Concept information
Término preferido
von Hippel-Lindau Disease
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Tipo
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mesh:Descriptor
Definición
- 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.
Concepto genérico
Etiquetas alternativas
- Angiomatosis Retinae
- Cerebelloretinal Angiomatosis, Familial
- Familial Cerebello-Retinal Angiomatosis
- Hippel-Lindau Disease
- Lindau Disease
- Lindau's Disease
- VHL Syndrome
- von Hippel-Lindau Syndrome
En otras lenguas
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francés
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Angiomatose cérébello-rétinienne de von Hippel-Lindau
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Angiomatose cérébellorétinienne de von Hippel-Lindau
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Angiomatose cérébellorétinienne familiale
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Angiomatose rétino-cérébelleuse de von Hippel-Lindau
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Angiomatose rétinocérébelleuse de von Hippel-Lindau
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Maladie de Lindau
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Syndrome de VHL
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Syndrome de von Hippel-Lindau
URI
http://data.loterre.fr/ark:/67375/JVR-XP9XZV7W-T
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