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 |
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