Visão selecionada em Inglês
Descritor em português: | Síndrome de Peutz-Jeghers | ||||
Descritor em inglês: | Peutz-Jeghers Syndrome | ||||
Descritor em espanhol: |
Síndrome de Peutz-Jeghers
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Descritor em francês: | Syndrome de Peutz-Jeghers | ||||
Termo(s) alternativo(s): |
Hamartomatous Intestinal Polyposes Hamartomatous Intestinal Polyposis Intestinal Polyposes, Hamartomatous Intestinal Polyposis, Hamartomatous Lentiginoses, Perioral Lentiginosis, Perioral Perioral Lentiginoses Perioral Lentiginosis Periorificial Lentiginosis Syndrome Periorificial Lentiginosis Syndromes Peutz Jegher's Syndrome Peutz Jeghers Polyposis Peutz Jeghers Syndrome Peutz-Jegher Syndrome Peutz-Jegher's Syndrome Peutz-Jeghers Polyposis Polyposes, Hamartomatous Intestinal Polyposis, Hamartomatous Intestinal Polyposis, Peutz-Jeghers Polyps and Spots Syndrome Polyps-and-Spots Syndrome Polyps-and-Spots Syndromes Syndrome, Periorificial Lentiginosis Syndrome, Peutz-Jegher's Syndrome, Peutz-Jeghers Syndrome, Polyps-and-Spots Syndromes, Periorificial Lentiginosis Syndromes, Polyps-and-Spots |
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Código(s) hierárquico(s): |
C04.700.633 C06.405.469.578.750 C16.320.700.667 C17.800.621.430.530.550.625 |
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Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D010580 | ||||
Nota de escopo: | A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits. |
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Qualificadores permitidos: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification 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 SU surgery TH therapy UR urine VE veterinary VI virology |
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Nota MeSH pública: | 65; was see under POLYPI (now POLYPS) 1963-64 |
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Nota histórica: | 65; was see under POLYPI (now POLYPS) 1963-64 |
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Identificador DeCS: | 22610 | ||||
ID do descritor: | D010580 | ||||
Documentos indexados na Biblioteca Virtual em Saúde (BVS): | Clique aqui para acessar os documentos da BVS | ||||
Data de estabelecimento: | 01/01/1965 | ||||
Data de entrada: | 01/01/1999 | ||||
Data de revisão: | 29/06/2018 |
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DISEASES
Neoplasms [C04]Neoplasms
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Peutz-Jeghers Syndrome
- Conceito preferido
Identificador do conceito |
M0016441 |
Nota de escopo | A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits. |
Termo preferido | Peutz-Jeghers Syndrome |
Termo(s) alternativo(s) |
Hamartomatous Intestinal Polyposes Hamartomatous Intestinal Polyposis Intestinal Polyposes, Hamartomatous Intestinal Polyposis, Hamartomatous Lentiginoses, Perioral Lentiginosis, Perioral Perioral Lentiginoses Perioral Lentiginosis Periorificial Lentiginosis Syndrome Periorificial Lentiginosis Syndromes Peutz Jegher's Syndrome Peutz Jeghers Polyposis Peutz Jeghers Syndrome Peutz-Jegher Syndrome Peutz-Jegher's Syndrome Peutz-Jeghers Polyposis Polyposes, Hamartomatous Intestinal Polyposis, Hamartomatous Intestinal Polyposis, Peutz-Jeghers Polyps and Spots Syndrome Polyps-and-Spots Syndrome Polyps-and-Spots Syndromes Syndrome, Periorificial Lentiginosis Syndrome, Peutz-Jegher's Syndrome, Peutz-Jeghers Syndrome, Polyps-and-Spots Syndromes, Periorificial Lentiginosis Syndromes, Polyps-and-Spots |
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