Chronic laryngitis
disease diseaseOn this page
Also known as laryngitis, chronic
Summary
Chronic laryngitis (MONDO:0001369) is a disease with 6 GWAS associations across 4 studies and 2 clinical trials. Top therapeutic interventions include esomeprazole. A subtype of laryngitis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- GWAS associations: 6
- Clinical trials: 2
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | chronic laryngitis |
| Mondo ID | MONDO:0001369 |
| DOID | DOID:11797 |
| ICD-10-CM | J37.0 |
| ICD-11 | 2009723608 |
| NCIT | C26975 |
| SNOMED CT | 29951006 |
| UMLS | C0155836 |
| MedGen | 102342 |
| Is cancer (heuristic) | no |
Also known as: laryngitis, chronic
Data availability: 6 GWAS associations (4 studies).
Disease family
This is a subtype of laryngitis. 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 › upper respiratory tract disorder › laryngeal disorder › laryngitis › chronic laryngitis
Related subtypes (3): laryngotracheitis, acute laryngitis, laryngeal tuberculosis
Genetics & variants
GWAS landscape
6 GWAS associations across 4 studies. Top hits map to 4 distinct genes (as reported by GWAS).
Top associations by p-value
| rsID | p-value | Gene | Risk allele | Odds ratio |
|---|---|---|---|---|
| rs565266096 | 1e-14 | RORB | G | 3.43 |
| rs187967316 | 7e-14 | NDST4 | T | 4.4 |
| rs184756987 | 8e-13 | SS18 | C | 2.18 |
| rs572966339 | 4e-12 | LINC02466 | C | 4.09 |
| rs144067010 | 1e-11 | CBX1P3 - LINC00303 | T | 3.75 |
| rs796920051 | 4e-11 | SPATC1L - LSS | C | 4.45 |
Top studies (by case count)
| Study | Lead author | Year | Cases | Controls | Title |
|---|---|---|---|---|---|
| GCST90478090 | Verma A | 2024 | 903 | 447,899 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90480234 | Verma A | 2024 | 247 | 121,015 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90482063 | Verma A | 2024 | 247 | 121,015 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90436198 | Zhou W | 2018 | 104 | 390,045 | 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 | 0 |
| Tier 2: splice/UTR | 0 |
| Tier 3: regulatory | 0 |
| Tier 4: intronic/intergenic | 6 |
MAF distribution
| Bucket | Variants |
|---|---|
| common (>=0.05) | 0 |
| low_freq (0.01-0.05) | 0 |
| rare (<0.01) | 6 |
| unknown | 0 |
Functional consequences
| Consequence | Count |
|---|---|
| intron_variant | 4 |
| intergenic_variant | 1 |
| non_coding_transcript_exon_variant | 1 |
Top variants
| rsID | Chr | Pos | Alleles | MAF | Consequence | Gene | p-value | Tier |
|---|---|---|---|---|---|---|---|---|
| rs565266096 | 9 | 74630433 | G>A,T | 0 | intron_variant | RORB | 1e-14 | Tier 4: intronic/intergenic |
| rs187967316 | 4 | 114913365 | T>C | 0.001 | intron_variant | NDST4 | 7e-14 | Tier 4: intronic/intergenic |
| rs184756987 | 18 | 26084052 | C>A,G | 0.001 | intron_variant | SS18 | 8e-13 | Tier 4: intronic/intergenic |
| rs572966339 | 4 | 129677938 | C>T | 0 | intron_variant | LINC02466 | 4e-12 | Tier 4: intronic/intergenic |
| rs144067010 | 1 | 203978674 | T>A,C,G | 0 | intergenic_variant | CBX1P3 - LINC00303 | 1e-11 | Tier 4: intronic/intergenic |
| rs796920051 | 21 | 46185113 | C>T | 0 | non_coding_transcript_exon_variant | SPATC1L - LSS | 4e-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
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 2.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01389401 | Not specified | COMPLETED | Salivary Epidermal Growth Factor (EGF) Concentration Before and After Treatment of Reflux Laryngitis |
| NCT01806220 | Not specified | COMPLETED | Laryngeal and Esophageal EGF-r Expression in Patients With Reflux Laryngitis |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| ESOMEPRAZOLE | 4 | 1 |
Related Atlas pages
- Drugs: Esomeprazole