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 |
| 127274011 | Factor X deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 127275012 | Factor X deficiency, NOS | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 817385017 | Factor X deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 1234012018 | Stuart-Prower factor deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3036019012 | Factor 10 deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Factor X deficiency | Is a | Prothrombin complex deficiency | true | Inferred relationship | Existential restriction modifier | ||
| Factor X deficiency | Is a | Coagulation factor deficiency syndrome | true | Inferred relationship | Existential restriction modifier | ||
| Factor X deficiency | Finding site | Entire hematological system | false | Inferred relationship | Existential restriction modifier | ||
| Factor X deficiency | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Factor X deficiency | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Existential restriction modifier | ||
| Factor X deficiency | Interprets | Hemostatic function | true | Inferred relationship | Existential restriction modifier | 1 | |
| Factor X deficiency | Has interpretation | Abnormal | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Acquired factor X deficiency disease | Is a | True | Factor X deficiency | Inferred relationship | Existential restriction modifier | |
| Hereditary factor X deficiency disease | Is a | True | Factor X deficiency | Inferred relationship | Existential restriction modifier | |
| Deficiency of factor X due to systemic amyloidosis | Is a | True | Factor X deficiency | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR