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 |
| 43600019 | Mild hemophilia A | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 43601015 | 6-60% of normal factor VIII | en | Synonym (core metadata concept) | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 483093012 | Mild haemophilia A | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 756414016 | Mild hemophilia A (disorder) | en | Fully specified name | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2787929017 | Mild hereditary factor VIII deficiency disease (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2792392016 | Mild hereditary factor VIII deficiency disease | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2884517012 | Mild disease manifests factor VIII activity of greater than 5% of normal | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5449358013 | A mild form of haemophilia A characterised by a small deficiency of factor VIII (biological activity between 5 and 40 IU/dL) leading to abnormal bleeding as a result of minor injuries or following surgery or tooth extraction. Spontaneous haemorrhages do not occur. Patients may be also labelled as having mild haemophilia A if they have a FVIII >40 IU/dL and a DNA change in the F8 gene and one of the following: (i) a family member with the same DNA change and FVIII of <40 IU/dL, and the DNA change is found in <1% of the population; and (ii) the international databases list the DNA change as being associated with haemophilia A and <40 IU/dL FVIII. The condition may affect males and female carriers of disease-causing mutations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5449359017 | A mild form of hemophilia A characterized by a small deficiency of factor VIII (biological activity between 5 and 40 IU/dL) leading to abnormal bleeding as a result of minor injuries or following surgery or tooth extraction. Spontaneous hemorrhages do not occur. Patients may be also labeled as having mild hemophilia A if they have a FVIII >40 IU/dL and a DNA change in the F8 gene and one of the following: (i) a family member with the same DNA change and FVIII of <40 IU/dL, and the DNA change is found in <1% of the population; and (ii) the international databases list the DNA change as being associated with hemophilia A and <40 IU/dL FVIII. The condition may affect males and 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 |
| Mild hereditary factor VIII deficiency disease (disorder) | Is a | Hereditary factor VIII deficiency disease | true | Inferred relationship | Some | ||
| Mild hereditary factor VIII deficiency disease (disorder) | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| Mild hereditary factor VIII deficiency disease (disorder) | Severity | Mild | false | Inferred relationship | Some | ||
| Mild hereditary factor VIII deficiency disease (disorder) | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Mild hereditary factor VIII deficiency disease (disorder) | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| Mild hereditary factor VIII deficiency disease (disorder) | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
| Mild hereditary factor VIII deficiency disease (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Mild hereditary factor VIII deficiency disease with inhibitor (disorder) | Is a | True | Mild hereditary factor VIII deficiency disease (disorder) | Inferred relationship | Some |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR