|
gptkbp:instanceOf
|
gptkb:disease
brain tumor
|
|
gptkbp:affects
|
gptkb:adrenal_gland
|
|
gptkbp:associatedWith
|
gptkb:Neurofibromatosis_type_1
gptkb:Von_Hippel-Lindau_disease
gptkb:Multiple_Endocrine_Neoplasia_type_2
|
|
gptkbp:canBeBenign
|
true
|
|
gptkbp:canBeBilateral
|
true
|
|
gptkbp:canBeExtraAdrenal
|
true
|
|
gptkbp:canBeMalignant
|
true
|
|
gptkbp:cause
|
gptkb:orthostatic_hypotension
anxiety
constipation
headache
hypertension
tremor
weight loss
sweating
palpitations
flushing
panic attacks
hyperglycemia
visual disturbances
paroxysmal hypertension
|
|
gptkbp:diagnosedBy
|
gptkb:CT_scan
MRI
plasma metanephrines
urine metanephrines
|
|
gptkbp:extraAdrenalForm
|
paraganglioma
|
|
gptkbp:firstDescribed
|
1886
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
Pheochromocytoma
|
|
gptkbp:ICD-10_code
|
C74.1
|
|
gptkbp:MeSH_ID
|
D010673
|
|
gptkbp:namedFor
|
gptkb:Ludwig_Pick
|
|
gptkbp:occurredIn
|
adults
children
|
|
gptkbp:OMIM
|
171300
|
|
gptkbp:originatedIn
|
chromaffin cells
|
|
gptkbp:prevalence
|
rare
|
|
gptkbp:riskFactor
|
family history
genetic disorder
|
|
gptkbp:secretes
|
dopamine
norepinephrine
epinephrine
|
|
gptkbp:treatment
|
beta blockers
surgical removal
alpha blockers
|
|
gptkbp:bfsParent
|
gptkb:Adrenal_Gland
|
|
gptkbp:bfsLayer
|
6
|