Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3756649011 | Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3756650011 | Haemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3756651010 | Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3756652015 | A rare genetic constitutional coagulation factor defect disorder characterized by a bleeding tendency of variable severity due to methionine 358 to arginine replacement (Pittsburgh mutation) in the alpha-1-antitrypsin protein. Patients present with spontaneous hematomas, hematomas following minor trauma or surgery and in female patients ovarian hematomas after ovulation. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3756653013 | A rare genetic constitutional coagulation factor defect disorder characterised by a bleeding tendency of variable severity due to methionine 358 to arginine replacement (Pittsburgh mutation) in the alpha-1-antitrypsin protein. Patients present with spontaneous haematomas, haematomas following minor trauma or surgery and in female patients ovarian haematomas after ovulation. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation | Is a | Blood coagulation disorder | true | Inferred relationship | Some | ||
| Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
| Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR