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- Be8b23aa26ad3ad9dc54a61da0d9ba64a hasDbXref "Orphanet:652" @default.
- Be8b23aa26ad3ad9dc54a61da0d9ba64a type Axiom @default.
- Be8b23aa26ad3ad9dc54a61da0d9ba64a annotatedProperty IAO_0000115 @default.
- Be8b23aa26ad3ad9dc54a61da0d9ba64a annotatedSource MONDO_0007540 @default.
- Be8b23aa26ad3ad9dc54a61da0d9ba64a 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.