Cellulitis
diseaseOn this page
Also known as cellulitis (disease)
Summary
Cellulitis (MONDO:0005230) is a disease with 27 GWAS associations across 74 studies and 72 clinical trials. Top therapeutic interventions include cephalexin anhydrous, vancomycin, and clindamycin. A subtype of vesiculobullous skin disease — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- GWAS associations: 27
- Clinical trials: 72
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | cellulitis |
| Mondo ID | MONDO:0005230 |
| EFO | EFO:0003035 |
| MeSH | D002481 |
| DOID | DOID:3488 |
| NCIT | C26715 |
| SNOMED CT | 128045006 |
| UMLS | C0007642 |
| MedGen | 40174 |
| Is cancer (heuristic) | no |
Also known as: cellulitis · cellulitis (disease)
Data availability: 27 GWAS associations (74 studies) · 1 HPO phenotype.
Disease family
This is a subtype of vesiculobullous skin disease. 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 › integumentary system disorder › skin disorder › vesiculobullous skin disease › cellulitis
Related subtypes (7): herpes zoster, chickenpox, gas gangrene, epidermolysis bullosa, autoimmune bullous skin disease, eosinophilic pustular folliculitis, papular urticaria
Subtypes (3): Ludwig’s angina, orbital cellulitis, anaerobic cellulitis
Genetics & variants
GWAS landscape
27 GWAS associations across 74 studies. Top hits map to 13 distinct genes (as reported by GWAS).
Top associations by p-value
| rsID | p-value | Gene | Risk allele | Odds ratio |
|---|---|---|---|---|
| rs1558902 | 2e-28 | FTO | T | 0.11 |
| rs9927317 | 2e-27 | FTO | C | 0.06 |
| rs62048402 | 3e-25 | FTO | G | 0.11 |
| rs17817712 | 1e-23 | FTO | A | 0.06 |
| chr11:28741136 | 3e-16 | A | 0.05 | |
| chr14:99669005 | 5e-15 | G | 0.05 | |
| chr5:128014857 | 2e-14 | T | 0.07 | |
| chr9:5073770 | 6e-14 | T | 1.03 | |
| rs13107325 | 2e-13 | SLC39A8 | C | 0.07 |
| rs3933088 | 1e-12 | BCL11B | T | 0.04 |
| rs552158554 | 9e-12 | ZNF277-AS1, ZNF277 | G | 2.01 |
| rs545197812 | 2e-11 | NAV1, IPO9-AS1 | G | 3.57 |
| rs546882621 | 3e-11 | IPO4 | G | 3.79 |
| rs189033558 | 3e-11 | BNC1 | G | 2.07 |
| chr6:70380262 | 9e-09 | A | 2.34 | |
| rs35441103 | 1e-08 | TENM2 | ? | |
| chr13:83055968 | 1e-08 | TATATA | 2.37 | |
| chrX:152102444 | 2e-08 | TAG | 1.07 | |
| rs185308479 | 3e-08 | GNAL | ? | |
| chr2:106180298 | 3e-08 | T | 1.39 | |
| rs181428954 | 4e-08 | CDKN2AIPNLP3 - AZU1P1 | ? | |
| rs1308856665 | 1e-07 | AK6P1 - ZNF970P | ? | |
| rs9820329 | 1e-07 | OR7E29P - OR7E93P | ? | |
| rs4537545 | 3e-07 | IL6R | ? | |
| rs74818536 | 4e-07 | BBX | ? | |
| rs62285272 | 7e-07 | PPP4R2P2 - SDHAP1 | ? |
Top studies (by case count)
| Study | Lead author | Year | Cases | Controls | Title |
|---|---|---|---|---|---|
| GCST90476165 | Verma A | 2024 | 72,843 | 328,574 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90473905 | UK Biobank Whole-Genome Sequencing Consortium | 2025 | 31,758 | 426,682 | Whole-genome sequencing of 490,640 UK Biobank participants. |
| GCST90476166 | Verma A | 2024 | 20,317 | 412,161 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90478743 | Verma A | 2024 | 19,518 | 87,520 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90080331 | Backman JD | 2021 | 12,973 | 361,040 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
| GCST90084317 | Backman JD | 2021 | 12,973 | 361,040 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
| GCST90281156 | Hamilton FW | 2023 | 12,196 | 474,288 | Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. |
| GCST90478746 | Verma A | 2024 | 11,729 | 421,230 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90478742 | Verma A | 2024 | 9,091 | 44,352 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90436569 | Zhou W | 2018 | 7,451 | 397,635 | Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies. |
Variant details and genetic-evidence tiers
Tier distribution (top 50 variants)
| Tier | Variants |
|---|---|
| Tier 1: coding | 1 |
| Tier 2: splice/UTR | 2 |
| Tier 3: regulatory | 0 |
| Tier 4: intronic/intergenic | 23 |
MAF distribution
| Bucket | Variants |
|---|---|
| common (>=0.05) | 12 |
| low_freq (0.01-0.05) | 0 |
| rare (<0.01) | 4 |
| unknown | 10 |
Functional consequences
| Consequence | Count |
|---|---|
| intron_variant | 13 |
| unknown | 8 |
| 3_prime_UTR_variant | 2 |
| intergenic_variant | 2 |
| missense_variant | 1 |
Top variants
| rsID | Chr | Pos | Alleles | MAF | Consequence | Gene | p-value | Tier |
|---|---|---|---|---|---|---|---|---|
| rs1558902 | 16 | 53769662 | T>A | 0.403 | intron_variant | FTO | 2e-28 | Tier 4: intronic/intergenic |
| rs9927317 | 16 | 53787084 | C>A,G,T | 0.393 | intron_variant | FTO | 2e-27 | Tier 4: intronic/intergenic |
| rs62048402 | 16 | 53769311 | G>A,T | 0.33 | intron_variant | FTO | 3e-25 | Tier 4: intronic/intergenic |
| rs17817712 | 16 | 53787213 | A>G,T | 0.322 | intron_variant | FTO | 1e-23 | Tier 4: intronic/intergenic |
| chr11:28741136 | 0.439 | 3e-16 | Tier 4: intronic/intergenic | |||||
| chr14:99669005 | 0.331 | 5e-15 | Tier 4: intronic/intergenic | |||||
| chr5:128014857 | 2e-14 | Tier 4: intronic/intergenic | ||||||
| chr9:5073770 | 6e-14 | Tier 4: intronic/intergenic | ||||||
| rs13107325 | 4 | 102267552 | C>A,T | 0.083 | missense_variant | SLC39A8 | 2e-13 | Tier 1: coding |
| rs3933088 | 14 | 99238994 | T>A,C | 0.364 | intron_variant | BCL11B | 1e-12 | Tier 4: intronic/intergenic |
| rs552158554 | 7 | 112344066 | G>A,C | 0.001 | 3_prime_UTR_variant | ZNF277-AS1, ZNF277 | 9e-12 | Tier 2: splice/UTR |
| rs545197812 | 1 | 201713642 | G>A | 0 | intron_variant | NAV1, IPO9-AS1 | 2e-11 | Tier 4: intronic/intergenic |
| rs546882621 | 14 | 24184451 | G>A,T | 0 | intron_variant | IPO4 | 3e-11 | Tier 4: intronic/intergenic |
| rs189033558 | 15 | 83273180 | G>T | 0.001 | intron_variant | BNC1 | 3e-11 | Tier 4: intronic/intergenic |
| chr6:70380262 | 9e-09 | Tier 4: intronic/intergenic | ||||||
| rs35441103 | 5 | 167330512 | C>A,G,T | 0.05 | intron_variant | TENM2 | 1e-08 | Tier 4: intronic/intergenic |
| chr13:83055968 | 1e-08 | Tier 4: intronic/intergenic | ||||||
| chrX:152102444 | 2e-08 | Tier 4: intronic/intergenic | ||||||
| rs185308479 | 18 | 11882491 | T>G | 3_prime_UTR_variant | GNAL | 3e-08 | Tier 2: splice/UTR | |
| chr2:106180298 | 3e-08 | Tier 4: intronic/intergenic | ||||||
| rs181428954 | 13 | 39854242 | C>T | intron_variant | CDKN2AIPNLP3 - AZU1P1 | 4e-08 | Tier 4: intronic/intergenic | |
| rs1308856665 | 12 | 34713888 | C>A,G | intergenic_variant | AK6P1 - ZNF970P | 1e-07 | Tier 4: intronic/intergenic | |
| rs9820329 | 3 | 125713674 | G>A,C | 0.05 | intergenic_variant | OR7E29P - OR7E93P | 1e-07 | Tier 4: intronic/intergenic |
| rs4537545 | 1 | 154446403 | C>T | 0.05 | intron_variant | IL6R | 3e-07 | Tier 4: intronic/intergenic |
| rs74818536 | 3 | 107574707 | T>C | intron_variant | BBX | 4e-07 | Tier 4: intronic/intergenic | |
| rs62285272 | 3 | 195943607 | C>A,T | 0.05 | intron_variant | PPP4R2P2 - SDHAP1 | 7e-07 | 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
0 approved, 6 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.
| Drug | Development status |
|---|---|
| Cefazolin | Phase 3 (in late-stage trials) |
| Dalbavancin | Phase 3 (in late-stage trials) |
| Floxacillin | Phase 3 (in late-stage trials) |
| Linezolid | Phase 3 (in late-stage trials) |
| Moxifloxacin | Phase 3 (in late-stage trials) |
| Vancomycin | Phase 3 (in late-stage trials) |
Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Probenecid.
Clinical trials & evidence
Clinical trials
Clinical trials: 72.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 43 |
| PHASE4 | 11 |
| PHASE3 | 8 |
| PHASE2 | 7 |
| PHASE2/PHASE3 | 2 |
| PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05852262 | PHASE4 | ENROLLING_BY_INVITATION | High-dose Cephalexin for Cellulitis (HI-DOCC) |
| NCT07532941 | PHASE4 | NOT_YET_RECRUITING | Clinical Efficacy of Stopping Oral Antibiotics When Symptoms Stop, Compared to ‘Finishing the Course’ |
| NCT00295178 | PHASE4 | COMPLETED | Study Comparing CUBICIN® (Daptomycin for Injection) With Vancomycin in Cellulitis or Erysipelas |
| NCT00552799 | PHASE4 | COMPLETED | RCT to Investigate if Prophylactic Antibiotics Prevent Further Episodes of Cellulitis (Erysipelas) of the Leg |
| NCT00746109 | PHASE4 | COMPLETED | Study of Wound Packing After Superficial Skin Abscess Drainage |
| NCT01549613 | PHASE4 | COMPLETED | Evaluation of Daptomycin for the Emergency Department Treatment of Complicated Skin and Skin Structure Infections |
| NCT01626560 | PHASE4 | COMPLETED | The Effects of Daptomycin and Cytokines Production in Comparison With Vancomycin |
| NCT01876628 | PHASE4 | COMPLETED | Adjunctive Clindamycin for Cellulitis: C4C Trial. |
| NCT02032654 | PHASE4 | TERMINATED | Duration of ANtibiotic Therapy for CEllulitis |
| NCT02922686 | PHASE4 | UNKNOWN | Penicillin for the Emergency Department Outpatient Treatment of CELLulitis |
| NCT04471246 | PHASE4 | COMPLETED | High-dose vs. Standard-dose Cephalexin for Cellulitis |
| NCT00257036 | PHASE2/PHASE3 | COMPLETED | A Study of the Safety and Effectiveness of Oral Levofloxacin Compared With Oral Ciprofloxacin in the Treatment of Adults With Mild to Moderate Infections of the Skin and the Supportive Layers Beneath the Skin |
| NCT00323219 | PHASE3 | COMPLETED | Oral Moxifloxacin Versus Cefazolin and Oral Probenecid in the Management of Skin and Soft Tissue Infections in the Emergency Department |
| NCT00619710 | PHASE3 | COMPLETED | Complicated Skin and Skin Structure Infections |
| NCT01085929 | PHASE3 | COMPLETED | Incision and Drainage Versus Needle Aspiration in Soft Tissue Abscesses |
| NCT01252719 | PHASE3 | COMPLETED | Oritavancin Versus IV Vancomycin for the Treatment of Participants With Acute Bacterial Skin and Skin Structure Infection (SOLO I) |
| NCT01252732 | PHASE3 | COMPLETED | Oritavancin Versus IV Vancomycin for the Treatment of Patients With Acute Bacterial Skin and Skin Structure Infection |
| NCT01339091 | PHASE3 | COMPLETED | Efficacy and Safety of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections |
| NCT01431339 | PHASE3 | COMPLETED | Efficacy and Safety of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections |
| NCT02127970 | PHASE3 | COMPLETED | Single Dose vs. Two Dose Regimen of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections |
| NCT03556917 | PHASE2/PHASE3 | COMPLETED | The Effects of Iontophoresis in Women With Gynoid Hidrolipodystrophy. |
| NCT00061633 | PHASE2 | COMPLETED | Phase 2 Trial of TD 6424 (Telavancin) Versus Standard Therapy for Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI) |
| NCT00514527 | PHASE2 | COMPLETED | A Study for Patients With Complicated Skin and Skin Structure Infections |
| NCT00893048 | PHASE2 | WITHDRAWN | The Use of Oral Steroids in the Treatment of Cellulitis |
| NCT00984022 | PHASE2 | COMPLETED | Aquacel Versus Iodoform Gauze for Filling Abscess Cavity Following Incision and Drainage |
| NCT01029782 | PHASE2 | COMPLETED | Comparison of Intravenous Cefazolin Plus Oral Probenecid With Oral Cephalexin for the Treatment of Cellulitis |
| NCT01519492 | PHASE2 | COMPLETED | A Study of Safety, Tolerability, and Efficacy of AFN-12520000 in the Treatment of Acute Bacterial Skin and Skin Structure Infections Due to Staphylococci |
| NCT01519778 | PHASE2 | COMPLETED | A Phase 2 Safety and Exploratory Skin Lesion Measurement of TR-701 FA Study |
| NCT01557426 | PHASE1 | COMPLETED | Soft Tissue Ultrasound of Infections |
| NCT06715306 | Not specified | RECRUITING | Intravenous Versus Oral Treatment of the Main Acute Infections |
| NCT07093749 | Not specified | RECRUITING | Perspectives on Antibiotics and Tracking Symptoms in Children |
| NCT07492030 | Not specified | NOT_YET_RECRUITING | Validation of the Use of the Arteriovenous Tension Difference in CO2 Under Hyperbaric Conditions |
| NCT00139100 | Not specified | COMPLETED | Evaluation of Antibacterial Soap for Treatment of Lymphedema in a Filariasis-Endemic Area |
| NCT00289588 | Not specified | COMPLETED | An Attempt to Reduce Community-Acquired Methicillin-Resistant Staphylococcus Aureus (MRSA) Infection in Soldiers |
| NCT00489021 | Not specified | UNKNOWN | Feasibility and Outcomes of Older Patients Hospitalization |
| NCT00636025 | Not specified | COMPLETED | Cellulite and Magnetic Resonance Imaging |
| NCT00676130 | Not specified | COMPLETED | Study of New Antibiotic Regimen for the Treatment of Uncomplicated Cellulitis in Emergency Department Patients |
| NCT00714402 | Not specified | COMPLETED | Procalcitonin Level and Kinetics in Children With Bacterial Infections |
| NCT00737269 | Not specified | COMPLETED | A Complicated Skin and Soft-tissue Infection Patient Registry |
| NCT01238276 | Not specified | NO_LONGER_AVAILABLE | Direct Antibiotic Delivery of Cefazolin Into Soft Tissue Infections Using Subcutaneous Injection and Ultrasonic Dispersion |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| CEPHALEXIN ANHYDROUS | 4 | 12 |
| VANCOMYCIN | 4 | 5 |
| CLINDAMYCIN | 4 | 3 |
| DAPTOMYCIN | 4 | 3 |
| PENICILLIN V | 4 | 3 |
| CEFAZOLIN | 4 | 2 |
| DALBAVANCIN | 4 | 2 |
| LEVOFLOXACIN ANHYDROUS | 4 | 2 |
| LINEZOLID | 4 | 2 |
| CAFFEINE | 4 | 1 |
| CEFTOLOZANE | 4 | 1 |
| MEROPENEM | 4 | 1 |
| MOXIFLOXACIN | 4 | 1 |
| MUPIROCIN | 4 | 1 |
| OFLOXACIN | 4 | 1 |
| ORITAVANCIN | 4 | 1 |
| TELAVANCIN | 4 | 1 |
| FLOXACILLIN | 3 | 4 |
| CEPHALOSPORIN | 3 | 1 |
| CHEMBL1649722 | 0 | 3 |
| CHEMBL4286784 | 0 | 3 |
| CHEMBL4299436 | 0 | 3 |
| CHEMBL4744444 | 0 | 3 |
| CHEMBL4778239 | 0 | 2 |
| CHEMBL4785392 | 0 | 2 |
| CHEMBL6174705 | 0 | 2 |
| CHEMBL4802121 | 0 | 1 |
| CHEMBL5271499 | 0 | 1 |
| CHEMBL4793658 | 0 | 1 |
| PARAXANTHINE | 0 | 1 |