PedAM
Pediatric Disease Annotations & Medicines
| Disease | von hippel-lindau syndrome |
| Phenotype | C0019562|von hippel-lindau syndrome (vhl) |
| Sentences | 1 |
| PubMedID- 26557756 | von hippel-lindau syndrome (vhl) is an autosomal, dominantly inherited disease in which the most frequent tumours are retinal and central nervous system haemangioblastomas, clear cell renal carcinoma, phaeochromocytoma and pancreatic cystic and/or endocrine tumours [61–64]. |
Page: 1