Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 146804016 | Factor XI deficiency, type I | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 831245011 | Factor XI deficiency, type I (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Factor XI deficiency, type I | Is a | Hereditary factor XI deficiency disease | true | Inferred relationship | Existential restriction modifier | ||
| Factor XI deficiency, type I | Finding site | Entire hematological system | false | Inferred relationship | Existential restriction modifier | ||
| Factor XI deficiency, type I | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Factor XI deficiency, type I | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Existential restriction modifier | ||
| Factor XI deficiency, type I | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 | |
| Factor XI deficiency, type I | Interprets | Hemostatic function | true | Inferred relationship | Existential restriction modifier | 1 | |
| Factor XI deficiency, type I | 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