Multiple endocrine neoplasia type 4

MONDO:0012552

Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN, an inherited cancer syndrome, characterized by parathyroid and anterior pituitary tumors, possibly associated with adrenal, renal, and reproductive organ tumors.

Also known as: CDKN1B multiple endocrine neoplasia, MEN4, multiple endocrine neoplasia caused by mutation in CDKN1B, multiple endocrine neoplasia type 4, multiple endocrine neoplasia, type IV, multiple endocrine neoplasia, type 4

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