has material basis in germline mutation in MEN1 autosomal dominant disease multiple endocrine neoplasia type 1 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/9097 https://github.com/monarch-initiative/mondo/issues/9178 https://rarediseases.info.nih.gov/diseases/3829/multiple-endocrine-neoplasia-type-1 https://www.malacards.org/card/multiple_endocrine_neoplasia_type_i multiple endocrine adenomatosis, type I Wermer's syndrome SCTID:30664006 OMIM:131100 MEN1 ICD9:258.01 multiple endocrine neoplasia type 1 syndrome multiple endocrine neoplasia, type I multiple endocrine adenomatosis UMLS:C0025267 MEDGEN:9957 MEA type 1 men type 1 NORD:1466 MESH:D018761 men type I multiple endocrine neoplasia caused by mutation in MEN1 MedDRA:10028190 ICD10CM:E31.21 MONDO:0007540 An autosomal dominant tumor predisposition syndrome caused by pathogenic variants in the MEN1 gene, characterized by an increased risk of tumors of the parathyroid glands, pituitary gland, and foregut neuroendocrine tumors (most commonly pancreatic islet cells). MEN1 multiple endocrine neoplasia DOID:10017 men 1 MEA type I multiple endocrine neoplasia type 1 multiple endocrine adenomatosis type 1 GARD:0003829 endocrine adenomatosis multiple Orphanet:652 icd11.foundation:1638765741 MEN1 syndrome multiple endocrine neoplasia type I NANDO:2200405 NCIT:C3225 multiple endocrine neoplasia 1 ICD9:237.4 Wermer syndrome MEN1-related multiple endocrine neoplasia multiple endocrine adenomatosis type I familial primary hyperparathyroidism multiple endocrine neoplasia adrenal gland neoplasm