Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2005. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2547036015 | Sickle cell-thalassemia disease with crisis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2549357014 | Sickle cell-thalassemia disease with crisis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2549358016 | Sickle cell-thalassaemia disease with crisis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Sickle cell-thalassemia disease with crisis (disorder) | Is a | Hemoglobin S sickling disorder with crisis (disorder) | true | Inferred relationship | Some | ||
Sickle cell-thalassemia disease with crisis (disorder) | Is a | Sickle cell-thalassemia disease | true | Inferred relationship | Some | ||
Sickle cell-thalassemia disease with crisis (disorder) | Associated morphology | Drepanocyte | false | Inferred relationship | Some | 1 | |
Sickle cell-thalassemia disease with crisis (disorder) | Has definitional manifestation | Erythropenia | false | Inferred relationship | Some | ||
Sickle cell-thalassemia disease with crisis (disorder) | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | 1 | |
Sickle cell-thalassemia disease with crisis (disorder) | Finding site | Hematopoietic system structure | true | Inferred relationship | Some | 1 | |
Sickle cell-thalassemia disease with crisis (disorder) | Associated morphology | Drepanocyte | true | Inferred relationship | Some | 1 | |
Sickle cell-thalassemia disease with crisis (disorder) | Finding site | Erythrocyte | false | Inferred relationship | Some | ||
Sickle cell-thalassemia disease with crisis (disorder) | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
Sickle cell-thalassemia disease with crisis (disorder) | Has interpretation | Below reference range | false | Inferred relationship | Some | 3 | |
Sickle cell-thalassemia disease with crisis (disorder) | Interprets | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 2 | |
Sickle cell-thalassemia disease with crisis (disorder) | Interprets | Red blood cell count | false | Inferred relationship | Some | 3 | |
Sickle cell-thalassemia disease with crisis (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 4 | |
Sickle cell-thalassemia disease with crisis (disorder) | Finding site | Erythrocyte | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Acute chest syndrome due to sickle cell thalassaemia with crisis | Due to | True | Sickle cell-thalassemia disease with crisis (disorder) | Inferred relationship | Some | 1 |
Acute sequestration of spleen due to sickle cell thalassemia with crisis (disorder) | Due to | True | Sickle cell-thalassemia disease with crisis (disorder) | Inferred relationship | Some | 2 |
This concept is not in any reference sets