Visão selecionada em Inglês
Descritor em português: | Neoplasia Endócrina Múltipla Tipo 1 | ||||||
Descritor em inglês: | Multiple Endocrine Neoplasia Type 1 | ||||||
Descritor em espanhol: |
Neoplasia Endocrina Múltiple Tipo 1
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Descritor em francês: | Néoplasie endocrinienne multiple de type 1 | ||||||
Termo(s) alternativo(s): |
Multiple Endocrine Neoplasia Type I Multiple Endocrine Neoplasms Type 1 Neoplasia, Multiple Endocrine Type 1 Neoplasms, Multiple Endocrine Type 1 Neoplasms, Multiple Endocrine Type I Wermer Syndrome |
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Código(s) hierárquico(s): |
C04.588.322.400.500 C04.651.600.500 C04.700.630.500 C16.320.700.630.500 C19.344.400.500 |
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Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D018761 | ||||||
Nota de escopo: | A 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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Nota de indexação: | coordinate IM with specific endocrine/neoplasm pre-coordinates (IM) + specific histological type (IM) if pertinent |
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Qualificadores permitidos: |
BL blood BS blood supply CF cerebrospinal fluid CH chemistry CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SC secondary SU surgery TH therapy UL ultrastructure UR urine VE veterinary VI virology |
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Indexação Anterior: |
Multiple Endocrine Neoplasia (1972-1994) |
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Nota MeSH pública: | 95; MEA I, MEN I, & WERMER SYNDROME were see NEOPLASMS, MULTIPLE ENDOCRINE 1983-94 |
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Nota Online: | use MULTIPLE ENDOCRINE NEOPLASIA to search MEA I, MEN I, & WERMER SYNDROME 1983-94 |
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Nota histórica: | 95; MEA I, MEN I, & WERMER SYNDROME were see NEOPLASMS, MULTIPLE ENDOCRINE 1983-94 |
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Versão alternativa: | MULTIPLE ENDOCRINE NEOPL TYPE 1 |
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Identificador DeCS: | 32134 | ||||||
ID do descritor: | D018761 | ||||||
Documentos indexados na Biblioteca Virtual em Saúde (BVS): | Clique aqui para acessar os documentos da BVS | ||||||
Data de estabelecimento: | 01/01/1995 | ||||||
Data de entrada: | 23/05/1994 | ||||||
Data de revisão: | 24/02/2017 |
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Neoplasms [C04]Neoplasms -
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Neoplasms [C04]Neoplasms -
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Neoplasms [C04]Neoplasms
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Multiple Endocrine Neoplasia Type 1
- Conceito preferido
Identificador do conceito |
M0028096 |
Nota de escopo | A 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). |
Termo preferido | Multiple Endocrine Neoplasia Type 1 |
Termo(s) alternativo(s) |
Multiple Endocrine Neoplasia Type I Multiple Endocrine Neoplasms Type 1 Neoplasia, Multiple Endocrine Type 1 Neoplasms, Multiple Endocrine Type 1 Neoplasms, Multiple Endocrine Type I Wermer Syndrome |
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