Preferred Name | papillary renal cell carcinoma | |
Synonyms |
papillary renal cell carcinoma, familial - (subtype) papillary renal carcinoma, malignant - (subtype) RCCP1 RCCP renal adenocarcinoma papillary renal cell carcinoma, sporadic - (subtype) renal cell carcinoma, papillary, 1 chromophil RCC papillary renal cell carcinoma, multiple - (subtype) papillary renal cell carcinoma, bilateral - (subtype) papillary renal cell adenocarcinoma HPRCC papillary renal cell cancer papillary (chromophil) renal cell carcinoma renal cell carcinoma, papillary, type 1 papillary kidney carcinoma chromophil carcinoma of kidney chromophil renal cell carcinoma sporadic papillary renal cell carcinoma chromophil carcinoma of the kidney papillary renal cell carcinoma |
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Definitions |
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. |
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ID |
http://purl.obolibrary.org/obo/MONDO_0017884 |
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closeMatch |
http://identifiers.org/snomedct/4797003 |
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database_cross_reference |
ONCOTREE:PRCC Orphanet:319298 GARD:0009575 EFO:0000640 UMLS:C1336078 DOID:4465 UMLS:CN205129 UMLS:C1306837 GARD:0009572 NCIT:C6975 SCTID:733608000 ICD10:C64 OMIM:605074 Orphanet:47044 |
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exactMatch |
http://purl.obolibrary.org/obo/NCIT_C6975 http://www.orpha.net/ORDO/Orphanet_319298 http://linkedlifedata.com/resource/umls/id/C2931899 http://identifiers.org/omim/605074 http://identifiers.org/mesh/C538614 http://linkedlifedata.com/resource/umls/id/C1306837 http://linkedlifedata.com/resource/umls/id/CN205129 http://identifiers.org/snomedct/733608000 http://purl.obolibrary.org/obo/DOID_4465 |
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excluded from QC check |
http://purl.obolibrary.org/obo/mondo/sparql/single-child-tags.sparql |
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has exact synonym |
papillary renal cell adenocarcinoma HPRCC papillary renal cell cancer papillary (chromophil) renal cell carcinoma renal cell carcinoma, papillary, type 1 papillary kidney carcinoma chromophil carcinoma of kidney chromophil renal cell carcinoma sporadic papillary renal cell carcinoma chromophil carcinoma of the kidney papillary renal cell carcinoma |
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has related synonym |
papillary renal cell carcinoma, familial - (subtype) papillary renal carcinoma, malignant - (subtype) RCCP1 RCCP renal adenocarcinoma papillary renal cell carcinoma, sporadic - (subtype) renal cell carcinoma, papillary, 1 chromophil RCC papillary renal cell carcinoma, multiple - (subtype) papillary renal cell carcinoma, bilateral - (subtype) |
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id |
MONDO:0017884 |
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imported from | ||
in_subset | ||
label |
papillary renal cell carcinoma |
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notation |
MONDO:0017884 |
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prefLabel |
papillary renal cell carcinoma |
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see also |
https://rarediseases.info.nih.gov/diseases/9572/papillary-renal-cell-carcinoma |
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textual 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. |
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excluded subClassOf | ||
subClassOf |