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. [ Orphanet:319298 ]

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:0009572 (MONDO:equivalentTo)
  • ICD10:C64 (Orphanet:47044)
  • NCIT:C6975 (MONDO:equivalentTo)
  • ONCOTREE:PRCC (MONDO:equivalentTo)
  • SCTID:733608000 (MONDO:equivalentTo)
  • UMLS:CN205129 (MONDO:equivalentTo)
  • UMLS:C1306837 (Orphanet:319298)
  • DOID:4465 (MONDO:equivalentTo)
  • EFO:0000640 (MONDO:equivalentTo)
  • Orphanet:47044 (OMIM:605074)
  • GARD:0009575 (shared-umls-xref)
  • OMIM:605074 (Orphanet:47044)
  • UMLS:C1336078 (MONDO:equivalentTo)
  • Orphanet:319298 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease

abbreviation
HPRCC [ Orphanet:47044 ]

abbreviation
RCCP [ GARD:0009572 ]

closeMatch

http://identifiers.org/snomedct/4797003

http://linkedlifedata.com/resource/umls/id/C1336839

http://purl.obolibrary.org/obo/NCIT_C27890

definition

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.

exactMatch

http://purl.obolibrary.org/obo/NCIT_C6975

http://purl.obolibrary.org/obo/DOID_4465

http://identifiers.org/mesh/C538614

http://linkedlifedata.com/resource/umls/id/C2931899

http://linkedlifedata.com/resource/umls/id/CN205129

http://www.orpha.net/ORDO/Orphanet_319298

http://linkedlifedata.com/resource/umls/id/C1336078

http://linkedlifedata.com/resource/umls/id/C1306837

http://identifiers.org/snomedct/733608000

http://www.orpha.net/ORDO/Orphanet_47044

http://identifiers.org/omim/605074

excluded from QC check

http://purl.obolibrary.org/obo/mondo/sparql/single-child-tags.sparql

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0017891

has exact synonym

renal cell carcinoma, papillary, type 1

chromophil renal cell carcinoma

papillary (chromophil) renal cell carcinoma

papillary renal cell carcinoma

sporadic papillary renal cell carcinoma

papillary kidney carcinoma

chromophil carcinoma of kidney

chromophil carcinoma of the kidney

HPRCC

papillary renal cell adenocarcinoma

papillary renal cell cancer

has related synonym

RCCP1

chromophil RCC

papillary renal cell carcinoma, bilateral - (subtype)

renal adenocarcinoma

papillary renal cell carcinoma, multiple - (subtype)

RCCP

papillary renal carcinoma, malignant - (subtype)

renal cell carcinoma, papillary, 1

papillary renal cell carcinoma, sporadic - (subtype)

papillary renal cell carcinoma, familial - (subtype)

id

MONDO:0017884

seeAlso

https://rarediseases.info.nih.gov/diseases/9572/papillary-renal-cell-carcinoma