Visão selecionada em Inglês
| Descritor em português: | Doença de von Hippel-Lindau | ||||||
| Descritor em inglês: | von Hippel-Lindau Disease | ||||||
| Descritor em espanhol: |
Enfermedad de von Hippel-Lindau
| ||||||
| Descritor em francês: | Maladie de von Hippel-Lindau | ||||||
| Termo(s) alternativo(s): |
Angiomatoses, Familial Cerebello-Retinal Angiomatoses, Familial Cerebelloretinal Angiomatosis Retinae Angiomatosis, Familial Cerebello-Retinal Angiomatosis, Familial Cerebelloretinal Cerebello-Retinal Angiomatoses, Familial Cerebello-Retinal Angiomatosis, Familial Cerebelloretinal Angiomatoses, Familial Cerebelloretinal Angiomatosis, Familial Familial Cerebello Retinal Angiomatosis Familial Cerebello-Retinal Angiomatoses Familial Cerebello-Retinal Angiomatosis Familial Cerebelloretinal Angiomatoses Familial Cerebelloretinal Angiomatosis Hippel Lindau Disease Hippel-Lindau Disease Lindau Disease Lindau's Disease Lindau's Diseases Lindaus Disease VHL Syndrome VHL Syndromes von Hippel Lindau Disease von Hippel Lindau Syndrome von Hippel-Lindau Syndrome |
||||||
| Código(s) hierárquico(s): |
C10.562.925 C14.907.077.925 C16.131.077.245.750 C16.320.184.750 |
||||||
| Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D006623 | ||||||
| Nota de escopo: | An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions. |
||||||
| 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 |
||||||
| Nota MeSH pública: | 2008; see HIPPEL-LINDAU DISEASE 1991-2007; see ANGIOMATOSIS 1975-1990 |
||||||
| Nota histórica: | 2008 (1975) |
||||||
| Versão alternativa: | VON HIPPEL LINDAU DIS |
||||||
| Identificador DeCS: | 6781 | ||||||
| ID do descritor: | D006623 | ||||||
| Classificação da NLM: | QS 677 | ||||||
| Documentos indexados na Biblioteca Virtual em Saúde (BVS): | Clique aqui para acessar os documentos da BVS | ||||||
| Data de estabelecimento: | 01/01/1991 | ||||||
| Data de entrada: | 01/01/1999 | ||||||
| Data de revisão: | 14/12/2017 |
|
|
von Hippel-Lindau Disease
- Conceito preferido
| Identificador do conceito |
M0010373 |
| Nota de escopo | An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions. |
| Termo preferido | von Hippel-Lindau Disease |
| Termo(s) alternativo(s) |
Angiomatoses, Familial Cerebello-Retinal Angiomatoses, Familial Cerebelloretinal Angiomatosis Retinae Angiomatosis, Familial Cerebello-Retinal Angiomatosis, Familial Cerebelloretinal Cerebello-Retinal Angiomatoses, Familial Cerebello-Retinal Angiomatosis, Familial Cerebelloretinal Angiomatoses, Familial Cerebelloretinal Angiomatosis, Familial Familial Cerebello Retinal Angiomatosis Familial Cerebello-Retinal Angiomatoses Familial Cerebello-Retinal Angiomatosis Familial Cerebelloretinal Angiomatoses Familial Cerebelloretinal Angiomatosis Hippel Lindau Disease Hippel-Lindau Disease Lindau Disease Lindau's Disease Lindau's Diseases Lindaus Disease VHL Syndrome VHL Syndromes von Hippel Lindau Disease von Hippel Lindau Syndrome von Hippel-Lindau Syndrome |
Queremos a sua opinião sobre o novo sitio web do DeCS/MeSH
Convidamos-lhe a responder a uma pesquisa que não levará mais que 3 minutos
Ir para pesquisa
