Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Nov 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4668225019 | Haemochromatosis type 1 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4668226018 | Hemochromatosis type 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4668227010 | Hemochromatosis type 1 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4668470013 | HFE related haemochromatosis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 4668471012 | HFE related hemochromatosis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hemochromatosis type 1 | Causative agent | Iron and/or iron compound | true | Inferred relationship | Existential restriction modifier | 1 | |
| Hemochromatosis type 1 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hemochromatosis type 1 | Is a | Hereditary hemochromatosis | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Symptomatic form of hemochromatosis type 1 | Is a | True | Hemochromatosis type 1 | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR