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.

Descriptor ID	D006623
MeSH Number(s)	C10.562.925 C14.907.077.925
Concept/Terms	von Hippel-Lindau Disease von Hippel-Lindau Disease 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 von Hippel-Lindau Syndrome Syndrome, von Hippel-Lindau von Hippel Lindau Syndrome Lindau Disease Lindau's Disease Lindau's Diseases Lindaus Disease Cerebelloretinal Angiomatosis, Familial Angiomatoses, Familial Cerebelloretinal Angiomatosis, Familial Cerebelloretinal Cerebelloretinal Angiomatoses, Familial Familial Cerebelloretinal Angiomatoses Familial Cerebelloretinal Angiomatosis Hippel-Lindau Disease Hippel Lindau Disease

Below are MeSH descriptors whose meaning is more general than "von Hippel-Lindau Disease".

Below are MeSH descriptors whose meaning is related to "von Hippel-Lindau Disease".

Below are MeSH descriptors whose meaning is more specific than "von Hippel-Lindau Disease".