Summary Literature (0)

DOID:10017 - multiple endocrine neoplasia type 1

Disease Ontology 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.

Synonyms: MEN type I, Wermer syndrome, Wermer's syndrome, multiple endocrine neoplasia type 1,

Echinobase Genes :


OMIM:

MIM:131100 - multiple endocrine neoplasia, type i; men1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee