About   Help   FAQ
Disease Ontology Browser
multiple endocrine neoplasia type 1 (DOID:10017)
Alliance: disease page
Synonyms: MEN type I; 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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.14
The Jackson Laboratory