Esophageal granular cell tumor
disease diseaseOn this page
Also known as esophageal granular cell myoblastomaesophageal granular cell neoplasmesophagus granular cell tumorgranular cell esophageal tumorgranular cell esophageal tumourgranular cell esophagus myoblastomagranular cell esophagus neoplasmgranular cell esophagus tumorgranular cell myoblastoma of esophagusgranular cell myoblastoma of oesophagusgranular cell myoblastoma of the esophagusgranular cell myoblastoma of the oesophagusgranular cell neoplasm of esophagusgranular cell neoplasm of oesophagusgranular cell neoplasm of the esophagusgranular cell neoplasm of the oesophagusgranular cell oesophagus myoblastomagranular cell oesophagus neoplasmgranular cell oesophagus tumour
Summary
Esophageal granular cell tumor (MONDO:0003251) is a cancer. A subtype of granular cell tumor — 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 | esophageal granular cell tumor |
| Mondo ID | MONDO:0003251 |
| DOID | DOID:5040 |
| ICD-11 | 1070074406 |
| NCIT | C5700 |
| UMLS | C1333448 |
| MedGen | 234228 |
| GARD | 0023422 |
| Anatomy (UBERON) | UBERON:0001043 |
| Is cancer (heuristic) | yes |
Also known as: esophageal granular cell myoblastoma · esophageal granular cell neoplasm · esophageal granular cell tumor · esophagus granular cell tumor · granular cell esophageal tumor · granular cell esophageal tumour · granular cell esophagus myoblastoma · granular cell esophagus neoplasm · granular cell esophagus tumor · granular cell myoblastoma of esophagus · granular cell myoblastoma of oesophagus · granular cell myoblastoma of the esophagus · granular cell myoblastoma of the oesophagus · granular cell neoplasm of esophagus · granular cell neoplasm of oesophagus · granular cell neoplasm of the esophagus · granular cell neoplasm of the oesophagus · granular cell oesophagus myoblastoma · granular cell oesophagus neoplasm · granular cell oesophagus tumour (+6 more)
Disease family
This is a subtype of granular cell tumor. 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 › nervous system disorder › peripheral nervous system disorder › peripheral nervous system neoplasm › nerve sheath neoplasm › granular cell tumor › esophageal granular cell tumor
Related subtypes (8): cutaneous granular cell tumor, breast granular cell tumor, benign granular cell tumor, granular cell cancer, vulvar granular cell tumor, mediastinal granular cell myoblastoma, neurohypophysis granular cell tumor, congenital epulis
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.