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

1357 clinical trials for this condition and its sub-types.

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