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pubmed-article:7985090pubmed:abstractTextvon Hippel-Lindau disease is an autosomal dominant disorder characterized by the development of hemangioblastomas in the cerebellum, spinal cord, and retina, renal cell carcinoma and cysts, pancreatic cysts, and pheochromocytoma.lld:pubmed
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pubmed-article:7985090pubmed:articleTitlePheochromocytoma as the first manifestation of von Hippel-Lindau disease.lld:pubmed
pubmed-article:7985090pubmed:affiliationEPHE, La Salpêtrière, Paris, France.lld:pubmed
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