Status: current, Defined. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2994983013 | Hereditary hyperferritinemia-cataract syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
2995014019 | Hyperferritinemia cataract syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
2995493017 | Hyperferritinemia cataract syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
2995902012 | Bonneau-Beaumont syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hyperferritinemia cataract syndrome | Finding site | Structure of lens of eye | true | Inferred relationship | Some | 1 | |
Hyperferritinemia cataract syndrome | Associated morphology | Abnormally opaque structure | true | Inferred relationship | Some | 1 | |
Hyperferritinemia cataract syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Hyperferritinemia cataract syndrome | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Some | ||
Hyperferritinemia cataract syndrome | Is a | Cataract | true | Inferred relationship | Some | ||
Hyperferritinemia cataract syndrome | Associated with | Serum ferritin above reference range | true | Inferred relationship | Some | 2 | |
Hyperferritinemia cataract syndrome | Associated morphology | Cataract | false | Inferred relationship | Some | 2 | |
Hyperferritinemia cataract syndrome | Finding site | Structure of lens of eye | false | 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