Tenosynovitis
diseaseOn 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
| Field | Value |
|---|---|
| Canonical name | tenosynovitis |
| Mondo ID | MONDO:0004855 |
| EFO | EFO:1001435 |
| MeSH | D013717 |
| DOID | DOID:970 |
| ICD-11 | 163006370 |
| SNOMED CT | 67801009 |
| UMLS | C0039520 |
| MedGen | 52670 |
| 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 disorder › muscle tissue disorder › skeletal muscle disorder › myopathy › myositis disease › tendinitis › tenosynovitis
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
| rsID | p-value | Gene | Risk allele | Odds ratio |
|---|---|---|---|---|
| chr16:69867835 | 3e-24 | A | 0.1 | |
| rs3790086 | 9e-22 | WWP2 | C | 0.08 |
| rs12694411 | 2e-18 | TESHL | T | 0.09 |
| chr2:218146354 | 1e-17 | T | 0.12 | |
| chr7:46034024 | 3e-17 | G | 0.09 | |
| rs11076004 | 9e-13 | FTO | G | 0.07 |
| rs2965069 | 3e-12 | IGFBP3 - FTLP15 | C | 0.07 |
| rs989437 | 6e-12 | CREB5 | A | 0.06 |
| rs7220854 | 1e-11 | RNU7-155P - MYL6P5 | T | 0.07 |
| chr17:69315666 | 2e-11 | C | 0.07 | |
| rs198462 | 2e-09 | MYRF-AS1, MYRF | ? |
Top studies (by case count)
| Study | Lead author | Year | Cases | Controls | Title |
|---|---|---|---|---|---|
| GCST90476242 | Verma A | 2024 | 23,077 | 408,046 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90080520 | Backman JD | 2021 | 8,632 | 371,813 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
| GCST90084506 | Backman JD | 2021 | 8,632 | 371,813 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
| GCST90478948 | Verma A | 2024 | 6,832 | 109,011 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90480517 | Verma A | 2024 | 6,832 | 109,011 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90080524 | Backman JD | 2021 | 5,503 | 375,456 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
| GCST90084510 | Backman JD | 2021 | 5,503 | 375,456 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
| GCST90651333 | Liu TY | 2025 | 3,960 | 210,582 | Diversity and longitudinal records: Genetic architecture of disease associations and polygenic risk in the Taiwanese Han population. |
| GCST90478947 | Verma A | 2024 | 3,748 | 53,173 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90044562 | Jiang L | 2021 | 3,692 | 452,656 | A generalized linear mixed model association tool for biobank-scale data. |
Variant details and genetic-evidence tiers
Tier distribution (top 50 variants)
| Tier | Variants |
|---|---|
| Tier 1: coding | 0 |
| Tier 2: splice/UTR | 0 |
| Tier 3: regulatory | 0 |
| Tier 4: intronic/intergenic | 11 |
MAF distribution
| Bucket | Variants |
|---|---|
| common (>=0.05) | 11 |
| low_freq (0.01-0.05) | 0 |
| rare (<0.01) | 0 |
| unknown | 0 |
Functional consequences
| Consequence | Count |
|---|---|
| intron_variant | 6 |
| unknown | 4 |
| intergenic_variant | 1 |
Top variants
| rsID | Chr | Pos | Alleles | MAF | Consequence | Gene | p-value | Tier |
|---|---|---|---|---|---|---|---|---|
| chr16:69867835 | 0.445 | 3e-24 | Tier 4: intronic/intergenic | |||||
| rs3790086 | 16 | 69853804 | C>A,G,T | 0.442 | intron_variant | WWP2 | 9e-22 | Tier 4: intronic/intergenic |
| rs12694411 | 2 | 217281820 | T>A,C,G | 0.385 | intron_variant | TESHL | 2e-18 | Tier 4: intronic/intergenic |
| chr2:218146354 | 0.151 | 1e-17 | Tier 4: intronic/intergenic | |||||
| chr7:46034024 | 0.34 | 3e-17 | Tier 4: intronic/intergenic | |||||
| rs11076004 | 16 | 53880018 | G>A,C,T | 0.369 | intron_variant | FTO | 9e-13 | Tier 4: intronic/intergenic |
| rs2965069 | 7 | 45978547 | C>T | 0.338 | intron_variant | IGFBP3 - FTLP15 | 3e-12 | Tier 4: intronic/intergenic |
| rs989437 | 7 | 28790881 | A>G | 0.398 | intron_variant | CREB5 | 6e-12 | Tier 4: intronic/intergenic |
| rs7220854 | 17 | 71311858 | T>A,C | 0.333 | intergenic_variant | RNU7-155P - MYL6P5 | 1e-11 | Tier 4: intronic/intergenic |
| chr17:69315666 | 0.37 | 2e-11 | Tier 4: intronic/intergenic | |||||
| rs198462 | 11 | 61756647 | G>A,C,T | 0.05 | intron_variant | MYRF-AS1, MYRF | 2e-09 | Tier 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.
| Drug | Development status |
|---|---|
| Cortisone Acetate | Approved (phase 4) |
| Dexamethasone | Approved (phase 4) |
| Hydrocortisone | Approved (phase 4) |
| Methylprednisolone | Approved (phase 4) |
| Prednisolone | Approved (phase 4) |
| Prednisone | Approved (phase 4) |
| Triamcinolone Acetonide | Approved (phase 4) |
Clinical trials & evidence
Clinical trials
Clinical trials: 9.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 6 |
| PHASE4 | 2 |
| PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT03704584 | PHASE4 | TERMINATED | Corticosteroid(CS) + Lido or Corticosteroid(CS) Alone |
| NCT03792945 | PHASE4 | COMPLETED | Comparison of the Efficacy of Corticosteroid Injection and ESWT in Patients With CTS |
| NCT02266433 | PHASE3 | TERMINATED | Dexamethasone Versus Ketorolac Injection for the Treatment of Local Inflammatory Hand and Upper Extremity Disorders |
| NCT06477965 | Not specified | RECRUITING | Embo Registry; National Registry for Artery Embolization |
| NCT07553910 | Not specified | NOT_YET_RECRUITING | Tenosynovitis in Polyarticular and Oligoarticular Juvenile Idiopathic Arthritis |
| NCT01424995 | Not specified | COMPLETED | The Natural History of Congenital Trigger Thumbs |
| NCT02320929 | Not specified | COMPLETED | The Treatment of Purulent Flexor Tenosynovitis |
| NCT03914235 | Not specified | COMPLETED | Anesthesia Tumescent for Surgical Management of Tenosynovitis. |
| NCT06918158 | Not specified | COMPLETED | Mobilization With Movement Versus Joint-Specific Manipulation in De Quervain’s Tenosynovitis |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| KETOROLAC | 4 | 1 |
Related Atlas pages
- Drugs: Ketorolac