Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2994983013 | Hereditary hyperferritinemia-cataract syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 2995014019 | Hyperferritinemia cataract syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 2995493017 | Hyperferritinemia cataract syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 2995902012 | Bonneau-Beaumont syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets