autosomal dominant disease eye disorder von Hippel-Lindau disease https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/9178 https://rarediseases.info.nih.gov/diseases/7855/von-hippel-lindau-disease https://www.malacards.org/card/von_hippel_lindau_syndrome NANDO:2200408 MedDRA:10047716 MESH:D006623 Von Hippel-Lindau syndrome, Modifiers of NCIT:C3105 VHL syndrome Von Hippel-Lindau syndrome NORD:1830 cerebroretinal angiomatosis An autosomal dominant disorder caused by pathogenic variants in the VHL gene, leading to an increased risk of various benign and malignant tumors, including hemangioblastomas, retinal hemangiomas, endolymphatic sac tumors, renal cell carcinoma, and pheochromocytomas. von Hippel-Lindau syndrome Von Hippel-Lindau syndrome (VHL) OMIM:193300 von Hippel-Lindau syndrome, modifier of MONDO:0008667 GARD:0007855 NANDO:2200829 von Hippel-Lindau disease UMLS:C0019562 Lindau disease VHL-related von Hippel-Lindau disease DOID:14175 Orphanet:892 SCTID:46659004 VHL icd11.foundation:1985408165 ICD9:759.6 Von Hippel Lindau disease MEDGEN:42458 familial cerebelloretinal angiomatosis multiple polyglandular tumor obsolete genetic central nervous system and retinal vascular disease obsolete inherited nervous system cancer-predisposing syndrome obsolete inherited renal cancer-predisposing syndrome familial cystic renal disease developmental defect during embryogenesis obsolete disorder of central nervous system or retinal vasculature disorder of development or morphogenesis neurocutaneous syndrome hereditary neurological disease