Von Hippel-Lindau disease (Q61506): Difference between revisions
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13 August 2026
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Latest 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. |
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CID11:ID_1985408165
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dki-india-ID_1985408165
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Concluído
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13 August 2026
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