Status: current, Primitive. Date: 30-Jun 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5068836018 | FTH1-associated iron overload | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 5068837010 | Ferritin heavy chain 1-related iron overload | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 5068838017 | FTH1-related iron overload | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 5068839013 | FTH1 (ferritin heavy chain 1) related iron overload | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 5068840010 | Ferritin heavy chain 1-related iron overload (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 5068841014 | A rare disorder of iron metabolism and transport characterised by elevated serum ferritin levels, increased serum iron, increased transferrin saturation and heavy iron deposition in hepatocytes. Iron deposition has also been indicated in heart and bone marrow, while haematological examination of peripheral blood shows no abnormalities. | en | Definition | Active | Case sensitive | SNOMED CT core |
| 5068842019 | A rare disorder of iron metabolism and transport characterized by elevated serum ferritin levels, increased serum iron, increased transferrin saturation and heavy iron deposition in hepatocytes. Iron deposition has also been indicated in heart and bone marrow, while hematological examination of peripheral blood shows no abnormalities. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| FTH1-related iron overload | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| FTH1-related iron overload | Is a | Metabolic and genetic disorder affecting the liver | true | Inferred relationship | Some | ||
| FTH1-related iron overload | Is a | Hereditary haemochromatosis | true | Inferred relationship | Some | ||
| FTH1-related iron overload | Is a | Digestive system hereditary disorder | true | Inferred relationship | Some | ||
| FTH1-related iron overload | Finding site | Liver structure | true | Inferred relationship | Some | 1 | |
| FTH1-related iron overload | Causative agent | Iron and/or iron compound | 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