Empty nose syndrome
disease diseaseOn this page
Also known as ENSnasal iatrogenic dysfunctionpost-turbinectomy syndromesecondary atrophic rhinitis
Summary
Empty nose syndrome (MONDO:1060148) is a disease and 3 clinical trials. Top therapeutic interventions include botulinum toxin type a. A subtype of atrophic rhinitis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 3
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | empty nose syndrome |
| Mondo ID | MONDO:1060148 |
| UMLS | C3888849 |
| MedGen | 1876481 |
| GARD | 0028165 |
| Is cancer (heuristic) | no |
Also known as: ENS · nasal iatrogenic dysfunction · post-turbinectomy syndrome · secondary atrophic rhinitis
Disease family
This is a subtype of atrophic rhinitis. 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 › otorhinolaryngologic disease › nasal disorder › nasal cavity disorder › rhinitis › atrophic rhinitis › empty nose syndrome
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: 3.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 2 |
| PHASE1/PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00732680 | PHASE1/PHASE2 | TERMINATED | Benefits of the Use of Botox in the Treatment of Empty Nose Syndrome Syndrome |
| NCT07215013 | Not specified | NOT_YET_RECRUITING | Acoustic Resonance Therapy for Treating Empty Nose Syndrome |
| NCT02230423 | Not specified | COMPLETED | Trigeminal Endonasal Perception: A Predictor for Septoplasty Outcome |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| BOTULINUM TOXIN TYPE A | 4 | 1 |
Related Atlas pages
- Drugs: Botulinum Toxin Type A