C0.07
rs9894376e-12CREB5A0.06
rs72208541e-11RNU7-155P - MYL6P5T0.07
chr17:693156662e-11C0.07
rs1984622e-09MYRF-AS1, MYRF?

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90476242Verma A202423,077408,046Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90080520Backman JD20218,632371,813Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90084506Backman JD20218,632371,813Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90478948Verma A20246,832109,011Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90480517Verma A20246,832109,011Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90080524Backman JD20215,503375,456Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90084510Backman JD20215,503375,456Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90651333Liu TY20253,960210,582Diversity and longitudinal records: Genetic architecture of disease associations and polygenic risk in the Taiwanese Han population.
GCST90478947Verma A20243,74853,173Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90044562Jiang L20213,692452,656A generalized linear mixed model association tool for biobank-scale data.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding0
Tier 2: splice/UTR0
Tier 3: regulatory0
Tier 4: intronic/intergenic11

MAF distribution

BucketVariants
common (>=0.05)11
low_freq (0.01-0.05)0
rare (<0.01)0
unknown0

Functional consequences

ConsequenceCount
intron_variant6
unknown4
intergenic_variant1

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
chr16:698678350.4453e-24Tier 4: intronic/intergenic
rs37900861669853804C>A,G,T0.442intron_variantWWP29e-22Tier 4: intronic/intergenic
rs126944112217281820T>A,C,G0.385intron_variantTESHL2e-18Tier 4: intronic/intergenic
chr2:2181463540.1511e-17Tier 4: intronic/intergenic
chr7:460340240.343e-17Tier 4: intronic/intergenic
rs110760041653880018G>A,C,T0.369intron_variantFTO9e-13Tier 4: intronic/intergenic
rs2965069745978547C>T0.338intron_variantIGFBP3 - FTLP153e-12Tier 4: intronic/intergenic
rs989437728790881A>G0.398intron_variantCREB56e-12Tier 4: intronic/intergenic
rs72208541771311858T>A,C0.333intergenic_variantRNU7-155P - MYL6P51e-11Tier 4: intronic/intergenic
chr17:693156660.372e-11Tier 4: intronic/intergenic
rs1984621161756647G>A,C,T0.05intron_variantMYRF-AS1, MYRF2e-09Tier 4: intronic/intergenic

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

Drugs indicated for this disease

7 approved. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.

DrugDevelopment status
Cortisone AcetateApproved (phase 4)
DexamethasoneApproved (phase 4)
HydrocortisoneApproved (phase 4)
MethylprednisoloneApproved (phase 4)
PrednisoloneApproved (phase 4)
PrednisoneApproved (phase 4)
Triamcinolone AcetonideApproved (phase 4)

Clinical trials & evidence

Clinical trials

Clinical trials: 9.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified6
PHASE42
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03704584PHASE4TERMINATEDCorticosteroid(CS) + Lido or Corticosteroid(CS) Alone
NCT03792945PHASE4COMPLETEDComparison of the Efficacy of Corticosteroid Injection and ESWT in Patients With CTS
NCT02266433PHASE3TERMINATEDDexamethasone Versus Ketorolac Injection for the Treatment of Local Inflammatory Hand and Upper Extremity Disorders
NCT06477965Not specifiedRECRUITINGEmbo Registry; National Registry for Artery Embolization
NCT07553910Not specifiedNOT_YET_RECRUITINGTenosynovitis in Polyarticular and Oligoarticular Juvenile Idiopathic Arthritis
NCT01424995Not specifiedCOMPLETEDThe Natural History of Congenital Trigger Thumbs
NCT02320929Not specifiedCOMPLETEDThe Treatment of Purulent Flexor Tenosynovitis
NCT03914235Not specifiedCOMPLETEDAnesthesia Tumescent for Surgical Management of Tenosynovitis.
NCT06918158Not specifiedCOMPLETEDMobilization With Movement Versus Joint-Specific Manipulation in De Quervain’s Tenosynovitis

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
KETOROLAC41