A form of multiple endocrine neoplasia that is characterized by the combined occurrence of tumors in the , the , and the . The resulting clinical signs include ; ; ; ; ; and . This disease is due to loss-of-function of the MEN1 gene, a tumor suppressor gene () on (Locus: 11q13).
Polyadénomatose endocrinienne de type 1 /
Syndrome de Wermer /
Adénomatose endocrinienne multiple de type 1 /
NEM 1 /