_:b730688 _:b795399 . _:b795403 _:b795404 . "A rare inherited disorder in which blood vessels grow abnormally in the eyes, brain, spinal cord, adrenal glands, or other parts of the body. People with von Hippel-Lindau syndrome have a higher risk of developing some types of cancer.NCI-GLOSS" . _:b795402 _:b795403 . _:b723118 . _:b723117 . _:b723112 . _:b795401 _:b795402 . _:b723119 . "Von Hippel-Lindau Syndrome"^^ . _:b795400 _:b795401 . "Disease or Syndrome"^^ . _:b723116 . _:b723120 . _:b723115 . . _:b723117 . _:b795399 _:b795400 . _:b723113 . _:b723116 . _:b795399 _:b723112 . _:b723113 . _:b723120 . _:b723114 . _:b723120 . "Cerebroretinal AngiomatosisSYNCI" . "Von_Hippel-Lindau_Syndrome"^^ . _:b641209 . _:b723117 . _:b795401 _:b723114 . _:b795407 _:b723120 . _:b795407 . _:b723116 . _:b795400 _:b723113 . _:b723119 . "Von Hippel-Lindau Syndrome"^^ . "C0019562"^^ . _:b723118 . _:b723118 . _:b795402 _:b723115 . "An inherited familial cancer syndrome which is characterized by development of capillary hemangioblastomas of the central nervous system and retina; clear cell renal carcinoma; pheochromocytoma; pancreatic tumors; and inner ear tumors. The syndrome is associated with germline mutations of the VHL tumor suppressor gene, located on chromosome 3p25-26. Symptoms of VHL syndrome may not be apparent until the third decade of life. CNS hemangioblastoma is the most common cause of death, followed by clear cell renal cell carcinoma. --2004NCI" . _:b795403 _:b723116 . . _:b641209 _:b730688 . _:b795404 _:b723117 . _:b795406 _:b795407 . _:b795405 _:b723118 . "Von Hippel-Lindau SyndromePTNCI" . _:b723114 . _:b723115 . _:b641209 . _:b795406 _:b723119 . _:b795404 _:b795405 . _:b723115 . "VHL syndromePTNCI-GLOSSCDR0000575486" . _:b795405 _:b795406 . "Von Hippel-Lindau DiseaseSYNCI" . _:b723112 . _:b723119 . "von Hippel-Lindau syndromePTNCI-GLOSSCDR0000045563" . _:b723114 . "C3105"^^ . _:b723112 . _:b730688 . "Von Hippel-Lindau Syndrome (VHL)SYNCI" . _:b723113 .