Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1781593012 | Primary systemic amyloidosis associated with occult plasma cell dyscrasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3874053014 | Primary systemic amyloidosis due to occult plasma cell dyscrasia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3874054015 | Primary systemic amyloidosis due to occult plasma cell dyscrasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Is a | AL amyloidosis | true | Inferred relationship | Some | ||
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Interprets | Immunoglobulin measurement | true | Inferred relationship | Some | 1 | |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Has interpretation | Above reference range | true | Inferred relationship | Some | 1 | |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Has interpretation | Present | true | Inferred relationship | Some | 3 | |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Interprets | Paraprotein measurement | true | Inferred relationship | Some | 3 | |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Associated morphology | Amyloid deposition | true | Inferred relationship | Some | 4 | |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Causative agent | Immunoglobulin, light chain | true | Inferred relationship | Some | 4 | |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Has interpretation | Above reference range | true | Inferred relationship | Some | 5 | |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Interprets | Serum globulin measurement | true | Inferred relationship | Some | 5 | |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 6 | |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Is a | Primary systemic (AL fibril type) amyloidosis | false | Inferred relationship | Some | ||
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Associated morphology | Amyloid deposition | false | Inferred relationship | Some | ||
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Associated morphology | Focal amyloid | false | Inferred relationship | Some | 1 | |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Due to | Plasma cell neoplasm | true | Inferred relationship | Some | 2 | |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Associated morphology | Focal amyloid | false | Inferred relationship | Some | 2 | |
Primary systemic amyloidosis due to occult plasma cell dyscrasia | Finding site | Skin structure | 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
Description inactivation indicator reference set