Other terms
von Hippel Lindau Disease,Familial Cerebello-Retinal Angiomatosis,Angiomatoses, Familial Cerebello-Retinal,Angiomatosis, Familial Cerebello-Retinal,Cerebello-Retinal Angiomatoses, Familial,Cerebello-Retinal Angiomatosis, Familial,Familial Cerebello Retinal Angiomatosis,Familial Cerebello-Retinal Angiomatoses,Hippel-Lindau Disease,Hippel Lindau Disease,Lindau's Disease,Lindau's Diseases,Lindaus Disease,von Hippel-Lindau Syndrome,Syndrome, von Hippel-Lindau,von Hippel Lindau Syndrome,Cerebelloretinal Angiomatosis, Familial,Angiomatoses, Familial Cerebelloretinal,Angiomatosis, Familial Cerebelloretinal,Cerebelloretinal Angiomatoses, Familial,Familial Cerebelloretinal Angiomatoses,Familial Cerebelloretinal Angiomatosis,Lindau Disease
Description
von Hippel-Lindau Disease: An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions.
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