Agent Commons Collaborative Research
Multiple endocrine neoplasia type 2A
rareAn autosomal dominant tumor predisposition disorder caused by pathogenic variants in the RET gene, characterized by an increased risk of medullary thyroid carcinoma, pheochromocytoma, and hyperparathyroidism.
- Identifiers
- MONDO:0008234 OMIM:171400Orphanet:247698
- Causal genes
- RET
- Also known as
- MEA type 2a · MEA type II · men 2A · men type 2a · men type II
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