Visualize
Metadata
DOID DOID:10016
Name multiple endocrine neoplasia type 2B
Definition An autosomal dominant disease characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities.
http://en.wikipedia.org/wiki/Multiple_endocrine_neoplasia_type_2b, http://ghr.nlm.nih.gov/condition/multiple-endocrine-neoplasia, http://www.merckmanuals.com/professional/endocrine_and_metabolic_disorders/multiple_endocrine_neoplasia_men_syndromes/multiple_endocrine_neoplasia_type_2b_men_2b.html, https://www.ncbi.nlm.nih.gov/pubmed/15965261, https://www.rarediseases.org/rare-disease-information/rare-diseases/byID/1244/viewAbstract
Xrefs

CSP2005:2009-6300

ICD10CM:E31.23

ICD9CM:258.03

MESH:D018814

NCI2004_11_17:C3227

NCI:C3227

OMIM:162300

ORDO:247709

SNOMEDCT_US_2018_03_01:61530001

UMLS_CUI:C0025269

Subsets

DO_FlyBase_slim

DO_rare_slim

NCIthesaurus

Synonyms

MEN type IIB [EXACT]

MEN2B [EXACT]

mucosal neuroma syndrome [EXACT]

multiple endocrine neoplasia type 2b [EXACT]

Multiple endocrine neoplasia, type 3 [EXACT]

Wagenmann-Froboese syndrome [EXACT]

Relationships

is_a autosomal dominant disease

Add an item to the term tracker