Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hypernephroma |
Is a |
False |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Metastatic renal cell carcinoma |
Is a |
False |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Renal cell carcinoma of kidney except renal pelvis (disorder) |
Is a |
True |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Tubulocystic renal cell carcinoma (disorder) |
Is a |
True |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Papillary renal cell carcinoma (disorder) |
Is a |
True |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Clear cell papillary renal cell carcinoma is a rare, indolent subtype of clear cell renal carcinoma, arising from epithelial cells in the renal cortex. It most frequently manifests with a well-circumscribed, well-encapsulated, unicentric, unilateral, small tumour that typically does not metastasize. Clinically it can present with flank or abdominal pain or haematuria, although most patients are usually asymptomatic at the time of diagnosis. Bilateral and/or multifocal presentation should raise the suspicion of von Hippel-Lindau syndrome. |
Is a |
False |
Renal cell carcinoma |
Inferred relationship |
Some |
|
MiT family translocation renal cell carcinoma |
Is a |
True |
Renal cell carcinoma |
Inferred relationship |
Some |
|
A rare subtype of renal cell carcinoma, occurring in the context of end-stage kidney disease and acquired cystic kidney disease, characterized by a usually well circumscribed, solid, multifocal, bilateral tumor with inter- or intracellular microlumen formation (leading to cribiform architecture). Tumors are often diagnosed incidentally in early stages, although complications caused by renal cysts (dull flank or abdominal pain, fever) or renal parenchymal bleeding may mask the underlying neoplastic process. Most have an indolent behavior. |
Is a |
True |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Familial renal cell carcinoma (disorder) |
Is a |
True |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Mucinous tubular and spindle cell renal carcinoma |
Is a |
True |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Renal medullary carcinoma |
Is a |
True |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Chromophobe renal cell carcinoma |
Is a |
True |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Cystic renal cell carcinoma of kidney |
Is a |
True |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Primary renal cell carcinoma of left kidney |
Is a |
False |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Primary renal cell carcinoma of right kidney |
Is a |
False |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Clear cell carcinoma of kidney |
Is a |
True |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Removal of tumor thrombus associated with renal cell carcinoma from inferior vena cava by open approach (procedure) |
Has focus |
True |
Renal cell carcinoma |
Inferred relationship |
Some |
2 |
Primary renal cell carcinoma (disorder) |
Is a |
True |
Renal cell carcinoma |
Inferred relationship |
Some |
|
Metastatic renal cell carcinoma to kidney |
Is a |
False |
Renal cell carcinoma |
Inferred relationship |
Some |
|