Cecum neuroendocrine tumor G1

MONDO:0006126

A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the cecum. 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: caecal carcinoid tumor, caecal carcinoid tumour, caecum NET G1, caecum carcinoid tumor, caecum carcinoid tumor (disease), caecum carcinoid tumour, caecum carcinoid tumour (disease), caecum neuroendocrine neoplasm G1

1494 clinical trials for this condition and its sub-types, 3 tagged with Cecum neuroendocrine tumor G1 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Sub-types of Cecum neuroendocrine tumor G1

Sort by