Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 206336016 | Sickle cell disease | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 206337013 | Hemoglobin S-S disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 206338015 | Drepanocythemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2547671019 | Hb SS disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 2663794019 | Hereditary hemoglobinopathy disorder homozygous for hemoglobin S | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 328014 | Sickle cell anemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3688057012 | Sickle cell-hemoglobin SS disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3688058019 | Sickle cell-haemoglobin SS disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3688059010 | Sickle cell-hemoglobin SS disease (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 3780079019 | Hereditary haemoglobinopathy disorder homozygous for haemoglobin S | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 474021015 | Drepanocythaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 474022010 | Sickle cell anaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 474023017 | Haemoglobin S disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 474024011 | Haemoglobin S-S disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 474025012 | Hemoglobin S disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 474026013 | Hb S disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 474027016 | Sickle cell syndrome | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 731078012 | Hereditary hemoglobinopathy disorder homozygous for hemoglobin S (disorder) | en | Fully specified name | Inactive | Initial character case insensitive | SNOMED CT core |
Reference Sets
Emergency department reference set
Australian emergency department reference set
NSW Emergency Department reference set
Clinical finding foundation reference set
Emergency department diagnosis reference set
Problem/Diagnosis reference set