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 |
| 4667830011 | Type 2A juvenile hereditary hemochromatosis (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 4667831010 | Type 2A juvenile hereditary hemochromatosis | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4667832015 | Type 2A juvenile hereditary haemochromatosis | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Type 2A juvenile hereditary hemochromatosis | Is a | Juvenile hemochromatosis | true | Inferred relationship | Existential restriction modifier | ||
| Type 2A juvenile hereditary hemochromatosis | Occurrence | Childhood | true | Inferred relationship | Existential restriction modifier | 1 | |
| Type 2A juvenile hereditary hemochromatosis | Associated morphology | Deposition of iron | true | Inferred relationship | Existential restriction modifier | 1 | |
| Type 2A juvenile hereditary hemochromatosis | 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