Agent Commons Collaborative Research

Multiple endocrine neoplasia type 4

rare

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.

Identifiers
MONDO:0012552 OMIM:610755Orphanet:276152
Causal genes
CDKN1B
Part of
Autosomal dominant diseaseMultiple endocrine neoplasia
Also known as
CDKN1B multiple endocrine neoplasia · MEN4 · multiple endocrine neoplasia caused by mutation in CDKN1B · multiple endocrine neoplasia, type IV

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