Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3306956019 | Alport syndrome autosomal dominant (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
3310200014 | Alport syndrome autosomal dominant | en | Synonym | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Alport syndrome autosomal dominant | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Alport syndrome autosomal dominant | Is a | Hereditary nephritis | false | Inferred relationship | Some | ||
Alport syndrome autosomal dominant | Associated morphology | Chronic inflammation | true | Inferred relationship | Some | 1 | |
Alport syndrome autosomal dominant | Finding site | Glomerulus structure | true | Inferred relationship | Some | 1 | |
Alport syndrome autosomal dominant | Interprets | Hearing | true | Inferred relationship | Some | 2 | |
Alport syndrome autosomal dominant | Is a | Alport syndrome | true | Inferred relationship | Some | ||
Alport syndrome autosomal dominant | Finding site | Structure of auditory system | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set