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papillary renal cell carcinoma

Disease Summary
Associated Targets (126)
Tbio

68

Tchem

36

Tclin

17

Tdark

5


GARD Rare
Mondo Description Papillary renal cell carcinoma is a rare subtype of renal cell carcinoma, arising from the renal tubular epithelium and showing a papillary growth pattern, which typically manifests with hematuria, flank pain, palpable abdominal mass or nonspecific symptoms, such as fatigue, weight loss or fever. Symptoms related to metastatic spread, such as bone pain or persistent cough, are frequently associated since early diagnosis is not common. It is typically multifocal, bilateral, and in most cases sporadic, although different hereditary syndromes, such as Hereditary leiomyoma renal cell carcinoma, Birt-Hogg-DubC) syndrome and Tuberous sclerosis, may predispose to the development of papillary renal cell carcinoma.
Uniprot Description A subtype of renal cell carcinoma tending to show a tubulo-papillary architecture formed by numerous, irregular, finger-like projections of connective tissue. Renal cell carcinoma is a heterogeneous group of sporadic or hereditary carcinoma derived from cells of the proximal renal tubular epithelium.
Disease Ontology Description A renal cell carcinoma that is characterized by the development of multiple, bilateral papillary renal tumors.
Mondo Term and Equivalent IDs
MONDO:0017884:  papillary renal cell carcinoma
EFO:0000640: 
GARD:0009572: 
GARD:0009575: 
NCIT:C6975: 
ONCOTREE:PRCC: 
Orphanet:319298: 
Orphanet:47044: 
SCTID:733608000: 
UMLS:C1306837: 
UMLS:C1336078: 
UMLS:CN205129: