Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5408830019 | A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5408831015 | A primary glomerular disease characterised by proteinuria, type IV renal tubular acidosis, microscopic haematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3856295011 | Fibronectin glomerulopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3856296012 | Glomerulopathy with fibronectin deposits | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3856297015 | Fibronectin glomerulopathy (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 |
| A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. | Is a | Autosomal dominant hereditary disorder (disorder) | true | Inferred relationship | Some | ||
| A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. | Is a | Hereditary nephropathy (disorder) | true | Inferred relationship | Some | ||
| A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. | Is a | Renal disorders in inherited disease | false | Inferred relationship | Some | ||
| A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. | Is a | Glomerular disease | true | Inferred relationship | Some | ||
| A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. | Finding site | Glomerulus structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Glomerulopathy with giant fibrillar deposits (disorder) | Is a | True | A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. | Inferred relationship | Some | |
| Glomerulopathy with fibronectin deposits 2 (disorder) | Is a | True | A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. | Inferred relationship | Some |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)