Status: current, Not 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 |
| 5170842015 | De novo thrombotic microangiopathy after kidney transplantation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5170843013 | De novo thrombotic microangiopathy following transplant of kidney (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5170844019 | De novo thrombotic microangiopathy following transplant of kidney | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5170851011 | De novo thrombotic microangiopathy after renal transplant | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5170849012 | A rare renal disease characterized by thrombotic microangiopathy developing de novo in kidney transplant recipients with no evidence of occurrence of the disease prior to transplantation. Precipitating factors include antibody-mediated rejection, immunosuppressive medication, viral infections and genetic abnormalities in the complement cascade, among others. The condition most commonly occurs within the first 3-6 months post-transplantation. Clinical presentation is highly variable and ranges from a limited form confined to the kidney with relatively good prognosis to a systemic variant consisting of the classic triad of thrombocytopenia, microangiopathic hemolytic anemia and acute kidney injury. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5170850012 | A rare renal disease characterised by thrombotic microangiopathy developing de novo in kidney transplant recipients with no evidence of occurrence of the disease prior to transplantation. Precipitating factors include antibody-mediated rejection, immunosuppressive medication, viral infections and genetic abnormalities in the complement cascade, among others. The condition most commonly occurs within the first 3-6 months post-transplantation. Clinical presentation is highly variable and ranges from a limited form confined to the kidney with relatively good prognosis to a systemic variant consisting of the classic triad of thrombocytopenia, microangiopathic haemolytic anaemia and acute kidney injury. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| De novo thrombotic microangiopathy following transplant of kidney (disorder) | Is a | Thrombotic microangiopathy (disorder) | true | Inferred relationship | Some | ||
| De novo thrombotic microangiopathy following transplant of kidney (disorder) | Is a | Postoperative complication (disorder) | true | Inferred relationship | Some | ||
| De novo thrombotic microangiopathy following transplant of kidney (disorder) | Is a | Disorder related to renal transplantation (disorder) | true | Inferred relationship | Some | ||
| De novo thrombotic microangiopathy following transplant of kidney (disorder) | Is a | Arterial complication of procedure | true | Inferred relationship | Some | ||
| De novo thrombotic microangiopathy following transplant of kidney (disorder) | After | Transplant of kidney | true | Inferred relationship | Some | 3 | |
| De novo thrombotic microangiopathy following transplant of kidney (disorder) | Finding site | Structure of capillary blood vessel | true | Inferred relationship | Some | 1 | |
| De novo thrombotic microangiopathy following transplant of kidney (disorder) | Associated morphology | Microthrombus (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| De novo thrombotic microangiopathy following transplant of kidney (disorder) | Finding site | Structure of arteriole | true | Inferred relationship | Some | 2 | |
| De novo thrombotic microangiopathy following transplant of kidney (disorder) | Associated morphology | Microthrombus (morphologic abnormality) | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR