Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3481834015 | Clear cell papillary renal cell carcinoma (morphologic abnormality) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3481835019 | Clear cell papillary renal cell carcinoma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Clear cell papillary renal cell carcinoma (morphologic abnormality) | Is a | Renal cell carcinoma | false | Inferred relationship | Some | ||
Clear cell papillary renal cell carcinoma (morphologic abnormality) | Is a | Adenomatous neoplasm of borderline malignancy (morphologic abnormality) | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
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. | Associated morphology | True | Clear cell papillary renal cell carcinoma (morphologic abnormality) | Inferred relationship | Some | 1 |
This concept is not in any reference sets