has material basis in germline mutation in CDKN1B autosomal dominant disease multiple endocrine neoplasia type 4 https://www.malacards.org/card/multiple_endocrine_neoplasia_type_iv icd11.foundation:157945677 SCTID:715907003 GARD:0017275 multiple endocrine neoplasia type 4 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. UMLS:C1970712 multiple endocrine neoplasia, type IV Orphanet:276152 DOID:0080137 MONDO:0012552 multiple endocrine neoplasia caused by mutation in CDKN1B OMIM:610755 MEDGEN:373469 CDKN1B multiple endocrine neoplasia NCIT:C157449 MESH:C567059 MEN4 multiple endocrine neoplasia