Status: current, Primitive. Date: 30-Jun 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5071671014 | AH amyloidosis (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| 5071672019 | AH amyloidosis | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 5071673012 | Heavy chain amyloidosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 5071674018 | A rare systemic amyloidosis with characteristics of the aggregation and deposition of amyloid fibrils composed of monoclonal immunoglobulin heavy-chain fragments, usually produced by a plasma cell neoplasm. Amyloid fibrils deposit in various organs, most commonly in the kidneys. It typically affects older patients and clinical presentation includes signs and symptoms of renal dysfunction, sometimes leading to nephrotic syndrome and end stage renal disease. Cardiac, liver and nerve involvement has also been described. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| AH amyloidosis | Is a | Systemic amyloidosis | true | Inferred relationship | Some | ||
| AH amyloidosis | Associated morphology | Amyloid deposition | true | Inferred relationship | Some | 1 | |
| AH amyloidosis | Causative agent | Immunoglobulin heavy chain | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR