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neoplázia endokrinná mnohopočetná, typ 1

  1. Record numberd018761
    Date06.06.2025
    TypeM - MESH
    Topical termneoplázia endokrinná mnohopočetná, typ 1
    Other termEnglish (Pseudonym) Neoplasia, Multiple Endocrine Type 1
    English (Pseudonym) Neoplasms, Multiple Endocrine Type 1
    English (Pseudonym) Wermer Syndrome
    Slovak (Pseudonym) nádory endokrinné mnohopočetné, typ 1
    Slovak (Pseudonym) Wermerov syndróm
    See also(Later heading) hyperparatyreoidizmus
    (Later heading) Zollingerov-Ellisonov syndróm
    (Later heading) gastrinóm
    UDCC04.588.322.400.500C04.651.600.500C04.700.630.500C16.320.700.630.500C19.344.400.500
    NoteA form of multiple endocrine neoplasia that is characterized by the combined occurrence of tumors in the PARATHYROID GLANDS, the PITUITARY GLAND, and the PANCREATIC ISLETS. The resulting clinical signs include HYPERPARATHYROIDISM; HYPERCALCEMIA; HYPERPROLACTINEMIA; CUSHING DISEASE; GASTRINOMA; and ZOLLINGER-ELLISON SYNDROME. This disease is due to loss-of-function of the MEN1 gene, a tumor suppressor gene (GENES, TUMOR SUPPRESSOR) on CHROMOSOME 11 (Locus: 11q13).
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Number of the records: 1  

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