multiple endocrine neoplasia type 2B

MeSH: D018814ORPHA: 247709

Overview

autosomal dominant disease characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

D018814

Orphanet Code

ORPHA:247709
multiple endocrine neoplasia type 2B
MeSHD018814
OrphanetORPHA:247709
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO