Intestinal neuroendocrine tumor G1
MONDO:0021533A 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.
Also known as: carcinoid tumor of intestine, carcinoid tumor of the intestine, carcinoid tumour of intestine, carcinoid tumour of the intestine, grade 1 neuroendocrine neoplasm of intestine, intestinal NET G1, intestinal carcinoid tumor, intestinal carcinoid tumour
1472 clinical trials for this condition and its sub-types, 5 tagged with Intestinal neuroendocrine tumor G1 itself.
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Sub-types of Intestinal neuroendocrine tumor G1
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Small intestinal neuroendocrine tumor G1 3 trials · 5 incl. sub-types
2 sub-types
- Ileal neuroendocrine tumor G1 3 trials
- Jejunal neuroendocrine tumor G1 0 trials
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Colorectal neuroendocrine tumor G1 1 trial · 4 incl. sub-types
2 sub-types
- Colon neuroendocrine tumor G1 1 trial · 3 incl. sub-types Sub-types →
- Rectal neuroendocrine tumor G1 1 trial