Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5180538019 | Hereditary primary clear cell renal cell carcinoma (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5180539010 | Hereditary primary clear cell renal cell carcinoma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5180540012 | Hereditary primary clear cell renal cell adenocarcinoma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 6477711000146119 | hereditair 'clear cell'-niercelcarcinoom (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6477721000146112 | erfelijk heldercellig nierceladenocarcinoom | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6477731000146114 | hereditair 'clear cell'-niercelcarcinoom | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3657276012 | A hereditary renal cancer syndrome defined as development of hereditary clear cell renal cell carcinoma (ccRCC) in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other neoplasm predisposing syndromes associated with ccRCC, such as tuberous sclerosis or Birt-Hogg-Dubbe syndrome. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary primary clear cell renal cell carcinoma (disorder) | Is a | Familial neoplastic disease | false | Inferred relationship | Some | ||
| Hereditary primary clear cell renal cell carcinoma (disorder) | Is a | Clear cell carcinoma of kidney | false | Inferred relationship | Some | ||
| Hereditary primary clear cell renal cell carcinoma (disorder) | Is a | Hereditary cancer-predisposing syndrome | false | Inferred relationship | Some | ||
| Hereditary primary clear cell renal cell carcinoma (disorder) | Is a | Hereditary nephropathy (disorder) | false | Inferred relationship | Some | ||
| Hereditary primary clear cell renal cell carcinoma (disorder) | Associated morphology | Clear cell adenocarcinoma | false | Inferred relationship | Some | 1 | |
| Hereditary primary clear cell renal cell carcinoma (disorder) | Finding site | Structure of parenchyma of kidney | true | Inferred relationship | Some | 1 | |
| Hereditary primary clear cell renal cell carcinoma (disorder) | Is a | Familial renal cell carcinoma (disorder) | true | Inferred relationship | Some | ||
| Hereditary primary clear cell renal cell carcinoma (disorder) | Associated morphology | Clear cell renal cell carcinoma | true | Inferred relationship | Some | 1 | |
| Hereditary primary clear cell renal cell carcinoma (disorder) | Is a | Primary clear cell carcinoma of kidney | true | Inferred relationship | Some | ||
| Hereditary primary clear cell renal cell carcinoma (disorder) | Pathological process (attribute) | Malignant proliferation of primary neoplasm (qualifier value) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Dutch pathology simple reference set (foundation metadata concept)
FHIR