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Related to von Hippel-Lindau disease: tuberous sclerosis, pheochromocytoma, neurofibromatosis, hemangioblastoma
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Von Hippel-Lindau disease is progressive, which means new tumours could develop at any time, but she refuses to let that hold her back.
Molecular cytogenetic characterization of early and late renal cell carcinomas in von Hippel-Lindau disease.
Inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene causes a hereditary cancer syndrome called von Hippel-Lindau disease.
Von Hippel-Lindau disease is an autosomal dominant disorder that shows an incomplete penetrance (the gene is inherited, but not always expressed).
Differential grading of endolymphatic sac tumor by virtue of von Hippel-Lindau disease status.
Two cases of bile duct NET, reported in patients with von Hippel-Lindau disease, may be related to the propensity for patients with von Hippel-Lindau syndrome to develop neuroendocrine tumors.