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head and neck paragangliomas
URI:
https://gptkb.org/entity/head_and_neck_paragangliomas
GPTKB entity
Statements (50)
Predicate
Object
gptkbp:instanceOf
gptkb:disease
brain tumor
gptkbp:age
adults
gptkbp:associatedWith
SDH gene mutations
hereditary paraganglioma syndromes
gptkbp:canBe
familial
sporadic
gptkbp:complication
malignant transformation
cranial nerve dysfunction
vascular involvement
gptkbp:diagnosedBy
gptkb:CT_scan
MRI
biopsy
angiography
gptkbp:firstDescribed
early 20th century
gptkbp:gender
female predominance
gptkbp:histology
Zellballen pattern
https://www.w3.org/2000/01/rdf-schema#label
head and neck paragangliomas
gptkbp:ICD-10_code
gptkb:D35.6
gptkbp:location
head
neck
gptkbp:marking
gptkb:chromogranin_A
gptkb:S-100_protein
synaptophysin
gptkbp:maySecrete
gptkb:catecholamines
gptkbp:originatedIn
gptkb:paraganglionic_tissue
gptkbp:prevalence
rare
gptkbp:rarelyMetastasize
true
gptkbp:riskFactor
family history
SDHB mutation
SDHC mutation
SDHD mutation
gptkbp:subspecies
paraganglioma
Neuroendocrine Tumor
gptkbp:symptom
hearing loss
cranial nerve palsy
pulsatile tinnitus
gptkbp:synonym
gptkb:chemodectoma
glomus tumor
gptkbp:treatment
astronomer
surgery
radiation therapy
gptkbp:website
gptkb:carotid_body
vagal body
glomus jugulare
glomus tympanicum
jugulotympanic region
gptkbp:bfsParent
gptkb:Hereditary_paraganglioma-pheochromocytoma_syndrome
gptkb:hereditary_paraganglioma-pheochromocytoma_syndrome
gptkbp:bfsLayer
8