Multiple endocrine neoplasia type 1

MONDO:0007540

An autosomal dominant tumor predisposition syndrome caused by pathogenic variants in the MEN1 gene, characterized by an increased risk of tumors of the parathyroid glands, pituitary gland, and foregut neuroendocrine tumors (most commonly pancreatic islet cells).

Also known as: multiple endocrine adenomatosis, MEA type 1, MEA type I, MEN1, MEN1 multiple endocrine neoplasia, MEN1 syndrome, MEN1-related multiple endocrine neoplasia, Wermer syndrome

1597 clinical trials for this condition and its sub-types, 38 tagged with Multiple endocrine neoplasia type 1 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by

Showing the 400 most recently updated of 753 trials in this tab.