Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5179263019 | Primary clear cell carcinoma of kidney | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5179264013 | Primary clear cell carcinoma of kidney (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Primary clear cell carcinoma of kidney | Is a | Primary renal cell carcinoma (disorder) | true | Inferred relationship | Some | ||
Primary clear cell carcinoma of kidney | Is a | Clear cell carcinoma of kidney | true | Inferred relationship | Some | ||
Primary clear cell carcinoma of kidney | Finding site | Structure of parenchyma of kidney | true | Inferred relationship | Some | 1 | |
Primary clear cell carcinoma of kidney | Associated morphology | Clear cell renal cell carcinoma | true | Inferred relationship | Some | 1 | |
Primary clear cell carcinoma of kidney | Pathological process (attribute) | Malignant proliferation of primary neoplasm (qualifier value) | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Hereditary clear cell renal cell carcinoma (ccRCC) is a hereditary renal cancer syndrome defined as development of ccRCC in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other tumor predisposing syndromes associated with ccRCC, such as tuberous sclerosis or Birt-Hogg-Dubé syndrome. | Is a | True | Primary clear cell carcinoma of kidney | Inferred relationship | Some |
This concept is not in any reference sets