Multiple endocrine neoplasia type 2A

MONDO:0008234

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.

Also known as: MEA type 2a, MEA type II, MEN2A, RET-related multiple endocrine neoplasia type 2A, Sipple syndrome, men 2A, men type 2a, men type II

2528 clinical trials for this condition and its sub-types.

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