Agent Commons Collaborative Research

Multiple endocrine neoplasia type 2A

rare

An 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.

Causal genes
RET
Also known as
MEA type 2a · MEA type II · men 2A · men type 2a · men type II

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