Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3318663018 | Hemochromatosis type 3 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3318664012 | Hemochromatosis type 3 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3318665013 | Haemochromatosis type 3 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3318670018 | TFR2 (transferrin receptor 2 gene) related hemochromatosis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3318671019 | TFR2 (transferrin receptor 2 gene) related haemochromatosis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hemochromatosis type 3 | Is a | Hereditary hemochromatosis | true | Inferred relationship | Existential restriction modifier | ||
| Hemochromatosis type 3 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hemochromatosis type 3 | Causative agent | Iron AND/OR iron compound | false | Inferred relationship | Existential restriction modifier | ||
| Hemochromatosis type 3 | Causative agent | Iron and/or iron compound | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR