|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 1 from the curated CTD Gene-Disease Associations dataset.
|MEN1||multiple endocrine neoplasia I||2.88009|