Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3302919014 | Dehydrated hereditary stomatocytosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3302920015 | Dehydrated hereditary stomatocytosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3302921016 | Hereditary xerocytosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3302922011 | A rare hemolytic anemia with manifestations of decreased red cell osmotic fragility due to a defect in cation permeability, resulting in red cell dehydration and mild to moderate compensated hemolysis. Pseudohyperkalemia (loss of potassium ions from red cells on storage at room temperature) is sometimes observed. Transmission is autosomal dominant. | en | Definition | Active | Case sensitive | SNOMED CT core |
3302923018 | A rare haemolytic anaemia with manifestations of decreased red cell osmotic fragility due to a defect in cation permeability, resulting in red cell dehydration and mild to moderate compensated haemolysis. Pseudohyperkalaemia (loss of potassium ions from red cells on storage at room temperature) is sometimes observed. Transmission is autosomal dominant. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set