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Multiple endocrine neoplasia type 1

autosomal dominant disease that has material basis in a mutation in the MEN1 tumor suppressor gene and is characterized by over active endocrine glands frequently involving tumors of the parathyroid glands, the pituitary gland, and the pancreas

Pronunciation
/ˈmʌltɪpəl ˈɛndəʊkrɪn ˌniːəʊˈpleɪzɪə tʌɪp 1/
/ˈməltəpəl ˈɛndəkrən ˌnioʊˈpleɪʒiə taɪp 1/