Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1221346019 | AS - Sickle cell trait | en | Synonym | Active | Case sensitive | SNOMED CT core |
1221347011 | Heterozygous for Hb S | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
195756013 | Drepanocytosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
2164217010 | RBC's - sickle cells present | en | Synonym | Active | Case sensitive | SNOMED CT core |
2164218017 | Sickle cells present | en | Synonym | Active | Case insensitive | SNOMED CT core |
27766012 | Sickle cell trait | en | Synonym | Active | Case insensitive | SNOMED CT core |
27767015 | Hemoglobin S-A disorder | en | Synonym | Active | Case sensitive | SNOMED CT core |
27768013 | Hemoglobin A-S genotype | en | Synonym | Active | Case sensitive | SNOMED CT core |
27769017 | Hemoglobin S trait | en | Synonym | Active | Case sensitive | SNOMED CT core |
27770016 | Heterozygous hemoglobin S | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
477774011 | Haemoglobin A-S genotype | en | Synonym | Active | Case sensitive | SNOMED CT core |
477775012 | Haemoglobin S-A disorder | en | Synonym | Active | Case sensitive | SNOMED CT core |
477776013 | Haemoglobin S trait | en | Synonym | Active | Case sensitive | SNOMED CT core |
477777016 | Heterozygous haemoglobin S | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
743422014 | Sickle cell trait (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Sickle cell trait | Is a | Haemoglobinopathy | false | Inferred relationship | Some | ||
Sickle cell trait | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
Sickle cell trait | Has definitional manifestation | Red blood cell finding | false | Inferred relationship | Some | ||
Sickle cell trait | Is a | Hereditary haemoglobin S | true | Inferred relationship | Some | ||
Sickle cell trait | Is a | Heterozygous haemoglobinopathy | true | Inferred relationship | Some | ||
Sickle cell trait | Finding site | Body system structure | false | Inferred relationship | Some | ||
Sickle cell trait | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Sickle cell trait | Finding site | Erythrocyte | true | Inferred relationship | Some | 1 | |
Sickle cell trait | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
Sickle cell trait | Finding site | Erythrocyte | false | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set