hereditary papillary renal carcinoma
GPTKB entity
Statements (21)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:renal_cell_carcinoma_subtype
gptkb:hereditary_cancer_syndrome |
| gptkbp:associatedWith |
type 1 papillary renal cell carcinoma
|
| gptkbp:characteristic |
multiple bilateral papillary renal cell carcinomas
|
| gptkbp:firstDescribed |
1994
|
| gptkbp:hasClinicalFeature |
multiple tumors
bilateral kidney involvement onset in adulthood |
| gptkbp:hasGeneticBasis |
MET gene mutation
|
| gptkbp:hasMolecularFormula |
loss of Y chromosome in males
trisomy 17 trisomy 7 |
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:OMIM |
605074
|
| gptkbp:prevalence |
rare
|
| gptkbp:riskFactor |
increased risk of kidney cancer
|
| gptkbp:synonym |
HPRC
hereditary papillary renal cell carcinoma |
| gptkbp:treatment |
surgical resection
active surveillance |
| https://www.w3.org/2000/01/rdf-schema#label |
hereditary papillary renal carcinoma
|