Status: current, Primitive. Date: 30-Nov 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4667830011 | Type 2A juvenile hereditary hemochromatosis (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 4667831010 | Type 2A juvenile hereditary hemochromatosis | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 4667832015 | Type 2A juvenile hereditary haemochromatosis | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Type 2A juvenile hereditary haemochromatosis | Is a | Juvenile haemochromatosis | true | Inferred relationship | Some | ||
| Type 2A juvenile hereditary haemochromatosis | Occurrence | Childhood | true | Inferred relationship | Some | 1 | |
| Type 2A juvenile hereditary haemochromatosis | Associated morphology | Deposition of iron | true | Inferred relationship | Some | 1 | |
| Type 2A juvenile hereditary haemochromatosis | Causative agent | Iron and/or iron compound | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR