multiple endocrine neoplasia type 2 Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Multiple endocrine neoplasia type 2 (MEN2) is a polyglandular cancer syndrome characterized by the occurrence of medullary thyroid carcinoma (MTC), pheochromocytoma (PCC; see these terms) and, in one variant, primary hyperparathyroidism (PHPT). (Orphanet Rare Disease Ontology, Orphanet_653)
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1 genes associated with the disease multiple endocrine neoplasia type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
RET ret proto-oncogene