Esophageal Granular Cell Tumor

Preferred Label : Esophageal Granular Cell Tumor;

NCIt synonyms : Granular Cell Myoblastoma of the Esophagus; Granular Cell Esophageal Tumor; Granular Cell Esophagus Neoplasm; Granular Cell Esophagus Myoblastoma; Granular Cell Esophagus Tumor; Granular Cell Neoplasm of the Esophagus; Esophageal Granular Cell Neoplasm; Esophageal Granular Cell Myoblastoma; Granular Cell Neoplasm of Esophagus; Granular Cell Myoblastoma of Esophagus; Granular Cell Tumor of the Esophagus; Granular Cell Tumor of Esophagus;

NCIt definition : A tumor that usually presents with small nodules or small sessile polyps, predominantly in the distal esophagus. Histologically, it is composed of sheets of oval to polygonal cells with a small central nucleus and abundant granular cytoplasm. This is usually a benign tumor. (WHO, 2000);

Neoplastic status : Undetermined;

Details

Origin ID

C5700;

UMLS CUI

C1333448;

Automatic exact mappings (from CISMeF team)
- Granular cell tumour of oesophagus [ICD-11 More detail]
- malignant granular cell esophageal tumor [DO Concept]
DO Cross reference
- malignant granular cell esophageal tumor [DO Concept]
Has associated anatomic sites
- Digestive System [NCIt concept]
- Esophagus [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Granular cell neoplasm of esophagus (disorder) [SNOMED CT concept]
- malignant granular cell esophageal tumor [DO Concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Neuroepithelial Cell and Neoplastic Perineural Cell [NCIt concept]
- Neoplastic Perineural Cell [NCIt concept]
- Neoplastic Polygonal Cell with Abundant Granular Cytoplasm [NCIt concept]
disease_has_normal_cell_origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
- Perineural Cell [NCIt concept]
disease_has_normal_tissue_origin
- Nerve Tissue and Nerve Sheaths [NCIt concept]
- Nerve Tissue, Neuroepithelial Tissue, and Nerve Sheaths [NCIt concept]
disease_has_primary_anatomic_site
- Esophagus [NCIt concept]
disease_mapped_to_gene
- ATP6AP1 Gene [NCIt concept]
- ATP6AP2 Gene [NCIt concept]
disease_may_have_molecular_abnormality
- ATP6AP1 Gene Mutation [NCIt concept]
- ATP6AP2 Gene Mutation [NCIt concept]

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