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 |
| 2790023015 | Severe hereditary factor IX deficiency disease with inhibitor (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 2792952010 | Severe hemophilia B with inhibitor | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 2792953017 | Severe hereditary factor IX deficiency disease with inhibitor | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 2794297013 | Severe haemophilia B with inhibitor | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Severe hereditary factor IX deficiency disease with inhibitor | Is a | Hereditary factor IX deficiency disease with inhibitor | true | Inferred relationship | Existential restriction modifier | ||
| Severe hereditary factor IX deficiency disease with inhibitor | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 | |
| Severe hereditary factor IX deficiency disease with inhibitor | Interprets | Hemostatic function | true | Inferred relationship | Existential restriction modifier | 1 | |
| Severe hereditary factor IX deficiency disease with inhibitor | 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