multiple endocrine neoplasia III
syndrome characterized by tumors found in MEN2, tall, thin habitus, prominent lips, and neuromas of the tongue and eyelids; autosomal dominant inheritance, caused by mutation in the RET oncogene on 10q.
Synonym(s): multiple endocrine neoplasia IIB
Search Stedman's Medical Dictionary
Examples: glitazone, GI cocktail, etc.