Status: current, Sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4591510019 | Hereditary congenital prekallikrein deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4591511015 | Hereditary congenital prekallikrein deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4591518014 | Congenital Fletcher factor deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary congenital prekallikrein deficiency | Is a | Prekallikrein deficiency | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary congenital prekallikrein deficiency | Is a | Congenital disease | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary congenital prekallikrein deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary congenital prekallikrein deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 | |
| Hereditary congenital prekallikrein deficiency | Interprets | Hemostatic function | true | Inferred relationship | Existential restriction modifier | 1 | |
| Hereditary congenital prekallikrein 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