Multiple Endocrine Neoplasia Type 1 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description 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. (Human Disease Ontology, DOID_10017)
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1 genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 1 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MEN1 multiple endocrine neoplasia I 2.88009