Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3660331010 | Bleeding disorder due to glycoprotein VI deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3660332015 | Bleeding disorder due to glycoprotein VI deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3660333013 | Glycoprotein VI deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3660335018 | Bleeding disorder platelet-type 11 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3660334019 | A bleeding disorder associated with a decreased ability to form blood clots resulting in increased risk of epistaxis, heavy or prolonged bleeding following minor injury or surgery, ecchymosis and menorrhagia. The disease can be caused by mutations in the GP6 gene, leading to the production of no glycoprotein VI (GPVI) protein, an abnormally short, nonfunctional GPVI protein; or a protein that is less able to bind to collagen. Without GPVI binding to collagen, platelets cannot come together efficiently to form a clot. The disease may also be acquired rather than inherited and such cases are associated with autoimmune disorders such as systemic lupus erythematosus (SLE). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Bleeding disorder due to glycoprotein VI deficiency (disorder) | a pour interprétation (attribut) | anormal | false | Inferred relationship | Some | 2 | |
| Bleeding disorder due to glycoprotein VI deficiency (disorder) | interprète (attribut) | Hemostatic function (observable entity) | false | Inferred relationship | Some | 2 | |
| Bleeding disorder due to glycoprotein VI deficiency (disorder) | localisation d'une constatation (attribut) | structure d'un système corporel | true | Inferred relationship | Some | 1 | |
| Bleeding disorder due to glycoprotein VI deficiency (disorder) | a pour interprétation (attribut) | anormal | true | Inferred relationship | Some | 2 | |
| Bleeding disorder due to glycoprotein VI deficiency (disorder) | interprète (attribut) | Hemostatic function (observable entity) | true | Inferred relationship | Some | 2 | |
| Bleeding disorder due to glycoprotein VI deficiency (disorder) | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | 1 | |
| Bleeding disorder due to glycoprotein VI deficiency (disorder) | est un(e) (attribut) | Platelet membrane defect | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR