Status: current, Defined. Date: 30-Apr 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2788435014 | Hereditary heparin cofactor II deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 2794143018 | Hereditary heparin cofactor II deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary heparin cofactor II deficiency | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Hereditary heparin cofactor II deficiency | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Hereditary heparin cofactor II deficiency | Is a | Hereditary thrombophilia | true | Inferred relationship | Some | ||
| Hereditary heparin cofactor II deficiency | Is a | Heparin cofactor II deficiency | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR