Multiple endocrine neoplasia, type 1 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/131100
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Genes

1 genes associated with the Multiple endocrine neoplasia, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
MEN1 multiple endocrine neoplasia I