Status: retired, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 143918018 | Hemochromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 143919014 | Hemochromatosis, NOS | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 143920015 | Iron storage disease, NOS | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 143921016 | Bronzed cirrhosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 143922011 | Pigmentary cirrhosis of liver | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 143923018 | von Recklinghausen-Appelbaum disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 143924012 | Iron storage disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 507253013 | Familial hemochromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 507254019 | Hereditary hemochromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 507255018 | Primary hemochromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 507256017 | Idiopathic hemochromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 507257014 | Familial haemochromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 507258016 | Hereditary haemochromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 507259012 | Idiopathic haemochromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 507260019 | Primary haemochromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 507261015 | Bronzed diabetes | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 507262010 | von Recklinghausen-Applebaum disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 507263017 | Haemochromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 829117016 | Hemochromatosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Haemochromatosis | Is a | Iron overload | false | Inferred relationship | Some | ||
| Haemochromatosis | Is a | Metabolic and genetic disorder affecting the liver | false | Inferred relationship | Some | ||
| Haemochromatosis | Finding site | Liver structure | false | Inferred relationship | Some | ||
| Haemochromatosis | Causative agent | Iron | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary haemochromatosis | Is a | False | Haemochromatosis | Inferred relationship | Some | |
| Juvenile haemochromatosis | Is a | False | Haemochromatosis | Inferred relationship | Some | |
| Secondary haemochromatosis | Is a | False | Haemochromatosis | Inferred relationship | Some | |
| Restrictive cardiomyopathy secondary to haemochromatosis | Is a | False | Haemochromatosis | Inferred relationship | Some | |
| Neonatal haemochromatosis | Is a | False | Haemochromatosis | Inferred relationship | Some | |
| Dilated cardiomyopathy due to haemochromatosis | Is a | False | Haemochromatosis | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set
SAME AS association reference set