Disease-gene associations mined from literature

Human genes for multiple endocrine neoplasia type 1

Multiple endocrine neoplasia type 1 [DOID:10017]

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:  multiple endocrine neoplasia type 1,  DOID:10017,  MEN type I,  Wermer syndrome,  Wermer's syndrome ...

Linkouts:  OMIM