Status: current, Sufficiently defined by necessary conditions definition status. Date: 30-Apr 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2788412011 | Hereditary protein C deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 2791269015 | Hereditary protein C deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary protein C deficiency | Is a | Protein C deficiency disease | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary protein C deficiency | Is a | Hereditary thrombophilia | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary protein C deficiency | Interprets | Hemostatic function | true | Inferred relationship | Existential restriction modifier | 1 | |
| Hereditary protein C deficiency | Has interpretation | Abnormal | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Heterozygous protein C deficiency | Is a | True | Hereditary protein C deficiency | Inferred relationship | Existential restriction modifier | |
| Homozygous protein C deficiency | Is a | True | Hereditary protein C deficiency | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR