Rhinitis
diseaseOn this page
Also known as inflammation of nasal cavity mucosanasal cavity mucosa inflammation
Summary
Rhinitis (MONDO:0003014) is a disease with 74 GWAS associations across 16 studies and 108 clinical trials. Top therapeutic interventions include levocetirizine, montelukast, and pseudoephedrine. A subtype of nasal cavity disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- GWAS associations: 74
- Clinical trials: 108
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | rhinitis |
| Mondo ID | MONDO:0003014 |
| EFO | EFO:0008521 |
| MeSH | D012220 |
| DOID | DOID:4483 |
| ICD-10-CM | J30 |
| NCIT | C34986 |
| SNOMED CT | 70076002 |
| UMLS | C0035455 |
| MedGen | 19782 |
| Is cancer (heuristic) | no |
Also known as: inflammation of nasal cavity mucosa · nasal cavity mucosa inflammation
Data availability: 74 GWAS associations (16 studies).
Disease family
An umbrella term covering 3 Mondo subtypes.
Classification path: disease › human disease › disease by body system or component › otorhinolaryngologic disease › nasal disorder › nasal cavity disorder › rhinitis
Related subtypes (4): nasal cavity neoplasm, nasal cavity polyp, Binder syndrome, choanal atresia
Subtypes (3): chronic rhinitis, atrophic rhinitis, allergic rhinitis
Genetics & variants
GWAS landscape
74 GWAS associations across 16 studies. Top hits map to 3 distinct genes (as reported by GWAS).
Top associations by p-value
| rsID | p-value | Gene | Risk allele | Odds ratio |
|---|---|---|---|---|
| chr4:38797027 | 4e-45 | A | 0.12 | |
| chr11:76582682 | 5e-36 | T | 0.09 | |
| chr5:111131801 | 7e-36 | T | 0.09 | |
| chr6:32647680 | 7e-35 | C | 0.11 | |
| chr2:241759225 | 3e-30 | A | 0.09 | |
| rs1438673 | 2e-26 | WDR36 - RPS3AP21 | ? | 1.1 |
| chr2:102318514 | 4e-25 | T | 0.1 | |
| chr9:6209697 | 1e-23 | G | 0.08 | |
| chr4:122307977 | 3e-23 | T | 0.07 | |
| chr5:35851729 | 3e-23 | T | 0.08 | |
| chr16:11127430 | 6e-22 | G | 0.08 | |
| chrX:1243320 | 1e-20 | A | 0.09 | |
| chr15:67157967 | 2e-20 | G | 0.07 | |
| chr17:40608272 | 4e-20 | A | 0.2 | |
| rs2095044 | 2e-19 | RANBP6 - GTF3AP1 | ? | 0.97 |
| chr17:4618178 | 8e-19 | A | 0.23 | |
| chr2:8302417 | 3e-17 | A | 0.06 | |
| chr2:198027075 | 3e-14 | T | 0.05 | |
| rs11406702 | 4e-14 | CFAP144P2 - IL1RL1 | ? | 0.9 |
| chr15:60776978 | 6e-14 | C | 0.07 | |
| chr20:47057814 | 2e-13 | AG | 0.06 | |
| rs2381416 | 6e-13 | RANBP6 - GTF3AP1 | ? | 1.08 |
| chr19:33235671 | 7e-13 | A | 0.1 | |
| chr10:9010183 | 1e-12 | G | 0.05 | |
| chrX:155858365 | 3e-12 | A | 0.07 | |
| chr8:127765473 | 5e-12 | G | 0.05 | |
| chr1:161215268 | 5e-12 | T | 0.05 | |
| rs11236795 | 6e-12 | EMSY - LINC02757 | ? | 0.93 |
| chr11:118872577 | 9e-12 | A | 0.06 | |
| chrX:49264507 | 1e-11 | CTAT | 0.04 |
Top studies (by case count)
| Study | Lead author | Year | Cases | Controls | Title |
|---|---|---|---|---|---|
| GCST90473684 | UK Biobank Whole-Genome Sequencing Consortium | 2025 | 46,689 | 411,751 | Whole-genome sequencing of 490,640 UK Biobank participants. |
| GCST90667965 | UK Biobank Whole-Genome Sequencing Consortium | 2025 | 46,689 | 411,751 | Whole-genome sequencing of 490,640 UK Biobank participants. |
| GCST90726638 | Kim HI | 2026 | 12,560 | 31,466 | Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity. |
| GCST90269782 | Saarentaus EC | 2023 | 8,975 | 199,208 | Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. |
| GCST90269787 | Saarentaus EC | 2023 | 8,975 | 199,208 | Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. |
| GCST90473686 | UK Biobank Whole-Genome Sequencing Consortium | 2025 | 6,563 | 451,877 | Whole-genome sequencing of 490,640 UK Biobank participants. |
| GCST90080106 | Backman JD | 2021 | 3,154 | 376,940 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
| GCST90084092 | Backman JD | 2021 | 3,154 | 376,940 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
| GCST90080105 | Backman JD | 2021 | 1,949 | 382,383 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
| GCST90084091 | Backman JD | 2021 | 1,949 | 382,383 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
Variant details and genetic-evidence tiers
Tier distribution (top 50 variants)
| Tier | Variants |
|---|---|
| Tier 1: coding | 0 |
| Tier 2: splice/UTR | 1 |
| Tier 3: regulatory | 0 |
| Tier 4: intronic/intergenic | 49 |
MAF distribution
| Bucket | Variants |
|---|---|
| common (>=0.05) | 9 |
| low_freq (0.01-0.05) | 0 |
| rare (<0.01) | 0 |
| unknown | 41 |
Functional consequences
| Consequence | Count |
|---|---|
| unknown | 41 |
| intergenic_variant | 5 |
| intron_variant | 3 |
| splice_polypyrimidine_tract_variant | 1 |
Top variants
| rsID | Chr | Pos | Alleles | MAF | Consequence | Gene | p-value | Tier |
|---|---|---|---|---|---|---|---|---|
| chr4:38797027 | 4e-45 | Tier 4: intronic/intergenic | ||||||
| chr11:76582682 | 5e-36 | Tier 4: intronic/intergenic | ||||||
| chr5:111131801 | 7e-36 | Tier 4: intronic/intergenic | ||||||
| chr6:32647680 | 7e-35 | Tier 4: intronic/intergenic | ||||||
| chr2:241759225 | 3e-30 | Tier 4: intronic/intergenic | ||||||
| rs1438673 | 5 | 111131801 | C>A,G,T | 0.05 | intergenic_variant | WDR36 - RPS3AP21 | 2e-26 | Tier 4: intronic/intergenic |
| chr2:102318514 | 4e-25 | Tier 4: intronic/intergenic | ||||||
| chr9:6209697 | 1e-23 | Tier 4: intronic/intergenic | ||||||
| chr4:122307977 | 3e-23 | Tier 4: intronic/intergenic | ||||||
| chr5:35851729 | 3e-23 | Tier 4: intronic/intergenic | ||||||
| chr16:11127430 | 6e-22 | Tier 4: intronic/intergenic | ||||||
| chrX:1243320 | 1e-20 | Tier 4: intronic/intergenic | ||||||
| chr15:67157967 | 2e-20 | Tier 4: intronic/intergenic | ||||||
| chr17:40608272 | 4e-20 | Tier 4: intronic/intergenic | ||||||
| rs2095044 | 9 | 6192796 | T>A,C,G | 0.05 | intergenic_variant | RANBP6 - GTF3AP1 | 2e-19 | Tier 4: intronic/intergenic |
| chr17:4618178 | 8e-19 | Tier 4: intronic/intergenic | ||||||
| chr2:8302417 | 3e-17 | Tier 4: intronic/intergenic | ||||||
| chr2:198027075 | 3e-14 | Tier 4: intronic/intergenic | ||||||
| rs11406702 | 2 | 102299507 | AT>A,ATT | 0.05 | intron_variant | CFAP144P2 - IL1RL1 | 4e-14 | Tier 4: intronic/intergenic |
| chr15:60776978 | 6e-14 | Tier 4: intronic/intergenic | ||||||
| chr20:47057814 | 2e-13 | Tier 4: intronic/intergenic | ||||||
| rs2381416 | 9 | 6193455 | C>A,G,T | 0.05 | intergenic_variant | RANBP6 - GTF3AP1 | 6e-13 | Tier 4: intronic/intergenic |
| chr19:33235671 | 7e-13 | Tier 4: intronic/intergenic | ||||||
| chr10:9010183 | 1e-12 | Tier 4: intronic/intergenic | ||||||
| chrX:155858365 | 3e-12 | Tier 4: intronic/intergenic | ||||||
| chr8:127765473 | 5e-12 | Tier 4: intronic/intergenic | ||||||
| chr1:161215268 | 5e-12 | Tier 4: intronic/intergenic | ||||||
| rs11236795 | 11 | 76585239 | T>A,C,G | 0.05 | intergenic_variant | EMSY - LINC02757 | 6e-12 | Tier 4: intronic/intergenic |
| chr11:118872577 | 9e-12 | Tier 4: intronic/intergenic | ||||||
| chrX:49264507 | 1e-11 | 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
2 approved, 7 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.
| Drug | Development status |
|---|---|
| Flunisolide | Approved (phase 4) |
| Omalizumab | Approved (phase 4) |
| Diphenhydramine | Phase 3 (in late-stage trials) |
| Dropropizine | Phase 3 (in late-stage trials) |
| Fluticasone Furoate | Phase 3 (in late-stage trials) |
| Levocetirizine | Phase 3 (in late-stage trials) |
| Pseudoephedrine | Phase 3 (in late-stage trials) |
| Sodium Chloride | Phase 3 (in late-stage trials) |
| Triamcinolone Acetonide | Phase 3 (in late-stage trials) |
Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Cetirizine, Fluticasone Propionate, Onabotulinumtoxina.
Clinical trials & evidence
Clinical trials
Clinical trials: 108.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 53 |
| PHASE3 | 20 |
| PHASE2 | 15 |
| PHASE4 | 12 |
| PHASE1 | 5 |
| PHASE2/PHASE3 | 2 |
| PHASE1/PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00406094 | PHASE4 | UNKNOWN | Singulair Use in Non-Allergic Rhinitis Eosinophil Syndrome (NARES) |
| NCT00521131 | PHASE4 | COMPLETED | Evaluation of Efficacy and Safety of Levocetirizine to Subjects With Perennial Allergic Rhinitis to House Dust Mites |
| NCT00630474 | PHASE4 | COMPLETED | Nasal Decongestion and Obstructive Sleep Apnea |
| NCT00822406 | PHASE4 | COMPLETED | Effectiveness of Individualized Homeopathic Treatment in Perennial Allergic Rhinitis |
| NCT00963573 | PHASE4 | COMPLETED | Efficacy & Safety of Loratadine-Betamethasone Oral Solution for Treatment of Severe Perennial Allergic Rhinitis in Children (Study P03428) |
| NCT01118312 | PHASE4 | COMPLETED | Study of Asthma and Nasal Steroids |
| NCT01469234 | PHASE4 | COMPLETED | A Study of Onset of Action of Loratadine and Fexofenadine in Participants With Seasonal Allergic Rhinitis (P08712) |
| NCT01862523 | PHASE4 | COMPLETED | Mechanisms of Capsaicin Treatment in Idiopathic Rhinitis Patients and Controls |
| NCT02278081 | PHASE4 | UNKNOWN | The Relationship Between Gastroesophageal Reflux and Pediatric Rhinitis: Significance of Pale/Blue Colored Turbinate |
| NCT02477293 | PHASE4 | COMPLETED | The Efficacy and Safety of Hyeonggaeyeongyo-tang for Chronic Rhinitis According to Pattern Identification in Korean Medicine |
| NCT04132570 | PHASE4 | COMPLETED | A Study of Intranasal Budesonide Aqueous Spray for Treatment of Rhinitis During Periods of High Airborne Pollution |
| NCT06448585 | PHASE4 | COMPLETED | Dietary Supplement (Beta-Glucans) in Allergic Patients Undergoing Subcutaneous Immunotherapy. |
| NCT07348302 | PHASE3 | RECRUITING | Efficacy and Safety of SLIT in Patients With Rhinitis/RC With/Without Mild-moderate Asthma, Due to Dpt and/or Df |
| NCT00279916 | PHASE3 | COMPLETED | Short Term Relief of Eustachian Tube Dysfunction and Serous Otitis Media Using Intranasal Steroid Sprays |
| NCT00344942 | PHASE3 | TERMINATED | Efficacy and Safety Study of Nasacort in Chronic Non Allergic and Non Infectious Rhinitis in Adults |
| NCT00524836 | PHASE3 | COMPLETED | Efficacy and Safety of Levocetirizine Versus Loratadine for the Treatment of Perennial Allergic Rhinitis |
| NCT00525278 | PHASE3 | COMPLETED | To Evaluate the Efficacy and Safety of Levocetirizine Versus Loratadine for Treatment of Seasonal Allergic Rhinitis |
| NCT00550550 | PHASE3 | COMPLETED | Efficacy and Safety of Grass Sublingual Tablet in Children and Adolescents (P05239 AM3)(COMPLETED) |
| NCT00562159 | PHASE3 | COMPLETED | Efficacy and Safety of Grass Sublingual Tablet in Adults (P05238 AM3)(COMPLETED) |
| NCT00623701 | PHASE3 | COMPLETED | Efficacy and Safety From a High-dosed Sublingual Grass Pollen Preparation |
| NCT00704496 | PHASE3 | COMPLETED | The Effect of Pseudoephedrine on Rhinitis and Sleep |
| NCT00831025 | PHASE3 | COMPLETED | Subcutaneous Immunotherapy Treatment for Patients With Hypersensitivity to Olea Europaea Pollen |
| NCT01096615 | PHASE3 | COMPLETED | Effect Of Probiotic Lactobacillus Paracasei Lp-33 For The Management Of Rhinitis In People Sensitized To Allergens |
| NCT01177852 | PHASE3 | WITHDRAWN | Evaluation of Efficacy and Safety in Control Cough and the Relief of Nasal Symptoms in Children 2-12 Years Old,Suffering From Cough and Acute Rhinitis |
| NCT01248325 | PHASE3 | UNKNOWN | A Study of Luffa Operculate Nasal Solution 5mg/mL Compared With Saline (NaCl 09%) for the Relief of Nasal Obstruction |
| NCT01393548 | PHASE3 | COMPLETED | Efficacy and Safety of Combination of Brompheniramine and Phenylephrine for the Symptoms Relief of Rhinitis |
| NCT01393561 | PHASE3 | COMPLETED | Efficacy and Safety of Combination of Brompheniramine and Phenylephrine for the Symptoms Relief of Rhinitis |
| NCT01563081 | PHASE3 | COMPLETED | Safety Study of Levocetirizine Oral Solution for Japanese Pediatrics |
| NCT01622231 | PHASE3 | COMPLETED | Study FFR116365, an Open-label Study of GW685698X in Paediatric Subjects With Perennial Allergic Rhinitis |
| NCT02272101 | PHASE3 | COMPLETED | Rhinitis in the Elderly: The Role of Vitamin D |
| NCT02596321 | PHASE3 | COMPLETED | A Study Investigating the Immunologic Effects and Safety of 60-day Treatment of the ALK HDM Tablets in Adult Subjects With HDM-Induced Allergic Rhinitis and/or Atopic Asthma |
| NCT02763241 | PHASE3 | COMPLETED | Cleanoze® Irrigation Device With Powder Preparation Versus Conventional Irrigation Method for Chronic Rhinitis |
| NCT02795273 | PHASE2/PHASE3 | WITHDRAWN | Efficacy and Safety of Grass-SPIRE Registration Study |
| NCT03394508 | PHASE2/PHASE3 | COMPLETED | The Safety and Efficacy of Intralymphatic Immunotherapy in Pollen Allergic Adolescents and Young Adults With Asthma |
| NCT00078195 | PHASE2 | COMPLETED | Omalizumab (Xolair) and Allergy Shots For the Treatment of Seasonal Allergies |
| NCT00291642 | PHASE2 | COMPLETED | A Study to Compare the Efficacy of Levocetirizine to Placebo in Reducing Symptoms of Seasonal Allergic Rhinitis (SAR) in Sensitive Subjects Exposed to Ragweed Pollen |
| NCT00857779 | PHASE2 | COMPLETED | Study on Pharmacodynamic Parameter and Tolerability With Subcutaneous Immunotherapy in Grass Pollen Allergic Patients |
| NCT00978029 | PHASE2 | COMPLETED | Safety Study of Ragweed Allergy Immunotherapy Tablet in Subjects 50 Years of Age and Older (Study P06081) |
| NCT01330017 | PHASE2 | COMPLETED | Effects of Phenylephrine on Nasal Congestion in Participants With Seasonal Allergic Rhinitis (P08156 AM2)(Completed) |
| NCT01424397 | PHASE2 | COMPLETED | Intranasal SB-705498 in Allergic Rhinitis (AR) Patients |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| LEVOCETIRIZINE | 4 | 16 |
| MONTELUKAST | 4 | 4 |
| PSEUDOEPHEDRINE | 4 | 4 |
| DESLORATADINE | 4 | 3 |
| FEXOFENADINE | 4 | 3 |
| LORATADINE | 4 | 3 |
| PHENYLEPHRINE | 4 | 3 |
| ALBUTEROL | 4 | 2 |
| MOMETASONE FUROATE | 4 | 2 |
| OLOPATADINE | 4 | 2 |
| XYLOMETAZOLINE | 4 | 2 |
| BETAMETHASONE | 4 | 1 |
| BROMPHENIRAMINE | 4 | 1 |
| BUDESONIDE | 4 | 1 |
| CAPSAICIN | 4 | 1 |
| CETIRIZINE | 4 | 1 |
| DIPHENHYDRAMINE | 4 | 1 |
| FLUTICASONE FUROATE | 4 | 1 |
| FLUTICASONE PROPIONATE | 4 | 1 |
| LANSOPRAZOLE | 4 | 1 |
| NEOMYCIN | 4 | 1 |
| NIACINAMIDE | 4 | 1 |
| OMALIZUMAB | 4 | 1 |
| PYRIDOXINE | 4 | 1 |
| QUININE SULFATE | 4 | 1 |
| RETINOL | 4 | 1 |
| TRIAMCINOLONE ACETONIDE | 4 | 1 |
| COCOA | 3 | 1 |
| DROPROPIZINE | 3 | 1 |
| FLUTICASONE | 3 | 1 |
Related Atlas pages
- Drugs: Levocetirizine, Montelukast, Pseudoephedrine, Desloratadine, Fexofenadine, Loratadine, Phenylephrine, Albuterol, Mometasone Furoate, Olopatadine, Xylometazoline, Betamethasone, Brompheniramine, Budesonide, Capsaicin, Cetirizine, Diphenhydramine, Fluticasone Furoate, Fluticasone Propionate, Lansoprazole, Neomycin, Niacinamide, Omalizumab, Pyridoxine, Quinine, Retinol, Triamcinolone Acetonide, Cocoa, Dropropizine, Fluticasone