multiple endocrine neoplasia type 2A

MeSH: D018813ORPHA: 247698

Overview

autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis

Available Treatments (0)

No treatments linked yet

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

Classification & Codes

MeSH Code

D018813

Orphanet Code

ORPHA:247698
multiple endocrine neoplasia type 2A
MeSHD018813
OrphanetORPHA:247698
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO