Eosinophilic colitis

disease
On this page

Summary

Eosinophilic colitis (MONDO:0018439) is a disease and 7 clinical trials. A subtype of microscopic colitis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Prevalence: <1 / 1 000 000 (Worldwide) [Orphanet-validated]
  • Clinical trials: 7

Clinical features

Epidemiology

Prevalence records

2 prevalence record(s), Orphanet:

TypeClassValueGeographyValidation
Cases/families196WorldwideValidated
Point prevalence<1 / 1 000 000WorldwideValidated

Identifiers

Disease identifiers

FieldValue
Canonical nameeosinophilic colitis
Mondo IDMONDO:0018439
Orphanet402035
ICD-10-CMK52.82
ICD-111169803773
NCITC27053
SNOMED CT29120000
UMLSC0267448
MedGen75633
GARD0021715
Is cancer (heuristic)no

Disease family

This is a subtype of microscopic colitis. 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 › digestive system disorderintestinal disordergastroenteritiscolitismicroscopic colitiseosinophilic colitis

Related subtypes (2): collagenous colitis, lymphocytic colitis

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: 7.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified7

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02523118Not specifiedRECRUITINGOMEGA: Outcome Measures in Eosinophilic Gastrointestinal Disorders Across the Ages
NCT05199532Not specifiedRECRUITINGEosinophilic Gastrointestinal Disorders Registry
NCT05219903Not specifiedRECRUITINGNational, Multicenter, Retrospective, Prospective Study to Evaluate Pediatric Gastrointestinal Eosinophilic Disorders
NCT00267475Not specifiedCOMPLETEDData Bank for Eosinophilic Disorders
NCT01779154Not specifiedWITHDRAWNEosinophilic Gastrointestinal Disorders Patient Registry
NCT02897271Not specifiedCOMPLETEDCharacteristics of Eosinophilic Gastritis, Enteritis, and Colitis in a Multi-Site Cohort
NCT05719727Not specifiedUNKNOWNPrimary Eosinophilic Colitis in Symptomatic Patients.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.