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- B225f3bb80ca13e42fb52a37633e45b7c hasDbXref "Orphanet:652" @default.
- B225f3bb80ca13e42fb52a37633e45b7c type Axiom @default.
- B225f3bb80ca13e42fb52a37633e45b7c annotatedProperty IAO_0000115 @default.
- B225f3bb80ca13e42fb52a37633e45b7c annotatedSource MONDO_0007540 @default.
- B225f3bb80ca13e42fb52a37633e45b7c annotatedTarget "Multiple endocrine neoplasia Type 1 (MEN1) is a frequent form of MEN, a rare inherited cancer syndrome, characterized by the development of neuroendocrine tumors of the parathyroid, pancreas, and anterior pituitary gland, and less commonly the adrenal cortical gland, with other non-endocrine tumors in some patients." @default.