Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
68137016 | Hereditary factor VII deficiency syndrome | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
68138014 | Hereditary hypoproconvertinemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
492809012 | Hereditary hypoproconvertinaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
2789802015 | Hereditary factor VII deficiency disease (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
2794698010 | Hereditary factor VII deficiency disease | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets