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 |
333013 | Sickle cell anemia with coexistent alpha-thalassemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
474038016 | Sickle cell anaemia with coexistent alpha-thalassaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
731084010 | Sickle cell anemia with coexistent alpha-thalassemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Sickle cell anemia with coexistent alpha-thalassemia | Is a | Sickle cell-thalassemia disease | true | Inferred relationship | Some | ||
Sickle cell anemia with coexistent alpha-thalassemia | Finding site | Erythrocyte | false | Inferred relationship | Some | ||
Sickle cell anemia with coexistent alpha-thalassemia | Causative agent | Hemoglobin S | true | Inferred relationship | Some | 5 | |
Sickle cell anemia with coexistent alpha-thalassemia | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
Sickle cell anemia with coexistent alpha-thalassemia | Associated morphology | Drepanocyte | false | Inferred relationship | Some | 1 | |
Sickle cell anemia with coexistent alpha-thalassemia | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | 1 | |
Sickle cell anemia with coexistent alpha-thalassemia | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | 1 | |
Sickle cell anemia with coexistent alpha-thalassemia | Has definitional manifestation | Erythropenia | false | Inferred relationship | Some | ||
Sickle cell anemia with coexistent alpha-thalassemia | Associated morphology | Drepanocyte | false | Inferred relationship | Some | 1 | |
Sickle cell anemia with coexistent alpha-thalassemia | Associated morphology | Drepanocyte | false | Inferred relationship | Some | 2 | |
Sickle cell anemia with coexistent alpha-thalassemia | Finding site | Erythroid cell (cell) | false | Inferred relationship | Some | 1 | |
Sickle cell anemia with coexistent alpha-thalassemia | Is a | Sickle cell-hemoglobin SS disease | true | Inferred relationship | Some | ||
Sickle cell anemia with coexistent alpha-thalassemia | Is a | Alpha thalassemia (disorder) | true | Inferred relationship | Some | ||
Sickle cell anemia with coexistent alpha-thalassemia | Associated morphology | Drepanocyte | true | Inferred relationship | Some | 1 | |
Sickle cell anemia with coexistent alpha-thalassemia | Finding site | Hematopoietic system structure | true | Inferred relationship | Some | 1 | |
Sickle cell anemia with coexistent alpha-thalassemia | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
Sickle cell anemia with coexistent alpha-thalassemia | Interprets | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 2 | |
Sickle cell anemia with coexistent alpha-thalassemia | Has interpretation | Below reference range | false | Inferred relationship | Some | 3 | |
Sickle cell anemia with coexistent alpha-thalassemia | Interprets | Red blood cell count | false | Inferred relationship | Some | 3 | |
Sickle cell anemia with coexistent alpha-thalassemia | Occurrence | Congenital | true | Inferred relationship | Some | 4 | |
Sickle cell anemia with coexistent alpha-thalassemia | Finding site | Erythrocyte | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets