Reactive airway disease
diseaseOn this page
Also known as hyperactive airway diseasereactive airway disease (AQ)
Summary
Reactive airway disease (MONDO:0100470) is a disease and 10 clinical trials. Top therapeutic interventions include betamethasone, dexamethasone, and mannitol. A subtype of respiratory system disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 10
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | reactive airway disease |
| Mondo ID | MONDO:0100470 |
| NCIT | C113673 |
| SNOMED CT | 991000119106 |
| UMLS | C3714497 |
| MedGen | 811342 |
| Is cancer (heuristic) | no |
Also known as: hyperactive airway disease · reactive airway disease (AQ)
Disease family
This is a subtype of respiratory system disorder. 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 › respiratory system disorder › reactive airway disease
Related subtypes (58): lower respiratory tract disorder, respiratory system cancer, respiratory system benign neoplasm, allergic respiratory disease, paranasal sinus disorder, upper respiratory tract disorder, pertussis, severe acute respiratory syndrome, sleep apnea syndrome, diaphragm disorder, pulmonary tuberculosis, altitude sickness, perinatal asphyxia, pulmonary nodular lymphoid hyperplasia, tracheobronchopathia osteochondroplastica, Williams-Campbell syndrome, cystic fibrosis, growth delay-hydrocephaly-lung hypoplasia syndrome, laryngo-onycho-cutaneous syndrome, congenital pulmonary lymphangiectasia, familial primary pulmonary hypoplasia, Mounier-Kuhn syndrome, Young syndrome, lung agenesis-heart defect-thumb anomalies syndrome, sudden infant death-dysgenesis of the testes syndrome, alpha 1-antitrypsin deficiency, hereditary sclerosing poikiloderma with tendon and pulmonary involvement, autoimmune interstitial lung disease-arthritis syndrome, mucopolysaccharidosis-plus syndrome, congenital bronchobiliary fistula, bronchogenic cyst, primary ciliary dyskinesia, congenital pulmonary airway malformation, transient hyperammonemia of the newborn, congenital pulmonary sequestration, Siegler-Brewer-Carey syndrome, tracheal agenesis, 16q24.1 microdeletion syndrome, staphylococcal necrotizing pneumonia, pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis, plastic bronchitis, recurrent respiratory papillomatosis, IgG4-related mediastinitis, bronchopulmonary dysplasia, infantile apnea, diffuse alveolar hemorrhage, respiratory or thoracic malformation, pulmonary agenesis, eosinophilic granuloma, disorder of pharynx, respiratory tract neoplasm, pulmonary alveolar proteinosis with hypogammaglobulinemia, respiratory tract infectious disorder, Middle East respiratory syndrome, acinar dysplasia, pulmonary hypoplasia, isolated left bronchial isomerism, bronchiectasis and nasal polyposis
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
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
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 10.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 7 |
| PHASE4 | 1 |
| EARLY_PHASE1 | 1 |
| PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01241006 | PHASE4 | COMPLETED | Single Oral Dose of Dexamethasone Versus Five Days of Prednisone in Adult Asthma |
| NCT03421730 | PHASE1 | COMPLETED | A Study of the Pharmacokinetics, Safety and Tolerability of Single Doses of VR647 Inhalation Suspension Administered Using the VR647 Inhalation System in Children With Wheezing, Reactive Airway Disease or Mild Asthma |
| NCT02306473 | EARLY_PHASE1 | COMPLETED | The Leaky Lung Test |
| NCT00942201 | Not specified | COMPLETED | Comparison of Oral Dexamethasone Doses in Asthma Exacerbation |
| NCT01625364 | Not specified | COMPLETED | Comparison of Asthma Programs for Schools |
| NCT02973282 | Not specified | COMPLETED | Diagnosing Respiratory Disease in Children Using Cough Sounds |
| NCT03062709 | Not specified | COMPLETED | A Study of Tobacco Smoke and Children With Respiratory Illnesses |
| NCT03131323 | Not specified | UNKNOWN | Nasal Findings in Reactive Airway Diseases |
| NCT03392363 | Not specified | COMPLETED | Diagnosing Respiratory Disease in Children Using Cough Sounds 2 |
| NCT06156436 | Not specified | COMPLETED | A Study Evaluating the Use of ResAppDx v2.0 as an Aid to Diagnose Respiratory Disease in Paediatric Patients in an Emergency Department |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| BETAMETHASONE | 4 | 1 |
| DEXAMETHASONE | 4 | 1 |
| MANNITOL | 4 | 1 |
| PREDNISONE | 4 | 1 |
| SORBITOL | 4 | 1 |
| CHEMBL15720 | 0 | 1 |
Related Atlas pages
- Drugs: Betamethasone, Dexamethasone, Mannitol, Prednisone, Sorbitol