Hordeolum

disease
On this page

Also known as blepharitis of eyelid glandeyelid gland blepharitisStye

Summary

Hordeolum (MONDO:0005800) is a disease with 11 GWAS associations across 5 studies and 2 clinical trials. Top therapeutic interventions include loteprednol etabonate, neomycin, and framycetin. A subtype of blepharitis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • GWAS associations: 11
  • Clinical trials: 2

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namehordeolum
Mondo IDMONDO:0005800
MeSHD006726
DOIDDOID:9909
ICD-111259721857
NCITC118722
SNOMED CT397513003
UMLSC0019917
MedGen6884
Anatomy (UBERON)UBERON:0013229
Is cancer (heuristic)no

Also known as: blepharitis of eyelid gland · eyelid gland blepharitis · Stye

Data availability: 11 GWAS associations (5 studies).

Disease family

This is a subtype of blepharitis. 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 › disorder of orbital regioneye adnexa disordereyelid disorderblepharitishordeolum

Related subtypes (5): parasitic eyelid infestation, squamous blepharitis, noninfectious dermatoses of eyelid, blepharoconjunctivitis, ulcerative blepharitis

Subtypes (2): hordeolum externum, internal hordeolum

Genetics & variants

GWAS landscape

11 GWAS associations across 5 studies. Top hits map to 0 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
chr6:324402352e-13A0.11
chr19:184791335e-10T0.16
chr5:1322278085e-09G0.08
chr22:439343161e-08T0.1
chr1:229674792e-08T0.1
chr11:14541583e-08GGGGGGGCTTACCTGT0.27
chr8:127885784e-08G0.08
chr15:876327574e-08A2.74
chr19:158726754e-08A0.08
chr3:662898624e-08G2.79
chr13:323182315e-08A3.37

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90473375UK Biobank Whole-Genome Sequencing Consortium202511,696446,744Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90667808UK Biobank Whole-Genome Sequencing Consortium202511,696446,744Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90079863Backman JD20214,139377,132Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90083849Backman JD20214,139377,132Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90473376UK Biobank Whole-Genome Sequencing Consortium20253909,223Whole-genome sequencing of 490,640 UK Biobank participants.

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/intergenic11

MAF distribution

BucketVariants
common (>=0.05)0
low_freq (0.01-0.05)0
rare (<0.01)0
unknown11

Functional consequences

ConsequenceCount
unknown11

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
chr6:324402352e-13Tier 4: intronic/intergenic
chr19:184791335e-10Tier 4: intronic/intergenic
chr5:1322278085e-09Tier 4: intronic/intergenic
chr22:439343161e-08Tier 4: intronic/intergenic
chr1:229674792e-08Tier 4: intronic/intergenic
chr11:14541583e-08Tier 4: intronic/intergenic
chr8:127885784e-08Tier 4: intronic/intergenic
chr15:876327574e-08Tier 4: intronic/intergenic
chr19:158726754e-08Tier 4: intronic/intergenic
chr3:662898624e-08Tier 4: intronic/intergenic
chr13:323182315e-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

Drugs indicated for this disease

0 approved, 1 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.

DrugDevelopment status
GramicidinPhase 3 (in late-stage trials)

Clinical trials & evidence

Clinical trials

Clinical trials: 2.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE41
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00420628PHASE4COMPLETEDPediatric Zylet Safety and Efficacy Study
NCT00534391PHASE3UNKNOWNComparison of Combination Antibiotics Eyedrop to Artificial Tear in Hordeolum After Incision and Curettage

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
LOTEPREDNOL ETABONATE41
NEOMYCIN41
FRAMYCETIN31
CHEMBL375409301
CHEMBL429924701
VEHICLE01