small intestinal neuroendocrine tumor G1
http://purl.obolibrary.org/obo/MONDO_0000540
A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the small intestine. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent. [ NCIT:C4638 ]
Term info
- UMLS:C0349536 (NCIT:C4638)
- NCIT:C4638 (MONDO:equivalentTo)
- SCTID:276818002 (MONDO:equivalentTo)
- DOID:0050925 (MONDO:equivalentTo)
A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the small intestine. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent.
http://linkedlifedata.com/resource/umls/id/C0349536, http://purl.obolibrary.org/obo/NCIT_C4638, http://purl.obolibrary.org/obo/DOID_0050925, http://identifiers.org/snomedct/276818002
carcinoid tumor of the small bowel, small intestinal neuroendocrine tumor G1, small intestinal NET G1, small intestine neuroendocrine neoplasm G1, small intestine NET G1, small intestine carcinoid tumor, small intestinal carcinoid tumor, carcinoid tumor of the small intestine, grade 1 neuroendocrine neoplasm of small intestine, carcinoid tumor of small intestine, carcinoid tumor of small bowel, small intestine carcinoid tumor (disease), small intestine neuroendocrine tumor, well differentiated, low grade, small bowel carcinoid tumor
small intestine carcinoid neuroendocrine tumor
MONDO:0000540