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
D018814Orphanet Code
ORPHA:247709multiple endocrine neoplasia type 2B
| MeSH | D018814 |
| Orphanet | ORPHA:247709 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO