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
D018813Orphanet Code
ORPHA:247698multiple endocrine neoplasia type 2A
| MeSH | D018813 |
| Orphanet | ORPHA:247698 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO