Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3008116014 | Pseudohypoaldosteronism type 2A | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3008144010 | Gordon hyperkalemia-hypertension syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3008151018 | Pseudohypoaldosteronism type 2A (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3008177014 | Gordon hyperkalaemia-hypertension syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3008221015 | An autosomal dominant disease characterized by increased serum potassium levels, hypertension, short stature, increased urinary calcium excretion and hyperchloremic metabolic acidosis. | en | Definition | Active | Case sensitive | SNOMED CT core |
3008224011 | An autosomal dominant disease characterised by increased serum potassium levels, hypertension, short stature, increased urinary calcium excretion and hyperchloraemic metabolic acidosis. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Pseudohypoaldosteronism type 2A | Is a | Pseudohypoaldosteronism, type 2 | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set