Benign neoplasm of esophagus
diseaseOn this page
Also known as benign esophageal neoplasmbenign esophageal tumorbenign esophageal tumourbenign esophagus neoplasmbenign esophagus tumorbenign neoplasm of the esophagusbenign neoplasm of the oesophagusbenign oesophagus neoplasmbenign oesophagus tumourbenign tumor of esophagusbenign tumor of the esophagusbenign tumour of oesophagusbenign tumour of the oesophagusesophagus benign neoplasmoesophagus benign neoplasm
Summary
Benign neoplasm of esophagus (MONDO:0021459) is a cancer. A subtype of benign digestive system neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | benign neoplasm of esophagus |
| Mondo ID | MONDO:0021459 |
| ICD-10-CM | D13.0 |
| ICD-11 | 1827459816 |
| NCIT | C3598 |
| SNOMED CT | 92091003 |
| UMLS | C0153942 |
| MedGen | 102297 |
| Anatomy (UBERON) | UBERON:0001043 |
| Is cancer (heuristic) | yes |
Also known as: benign esophageal neoplasm · benign esophageal tumor · benign esophageal tumour · benign esophagus neoplasm · benign esophagus tumor · benign neoplasm of the esophagus · benign neoplasm of the oesophagus · benign oesophagus neoplasm · benign oesophagus tumour · benign tumor of esophagus · benign tumor of the esophagus · benign tumour of oesophagus · benign tumour of the oesophagus · esophagus benign neoplasm · oesophagus benign neoplasm
Disease family
This is a subtype of benign digestive system neoplasm. 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 › benign digestive system neoplasm › benign neoplasm of esophagus
Related subtypes (9): intestinal benign neoplasm, bile duct papillary neoplasm, pleomorphic adenoma, hepatocellular adenoma, benign neoplasm of stomach, benign neoplasm of pancreas, benign neoplasm of oropharynx, benign neoplasm of gallbladder, hepatobiliary benign neoplasm
Subtypes (3): esophageal lipoma, esophagus squamous cell papilloma, esophagus leiomyoma
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: 0.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.