Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

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

2775 clinical trials for this condition and its sub-types, 4 tagged with Multiple endocrine neoplasia type 2A itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by