Colorectal neuroendocrine tumor G1
MONDO:0006162A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the colon or rectum. 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: colorectal NET G1, colorectal carcinoid tumor, colorectal carcinoid tumour, colorectal neuroendocrine tumor G1, colorectum NET G1, colorectum carcinoid tumor, colorectum carcinoid tumour, colorectum neuroendocrine neoplasm G1
1489 clinical trials for this condition and its sub-types, 1 tagged with Colorectal neuroendocrine tumor G1 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Colorectal neuroendocrine tumor G1
-
Colon neuroendocrine tumor G1 1 trial · 3 incl. sub-types
4 sub-types
- Cecum neuroendocrine tumor G1 3 trials Sub-types →
- Ileal neuroendocrine tumor G1 3 trials
- Ascending colon neuroendocrine tumor G1 0 trials
- Jejunal neuroendocrine tumor G1 0 trials
-
Rectal neuroendocrine tumor G1 1 trial