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 | 
| 62309012 | Hereditary factor X deficiency disease | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module | 
| 62310019 | Hereditary Stuart factor deficiency disease | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module | 
| 62311015 | Hereditary Stuart-Prower deficiency disease | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module | 
| 769207019 | Hereditary factor X deficiency disease (disorder) | en | Fully specified name | 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