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Disease Ontology Browser
multiple endocrine neoplasia type 1 (DOID:10017)
Synonyms: MEN type I; multiple endocrine neoplasia type 1; Wermer syndrome; Wermer's syndrome
Alt IDs: OMIM:131100, ICD10CM:E31.21, ICD9CM:258.01, MESH:D018761, NCI:C3225, ORDO:652, UMLS_CUI:C0025267
Definition: An autosomal dominant disease 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.

Disease References using Mouse Models (7)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/16/2017
MGI 6.09
The Jackson Laboratory