Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2009. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2789394016 | Hereditary factor XIII A subunit deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 2791451014 | Hereditary factor XIII A subunit deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 2791452019 | Hereditary factor XIII type II deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 2794617018 | Hereditary factor XIII alpha subunit deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary factor XIII A subunit deficiency | Is a | Hereditary factor XIII deficiency disease | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary factor XIII A subunit deficiency | Interprets | Hemostatic function | true | Inferred relationship | Existential restriction modifier | 1 | |
| Hereditary factor XIII A subunit deficiency | Has interpretation | Abnormal | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR