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| Term | multiple endocrine neoplasia type 1 | ID (Ontology) | DOID:10017 (Human Disease) | |||||||||||||||||||||||
| Definition | A multiple endocrine neoplasia that has_material_basis_in a mutation in the MEN1 tumor suppressor gene and is characterized by over active endocrine glands frequently involving tumors of the parathyroid glands, the pituitary gland, and the pancreas. | |||||||||||||||||||||||||
| Also Known As | "MEN type I" ; "Wermer syndrome" ; "Wermer's syndrome" | |||||||||||||||||||||||||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease____ syndrome | |__multiple endocrine neoplasia__| multiple endocrine neoplasia type 1 9 rec. |
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autosomal dominant disease multiple endocrine neoplasia |
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External Crossreferences & Linkouts
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GARD:3829 ICD10CM:E31.21 ICD9CM:258.01 MESH:D018761 MIM:131100 NCI:C3225 ORDO:652 SNOMEDCT_US_2023_03_01:30664006 UMLS_CUI:C0025267 |
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