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DOID:10016 - multiple endocrine neoplasia type 2B
Disease Ontology Definition: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.
Synonyms: MEN type IIB, MEN2B, Multiple endocrine neoplasia, type 3, Wagenmann-Froboese syndrome, mucosal neuroma syndrome, multiple endocrine neoplasia type 2b,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:162300 - multiple endocrine neoplasia, type iib; men2b |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a)