Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3657944013 | Autosomal dominant polycystic kidney disease (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3657945014 | Autosomal dominant polycystic kidney disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3657946010 | ADPKD - autosomal dominant polycystic kidney disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5404533019 | A rare, genetic, renal tubular disease characterized by progressive outgrowths of fluid-filled cysts from the renal epithelium, which can manifest with hematuria, urinary tract infections, hypertension, and abdominal or flank pain. The slowly progressive loss of kidney function may evolve to end stage kidney disease (ESKD). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5404534013 | A rare, genetic, renal tubular disease characterised by progressive outgrowths of fluid-filled cysts from the renal epithelium, which can manifest with haematuria, urinary tract infections, hypertension, and abdominal or flank pain. The slowly progressive loss of kidney function may evolve to end stage kidney disease (ESKD). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant polycystic kidney disease (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Autosomal dominant polycystic kidney disease (disorder) | Finding site | Kidney structure | true | Inferred relationship | Some | 1 | |
| Autosomal dominant polycystic kidney disease (disorder) | Is a | Congenital cystic kidney disease | true | Inferred relationship | Some | ||
| Autosomal dominant polycystic kidney disease (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Autosomal dominant polycystic kidney disease (disorder) | Associated morphology | Polycystic change | true | Inferred relationship | Some | 1 | |
| Autosomal dominant polycystic kidney disease (disorder) | Is a | Hereditary nephropathy (disorder) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Adult type polycystic kidney disease type 2 (disorder) | Is a | True | Autosomal dominant polycystic kidney disease (disorder) | Inferred relationship | Some | |
| Adult type polycystic kidney disease type 1 (disorder) | Is a | True | Autosomal dominant polycystic kidney disease (disorder) | Inferred relationship | Some | |
| Autosomal dominant polycystic kidney disease in childhood | Is a | True | Autosomal dominant polycystic kidney disease (disorder) | Inferred relationship | Some | |
| Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (disorder) | Is a | True | Autosomal dominant polycystic kidney disease (disorder) | Inferred relationship | Some | |
| Multinodular goiter, cystic kidney, polydactyly syndrome (disorder) | Is a | True | Autosomal dominant polycystic kidney disease (disorder) | Inferred relationship | Some |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR