VHL

(redirected from Von Hippel-Lindau)
Also found in: Medical.
AcronymDefinition
VHLVon Hippel-Lindau (disease)
VHLVery High Level Language
VHLVirtual Health Library (online information resource; Latin-American and Caribbean Center on Health Sciences Information)
VHLvon Hippel-Lindau gene
VHLVista Higher Learning, Inc. (language program publisher; Boston, MA)
VHLVirax Holdings Limited (finance company)
VHLVan Hasseltlaan (Delft University of Technology, Netherlands)
VHLVallejo-Henry-Lecuyer (French musical trio)
VHLVoyages Haute Loire (French travel company)
References in periodicals archive ?
M2 EQUITYBITES-February 12, 2018-Elsevier signs partnership with VHL Alliance on PracticeUpdateFree virtual resource about von Hippel-Lindau Disease
M2 PHARMA-February 12, 2018-Elsevier signs partnership with VHL Alliance on PracticeUpdateFree virtual resource about von Hippel-Lindau Disease
The tumor is very rare in the sporadic form, but more often associated with Von Hippel-Lindau disease.
Von Hippel-Lindau (VHL) disease a familial cancer syndrome characterized by benign or malignant tumors and cystic lesions affecting multiple systems.
Tobacco is the most predisposing risk factor; other risk factors include cystic disease, tuberous sclerosis, von Hippel-Lindau syndrome, etc.
1,2 HMBs can arise sporadically or can be associated with von Hippel-Lindau (VHL) disease.
Linzie Offord suffers from Von Hippel-Lindau syndrome (VHL), which affects internal organs and causes tumours to grow around the body.
At seven Andy was found to have Von Hippel-Lindau syndrome, where tumours develop and attack organs.
Text-word combinations included familial RCC, von Hippel-Lindau, hereditary papillary renal cancer, hereditary leiomyomatosis, hereditary paragangliomas and pheochromocytomas, Birt-Hogg-Dube, and tuberous sclerosis complex.
9] Human genes: TH, tyrosine hydroxylase; DBH, dopamine beta-hydroxylase; PNMT, phenylethanolamine N-methyltransferase; SDH3, succinate dehydrogenase complex iron sulfur subunit B; SDHD, succinate dehydrogenase complex subunit D; VHL, von Hippel-Lindau tumor suppressor; RET, ret proto-oncogene.
For example, in von Hippel-Lindau syndrome, (5) it appears that the incidence of pancreatic involvement by renal cell carcinoma is less than the general population, whereas in the setting of Birt-Hogg-Dube syndrome, (6) the scant data suggest that incidence may be the same as that in the general population.
Her family history was significant for von Hippel-Lindau disease (VHL), affecting her father and paternal grandmother.