Also Known As
MEN2BRET-related multiple endocrine neoplasia type 2BWagenmann-Froboese syndromemen 2Bmen IIBmen type 2Bmen type IIBmucosal neuroma syndromemultiple endocrine adenomatosis type IIBmultiple endocrine neoplasia IIBmultiple endocrine neoplasia type 2Bmultiple endocrine neoplasia type 3multiple endocrine neoplasia type IIBmultiple endocrine neoplasia type IIImultiple endocrine neoplasia, type 3multiple endocrine neoplasia, type IIINeuromata, mucosal, with endocrine tumorsNeuromata, mucosal, with endocrine tumoursmucosal Neuroma syndromemultiple endocrine neoplasia, type 2Bmultiple endocrine neoplasia, type 3 (formerly)multiple endocrine neoplasia, type IIBmultiple endocrine neoplasia, type III, formerly
Definition
An autosomal dominant disorder caused by specific pathogenic variants in the RET gene, characterized by an increased risk of very early onset medullary thyroid carcinoma, pheochromocytoma, and hyperparathyroidism, and mucosal neuromas.