Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 28565012 | Severe hemophilia A | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 28566013 | Less than 1% of normal factor VIII | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 477973011 | Severe haemophilia A | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 743981012 | Severe hemophilia A (disorder) | en | Fully specified name | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2788401011 | Severe hereditary factor VIII deficiency disease (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2795425017 | Severe hereditary factor VIII deficiency disease | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2884791011 | Severe disease manifests factor VIII activity of less than 1%, except in the U.K. and Italy, where severe disease includes factor VIII activity levels of less than 2% | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5447279016 | A severe form of hemophilia A characterized by a large deficiency of factor VIII (biological activity <1 IU/dL) leading to frequent spontaneous hemorrhage and abnormal bleeding as a result of minor injuries, or following trauma, surgery or tooth extraction. It primarily affects males but may also be observed in female carriers of disease-causing mutations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5447280018 | A severe form of haemophilia A characterised by a large deficiency of factor VIII (biological activity <1 IU/dL) leading to frequent spontaneous haemorrhage and abnormal bleeding as a result of minor injuries, or following trauma, surgery or tooth extraction. It primarily affects males but may also be observed in female carriers of disease-causing mutations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Severe hereditary factor VIII deficiency disease (disorder) | Is a | Hereditary factor VIII deficiency disease | true | Inferred relationship | Some | ||
| Severe hereditary factor VIII deficiency disease (disorder) | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| Severe hereditary factor VIII deficiency disease (disorder) | Severity | Severe | false | Inferred relationship | Some | ||
| Severe hereditary factor VIII deficiency disease (disorder) | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Severe hereditary factor VIII deficiency disease (disorder) | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| Severe hereditary factor VIII deficiency disease (disorder) | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
| Severe hereditary factor VIII deficiency disease (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Severe hereditary factor VIII deficiency disease with inhibitor (disorder) | Is a | True | Severe hereditary factor VIII deficiency disease (disorder) | Inferred relationship | Some |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR