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Medical Term:

multiple endocrine neoplasia II

 

Definition: syndrome associated with pheochromocytoma, parathyroid adenoma and medullary thyroid carcinoma; autosomal dominant inheritance, caused by mutation in the RET oncogene on chromosome 10q.

© Copyright 2016 Wolters Kluwer. All Rights Reserved. Review Date: Sep 19, 2016.
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