Status: current. Date: 30-Jun 2022
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5068836018 | FTH1-associated iron overload | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5068837010 | Ferritin heavy chain 1-related iron overload | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5068838017 | FTH1-related iron overload | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5068839013 | FTH1 (ferritin heavy chain 1) related iron overload | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5068840010 | Ferritin heavy chain 1-related iron overload (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | 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 | Inactive | Entire term case sensitive (core metadata concept) | 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 | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400145011 | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400146012 | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| FTH1-related iron overload | Is a | Autosomal dominant hereditary disorder | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| FTH1-related iron overload | Is a | Hereditary metabolic disease | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| FTH1-related iron overload | Is a | Metabolic and genetic disorder affecting the liver | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| FTH1-related iron overload | Is a | Hemochromatosis (disorder) | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| FTH1-related iron overload | Causative agent | Iron and/or iron compound | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 | |
| FTH1-related iron overload | Finding site | Liver structure | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR