multiple endocrine neoplasia type 1

Summary

DOID:10017 - multiple endocrine neoplasia type 1

Disease Ontology 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.

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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: men1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0007540 - multiple endocrine neoplasia type 1

MONDO:0007540 - multiple endocrine neoplasia type 1

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

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

Parent(s): autosomal dominant disease (is_a), multiple endocrine neoplasia (is_a), syndrome (is_a)