von Hippel-Lindau Disease


Angiomatoses, Familial Cerebello-Retinal

Angiomatoses, Familial Cerebelloretinal

Angiomatosis Retinae

Angiomatosis, Familial Cerebello-Retinal

Angiomatosis, Familial Cerebelloretinal

Cerebello-Retinal Angiomatoses, Familial

Cerebello-Retinal Angiomatosis, Familial

Cerebelloretinal Angiomatoses, Familial

Cerebelloretinal Angiomatosis, Familial

Familial Cerebello Retinal Angiomatosis

Familial Cerebello-Retinal Angiomatoses

Familial Cerebello-Retinal Angiomatosis

Familial Cerebelloretinal Angiomatoses

Familial Cerebelloretinal Angiomatosis

Hippel Lindau Disease

Hippel-Lindau Disease

Lindau Disease

Lindau's Disease

Lindau's Diseases

Lindaus Disease

Retinae, Angiomatosis

Syndrome, VHL

Syndrome, von Hippel-Lindau

Syndromes, VHL

VHL Syndrome

VHL Syndromes

von Hippel Lindau Disease

von Hippel Lindau Syndrome

von Hippel-Lindau Syndrome

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.