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Descritor em português: | Neurofibromatoses | ||||
Descritor em inglês: | Neurofibromatoses | ||||
Descritor em espanhol: |
Neurofibromatosis
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Descritor em francês: | Neurofibromatoses | ||||
Termo(s) alternativo(s): |
Multiple Neurofibroma Multiple Neurofibromas Neurofibroma, Multiple Neurofibromas, Multiple Neurofibromatosis Neurofibromatosis 3 Neurofibromatosis 3s Neurofibromatosis Syndrome Neurofibromatosis Syndromes Neurofibromatosis Type 3 Neurofibromatosis Type 3s Syndrome, Neurofibromatosis Syndromes, Neurofibromatosis Type 3, Neurofibromatosis |
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Código(s) hierárquico(s): |
C04.557.580.600.580.590 C04.700.631 C10.562.600 C10.574.500.549 C16.320.400.560 C16.320.700.633 |
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Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D017253 | ||||
Nota de escopo: | A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72) |
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Nota de indexação: | multiple neurofibromas; specifics are available |
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Qualificadores permitidos: |
BL blood CF cerebrospinal fluid 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 SU surgery TH therapy UR urine VE veterinary VI virology |
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Nota MeSH pública: | 2000; see NEUROFIBROMATOSIS 1993-1999 |
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Nota histórica: | 2000(1993) |
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Identificador DeCS: | 30639 | ||||
ID do descritor: | D017253 | ||||
Classificação da NLM: | QZ 380 | ||||
Documentos indexados na Biblioteca Virtual em Saúde (BVS): | Clique aqui para acessar os documentos da BVS | ||||
Data de estabelecimento: | 01/01/1993 | ||||
Data de entrada: | 22/05/1992 | ||||
Data de revisão: | 29/06/2018 |
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DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Neoplasms [C04]Neoplasms
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Neurofibromatoses
- Conceito preferido
Neurofibromatosis 3
- Mais específico
Identificador do conceito |
M0026175 |
Nota de escopo | A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72) |
Termo preferido | Neurofibromatoses |
Termo(s) alternativo(s) |
Multiple Neurofibroma Multiple Neurofibromas Neurofibroma, Multiple Neurofibromas, Multiple Neurofibromatosis Neurofibromatosis Syndrome Neurofibromatosis Syndromes Syndrome, Neurofibromatosis Syndromes, Neurofibromatosis |
Identificador do conceito |
M0337469 |
Termo preferido | Neurofibromatosis 3 |
Termo(s) alternativo(s) |
Neurofibromatosis 3s Neurofibromatosis Type 3 Neurofibromatosis Type 3s Type 3, Neurofibromatosis |
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