DO_rare_slim DO_FlyBase_slim NCIthesaurus has material basis in autosomal dominant disease multiple endocrine neoplasia type 2B disease_ontology MESH:D018814 A multiple endocrine neoplasia characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities. ICD10CM:E31.23 UMLS_CUI:C0025269 MIM:162300 NCI:C3227 SNOMEDCT_US_2025_09_01:61530001 DOID:10016 ICD9CM:258.03 MEN type IIB MEN2B Multiple endocrine neoplasia, type 3 OMIM mapping confirmed by DO. [SN]. ORDO:247709 Wagenmann-Froboese syndrome mucosal neuroma syndrome multiple endocrine neoplasia autosomal dominant inheritance