Von Hippel-Lindau disease (Q61506): Difference between revisions
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A doença de Von Hippel-Lindau (VHL) é uma síndrome familiar com predisposição ao câncer associada a uma variedade de neoplasias malignas e benignas, mais frequentemente hemangioblastoma da retina, do cerebelo e da medula espinhal, carcinoma de células renais e feocromocitoma. | |||
| description / en | description / en | ||
Von Hippel-Lindau disease (VHL) is a familial cancer predisposition syndrome associated with a variety of malignant and benign neoplasms, most frequently retinal, cerebellar, and spinal hemangioblastoma, renal cell carcinoma (RCC), and pheochromocytoma. | |||
Revision as of 08:59, 14 August 2026
Von Hippel-Lindau disease (VHL) is a familial cancer predisposition syndrome associated with a variety of malignant and benign neoplasms, most frequently retinal, cerebellar, and spinal hemangioblastoma, renal cell carcinoma (RCC), and pheochromocytoma.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1985408165 |
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| English | Von Hippel-Lindau disease |
Von Hippel-Lindau disease (VHL) is a familial cancer predisposition syndrome associated with a variety of malignant and benign neoplasms, most frequently retinal, cerebellar, and spinal hemangioblastoma, renal cell carcinoma (RCC), and pheochromocytoma. |
