congenital nervous system disorder von Hippel-Lindau disease DOID:14175 GARD:0007855 Hippel Lindau syndrome ICD10:Q85.8 ICD9:759.6 Lindau disease MESH:D006623 MONDO:0008667 MedDRA:10047716 NCIT:C3105 OMIM:193300 Orphanet:892 SCTID:46659004 UMLS:C0019562 VHL VHL syndrome VON Hippel-Lindau syndrome Von Hippel Lindau disease Von Hippel-Lindau disease (VHL) is a familial cancer predisposition syndrome associated with a variety of malignant and benign neoplasms, most frequently retinal, cerebellar, and spinal hemangioblastoma, renal cell carcinoma (RCC), and pheochromocytoma. Von Hippel-Lindau syndrome Von Hippel-Lindau syndrome (VHL) Von Hippel-Lindau syndrome, Modifiers of cerebroretinal angiomatosis familial cerebelloretinal angiomatosis https://rarediseases.info.nih.gov/diseases/7855/von-hippel-lindau-disease von Hippel-Lindau syndrome multiple polyglandular tumor syndromic developmental defect of the eye genetic central nervous system and retinal vascular disease inherited nervous system cancer-predisposing syndrome inherited renal cancer-predisposing syndrome familial cystic renal disease malformation syndrome with hamartosis rare disease with glaucoma as a major feature neurocutaneous syndrome