Status: current, Defined. 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 | Case insensitive | SNOMED CT core |
3657945014 | Autosomal dominant polycystic kidney disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
3657946010 | ADPKD - autosomal dominant polycystic kidney disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
3657947018 | Inherited disease with characteristics of the development of cysts in the kidneys. The disease rarely causes any noticeable problems until the cysts grow large enough to affect renal function, usually between 30 and 60 years of age. Less commonly, children or older people may have noticeable symptoms. Two different genes are known to cause this disease PKD1 and PKD2. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant polycystic kidney disease | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant polycystic kidney disease | Finding site | Kidney structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant polycystic kidney disease | Is a | Polycystic kidney disease | true | Inferred relationship | Some | ||
Autosomal dominant polycystic kidney disease | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Autosomal dominant polycystic kidney disease | Associated morphology | Polycystic change | true | Inferred relationship | Some | 1 | |
Autosomal dominant polycystic kidney disease | Is a | Hereditary nephropathy | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Multinodular goitre, cystic kidney, polydactyly syndrome | Is a | True | Autosomal dominant polycystic kidney disease | Inferred relationship | Some | |
Adult type polycystic kidney disease type 2 | Is a | True | Autosomal dominant polycystic kidney disease | Inferred relationship | Some | |
Adult type polycystic kidney disease type 1 | Is a | True | Autosomal dominant polycystic kidney disease | Inferred relationship | Some | |
Autosomal dominant polycystic kidney disease in childhood | Is a | True | Autosomal dominant polycystic kidney disease | Inferred relationship | Some | |
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis | Is a | True | Autosomal dominant polycystic kidney disease | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set