This report describes general characteristics of the group of diseases classified as multiple endocrine neoplasias (MEN). MEN is a genetically heterogeneous disorder, with several causative genes and mapped loci. A listing of MEN subtypes, as defined by OMIM, may be found in the table below, with links to more detailed reports for subtypes that have been investigated using fly models.
[updated Feb. 2015 by FlyBase; FBrf0222196]
For additional information on classification and genetics see http://www.thyroidcancer.com/thyroid-cancer/medullary/genetics.
Multiple endocrine neoplasias are characterized by varying combinations of tumors derived from endocrine glands, including parathyroid, thyroid, pituitary, and adrenal glands. Frequently the tumors are nonmetastasizing, but can cause serious clinical effects due to the inappropriate secretion of endocrine substances. [from MIM:131100, MIM:171400, MIM:162300; 2014.07.03]