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(Q3347154)

English

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

  • MEN type I
  • Wermer syndrome
  • Wermer's syndrome
  • Multiple Endocrine Adenomatosis
  • MEN1
  • Mea 1
  • Multiple Endocrine Neoplasia Type 1
  • MEN1 syndrome
  • Men1 Somatic Mutations
  • MEA Type I
  • Endocrine Adenomatosis, Multiple
  • MULTIPLE ENDOCRINE NEOPLASIA, TYPE I; MEN1
  • Multiple Endocrine Adenomatosis, Type I
  • Multiple Endocrine Adenomatosis Type 1
  • Men 1
  • MEN Type 1
  • MULTIPLE ENDOCRINE NEOPLASIA, TYPE I
  • MEA Type 1
  • Multiple Endocrine Adenomatosis Type I
  • Multiple Endocrine Neoplasia Type I
  • multiple endocrine neoplasia type 1 syndrome
  • Endocrine adenomatosis multiple
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