|
gptkbp:instanceOf
|
gptkb:brain_tumor
gptkb:rare_disease
|
|
gptkbp:associatedWith
|
gptkb:Von_Hippel-Lindau_disease
|
|
gptkbp:canBeBenign
|
true
|
|
gptkbp:hasLocation
|
gptkb:spinal_cord
gptkb:cerebellum
retina
central nervous system
|
|
gptkbp:hasMedianAgeOfOnset
|
30-40 years
|
|
gptkbp:hasOrphanetID
|
ORPHA:310
|
|
gptkbp:hasRecurrenceRisk
|
possible, especially with incomplete resection
|
|
gptkbp:histology
|
highly vascular tumor with stromal cells
|
|
gptkbp:ICD-10_code
|
D18.0
|
|
gptkbp:isVascular
|
true
|
|
gptkbp:OMIM
|
613537
|
|
gptkbp:originatedIn
|
stromal cell
vascular endothelial cell
|
|
gptkbp:prevalence
|
rare
|
|
gptkbp:prognosis
|
good with complete resection
|
|
gptkbp:riskFactor
|
Von Hippel-Lindau gene mutation
|
|
gptkbp:symptom
|
nausea
vomiting
headache
ataxia
|
|
gptkbp:synonym
|
capillary hemangioblastoma
retinal hemangioblastoma
|
|
gptkbp:treatment
|
gptkb:radiation_therapy
surgical resection
|
|
gptkbp:bfsParent
|
gptkb:Von_Hippel-Lindau_Disease
gptkb:von_Hippel–Lindau_disease
gptkb:VHL
|
|
gptkbp:bfsLayer
|
7
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
hemangioblastoma
|