A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the small or large 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:C4637 ]
Synonyms: carcinoid tumor of the intestine intestine neuroendocrine neoplasm G1 intestine carcinoid tumor intestine carcinoid tumour (disease) intestine carcinoid tumour intestinal carcinoid tumor intestine NET G1 carcinoid tumor of intestine intestine neuroendocrine tumor, well differentiated, low grade carcinoid tumour of the intestine intestine carcinoid tumor (disease) intestinal NET G1 carcinoid tumour of intestine intestinal carcinoid tumour intestinal neuroendocrine tumor G1 grade 1 neuroendocrine neoplasm of intestine
Term information
- MESH:C562842 (MONDO:equivalentTo)
- SCTID:276816003 (MONDO:equivalentTo)
- UMLS:C0349535 (MONDO:equivalentTo)
- MEDGEN:138099 (MONDO:equivalentTo)
- NCIT:C4637 (MONDO:equivalentTo)
- OMIM:114900 (MONDO:equivalentTo)
gard_rare, otar, rare
http://identifiers.org/snomedct/276816003
http://linkedlifedata.com/resource/umls/id/C0349535
http://identifiers.org/medgen/138099
http://purl.obolibrary.org/obo/NCIT_C4637
http://identifiers.org/mesh/C562842
https://omim.org/entry/114900
Term relations
- neuroendocrine neoplasm and has characteristic some tumor grade 1, general grading system and disease has location some intestine