gastric neuroendocrine tumor G1
http://purl.obolibrary.org/obo/MONDO_0006227
A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the stomach. The vast majority of cases arise from the corpus-fundus region. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent. It may be associated with autoimmune chronic atrophic gastritis, multiple endocrine neoplasia type 1, or it may be sporadic. [ NCIT:P378 ]
Term info
- EFO:1000275 (MONDO:equivalentTo)
- NCIT:C4635 (MONDO:equivalentTo)
- UMLS:C0349529 (NCIT:C4635)
A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the stomach. The vast majority of cases arise from the corpus-fundus region. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent. It may be associated with autoimmune chronic atrophic gastritis, multiple endocrine neoplasia type 1, or it may be sporadic.
http://purl.obolibrary.org/obo/NCIT_C4635, http://linkedlifedata.com/resource/umls/id/C0349529
gastric NET G1, stomach carcinoid tumor, stomach NET G1, grade 1 neuroendocrine neoplasm of stomach, gastric ECL-cell carcinoid tumor, gastric enterochromaffin-like cell neuroendocrine tumor, stomach neuroendocrine tumor, well differentiated, low grade, gastric carcinoid tumor, stomach neuroendocrine neoplasm G1, gastric ECL cell NET, gastric ECL cell, histamine-producing NET, gastric enterochromaffin-like cell carcinoid tumor, gastric ECL cell NET G1
MONDO:0006227