JSON

intestinal neuroendocrine tumor G1

^ http://purl.obolibrary.org/obo/MONDO_0021533

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 ]

Term info

database cross reference
  • UMLS:C0349535 (OMIM:114900)
  • NCIT:C4637 (MONDO:equivalentTo)
  • SCTID:276816003 (MONDO:equivalentTo)
  • MESH:C562842 (MONDO:equivalentTo)
  • OMIM:114900 (MONDO:equivalentTo)
IAO 0000233

https://github.com/monarch-initiative/mondo/issues/4207

definition

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.

exactMatch

http://identifiers.org/snomedct/276816003, http://linkedlifedata.com/resource/umls/id/C0349535, http://purl.obolibrary.org/obo/NCIT_C4637, http://identifiers.org/mesh/C562842, https://omim.org/entry/114900

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0003847

has exact synonym

carcinoid tumor of the intestine, intestine neuroendocrine neoplasm G1, intestine carcinoid tumor, intestine carcinoid tumor (disease), intestinal NET G1, intestine NET G1, intestinal carcinoid tumor, carcinoid tumor of intestine, intestine neuroendocrine tumor, well differentiated, low grade, intestinal neuroendocrine tumor G1, grade 1 neuroendocrine neoplasm of intestine

id

MONDO:0021533