Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3310202018 | Alport syndrome autosomal recessive (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3312046012 | Alport syndrome autosomal recessive | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Alport syndrome autosomal recessive | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Alport syndrome autosomal recessive | Is a | Hereditary nephritis | false | Inferred relationship | Some | ||
Alport syndrome autosomal recessive | Associated morphology | Chronic inflammation | true | Inferred relationship | Some | 1 | |
Alport syndrome autosomal recessive | Finding site | Glomerulus structure | true | Inferred relationship | Some | 1 | |
Alport syndrome autosomal recessive | Finding site | Structure of auditory system | true | Inferred relationship | Some | 3 | |
Alport syndrome autosomal recessive | Is a | Alport syndrome | true | Inferred relationship | Some | ||
Alport syndrome autosomal recessive | Interprets | Hearing | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Unit of use quantity reference set
Description inactivation indicator reference set