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last update : 19/07/2006
Symbol MEN1
Location 11q13.2
Name endocrine neoplasia, multiple, type 1
Other name(s)
  • endocrine adenomatosis, multiple . Wermer syndrome (MEN1 defect)
  • Corresponding gene MEN1
    related resource Multiple Endocrine Neoplasia type 1 Mutation Database
    Other symbol(s) MEA1
    Main clinical features
  • hyperparathyroidism, gastrinoma somatotrophinoma, prolactinoma, including somatic mutations in sporadic neuroendocrine and pancreatic tumors, and carcinoid tumors of lungs and in fore foregut neoplasms, excluding the sporadic hyperplastic or neoplastic lesions of the adrenal cortex
  • Genetic determination autosomal dominant
    Related entries Zollinger-Ellison syndrome and lipoma and angiofibroma sporadic
    Function/system disorder endocrinology
    Type disease
    Gene product
    Name menin defect (MEN1)