Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1771187018 | Skin pigmentation due to hemosiderosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 1773704013 | Skin pigmentation due to haemosiderosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 1774990012 | Skin pigmentation due to hemosiderosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 1783785018 | Cutaneous haemosiderosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 1784171012 | Cutaneous hemosiderosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Skin pigmentation due to haemosiderosis | Is a | Endogenous non-melanin pigmentation | true | Inferred relationship | Some | ||
| Skin pigmentation due to haemosiderosis | Finding site | Skin structure | true | Inferred relationship | Some | 2 | |
| Skin pigmentation due to haemosiderosis | Due to | Haemosiderosis | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Haemosiderin pigmentation of skin due to venous insufficiency | Is a | False | Skin pigmentation due to haemosiderosis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR