Mesenteric Gastrointestinal Stromal Tumor

Preferred Label : Mesenteric Gastrointestinal Stromal Tumor;

NCIt synonyms : Mesenteric EGIST; Mesenteric Extragastrointestinal Stromal Tumor;

NCIt related terms : Mesenteric Gastrointestinal Stromal Tumor (GIST);

NCIt definition : A gastrointestinal stromal tumor that arises from the mesentery. This is an extragastrointestinal tumor, meaning that it does not arise directly from the gastrointestinal tract.;

Neoplastic status : Undetermined;

Details

Origin ID

C40339;

UMLS CUI

C1513146;

Disease excludes normal cell origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Excludes anatomical site(s)
- Bone [NCIt concept]
- Gastrointestinal Tract [NCIt concept]
Has associated anatomic sites
- Connective and Soft Tissue [NCIt concept]
- Peritoneal Cavity [NCIt concept]
- Peritoneum [NCIt concept]
- Peritoneum and Retroperitoneum [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Stromal Cell [NCIt concept]
disease_has_normal_cell_origin
- Connective and Soft Tissue Cell [NCIt concept]
- Interstitial Cell of Cajal [NCIt concept]
- Stromal Cell [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Peritoneum [NCIt concept]
- Soft Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Abdomen [NCIt concept]
- Mesentery [NCIt concept]
- Peritoneal Cavity [NCIt concept]
- Peritoneum [NCIt concept]
disease_mapped_to_gene
- KIT Gene [NCIt concept]
- PDGFRA Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Loss of Chromosome 14 [NCIt concept]
- Loss of Chromosome 1p [NCIt concept]
- Loss of Chromosome 22 [NCIt concept]
disease_may_have_molecular_abnormality
- KIT Gene Mutation [NCIt concept]
- PDGFRA Gene Mutation [NCIt concept]

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