Acute pharyngitis

disease
On this page

Also known as pharyngitis, acute

Summary

Acute pharyngitis (MONDO:0020600) is a disease with 4 GWAS associations across 17 studies and 8 clinical trials. Top therapeutic interventions include esflurbiprofen, flurbiprofen, and menotropins. A subtype of pharyngitis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • GWAS associations: 4
  • Clinical trials: 8

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameacute pharyngitis
Mondo IDMONDO:0020600
EFOEFO:0009657
ICD-10-CMJ02
ICD-111791890273
NCITC34355
SNOMED CT363746003
UMLSC0001344
MedGen114
Is cancer (heuristic)no

Also known as: acute pharyngitis · pharyngitis, acute

Data availability: 4 GWAS associations (17 studies).

Disease family

This is a subtype of pharyngitis. 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 disorderupper respiratory tract disorderpharyngitisacute pharyngitis

Related subtypes (1): streptococcal sore throat

Genetics & variants

GWAS landscape

4 GWAS associations across 17 studies. Top hits map to 0 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
rs1422291998e-09MIR3144 - RNU6-214P?
chr2:709013833e-08T2.09
chr3:1150561153e-08C0.07
chr7:1542008945e-08C2.76

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90473640UK Biobank Whole-Genome Sequencing Consortium202522,222436,218Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90667848UK Biobank Whole-Genome Sequencing Consortium202522,222436,218Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90478079Verma A202414,147401,754Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90080087Backman JD202110,891351,064Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90084073Backman JD202110,891351,064Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90080086Backman JD20216,744365,218Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90084072Backman JD20216,744365,218Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90478078Verma A20246,152102,654Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90481102Verma A20246,152102,654Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90726940Kim HI20264,82239,204Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding0
Tier 2: splice/UTR0
Tier 3: regulatory0
Tier 4: intronic/intergenic4

MAF distribution

BucketVariants
common (>=0.05)0
low_freq (0.01-0.05)0
rare (<0.01)0
unknown4

Functional consequences

ConsequenceCount
unknown3
intergenic_variant1

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
rs1422291996120245192G>Aintergenic_variantMIR3144 - RNU6-214P8e-09Tier 4: intronic/intergenic
chr2:709013833e-08Tier 4: intronic/intergenic
chr3:1150561153e-08Tier 4: intronic/intergenic
chr7:1542008945e-08Tier 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: 8.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified4
PHASE22
PHASE31
PHASE2/PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01986361PHASE3COMPLETEDPlacebo-Controlled Onset-of-Action Study of Flurbiprofen Utilizing the Double-Stopwatch Method
NCT04027322PHASE2/PHASE3COMPLETEDInhaled Steroids for Acute Pharyngitis.
NCT06932328PHASE2RECRUITINGQinqiao Yan Shu Granules for the Treatment of Acute Pharyngitis (Exterior Wind-Heat Syndrome) Phase II Clinical Trial
NCT04470089PHASE2TERMINATEDA Clinical Trial Investigating the Short-term Relief of Symptoms of Acute Pharyngitis by Treatment With Three Different Doses of MYRAMISTIN™ Oromucosal Spray
NCT07569939Not specifiedNOT_YET_RECRUITINGEvaluation of Treatments for Sore Throat Associated With Acute Pharyngitis and/or Viral Tonsillitis
NCT01720927Not specifiedCOMPLETEDPakistan Epidemiological Survey in Acute Pharyngitis
NCT02160912Not specifiedCOMPLETEDNon Interventional Study (NIS) Regarding the Application of Ectoin Mund- & Rachenspray in Patients With Acute Laryngitis and/or Acute Pharyngitis
NCT04203810Not specifiedCOMPLETEDEffectiveness and Tolerability of Ectoin® Mouth and Throat Spray Althaea Honey (ERS09)

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
ESFLURBIPROFEN41
FLURBIPROFEN41
MENOTROPINS41
SODIUM CHLORIDE41
MIRAMISTIN21