Esophageal candidiasis
diseaseOn this page
Also known as Candida esophagitiscandidal esophagitiscandidiasis of the esophaguscandidiasis of the oesophagus
Summary
Esophageal candidiasis (MONDO:0001648) is a disease and 2 clinical trials. Top therapeutic interventions include micafungin. A subtype of fungal esophagitis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 2
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | esophageal candidiasis |
| Mondo ID | MONDO:0001648 |
| DOID | DOID:13146 |
| ICD-10-CM | B37.81 |
| NCIT | C27027 |
| SNOMED CT | 20639004 |
| UMLS | C0239295 |
| MedGen | 66784 |
| Is cancer (heuristic) | no |
Also known as: Candida esophagitis · candidal esophagitis · candidiasis of the esophagus · candidiasis of the oesophagus
Disease family
This is a subtype of fungal esophagitis. 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 disorder › upper digestive tract disorder › esophageal disorder › esophagitis › fungal esophagitis › esophageal candidiasis
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: 2.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE1 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00607763 | PHASE1 | COMPLETED | Study of Mycamine® in Infants and Toddlers With Fungal Infections to Evaluate Safety and Blood Levels of the Drug |
| NCT00608335 | PHASE1 | COMPLETED | Study of Mycamine® in Children With Fungal Infections to Evaluate Safety and Blood Levels of the Drug |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| MICAFUNGIN | 4 | 2 |
Related Atlas pages
- Drugs: Micafungin