Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 16419019 | Hyperammonemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 510396013 | Hyperammonaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 837368011 | Hyperammonemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hyperammonaemia | Is a | Disorder of the urea cycle metabolism | true | Inferred relationship | Some | ||
| Hyperammonaemia | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Hyperammonaemia | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome | Is a | True | Hyperammonaemia | Inferred relationship | Some | |
| Hyperammonaemia, type III | Is a | True | Hyperammonaemia | Inferred relationship | Some | |
| Congenital hyperammonaemia, type I | Is a | False | Hyperammonaemia | Inferred relationship | Some | |
| Ornithine carbamoyltransferase deficiency | Is a | True | Hyperammonaemia | Inferred relationship | Some | |
| Hyperammonemic encephalopathy | Associated with | True | Hyperammonaemia | Inferred relationship | Some | 1 |
| Hyperinsulinism and hyperammonaemia syndrome | Is a | True | Hyperammonaemia | Inferred relationship | Some | |
| Transient hyperammonaemia in infancy | Is a | True | Hyperammonaemia | Inferred relationship | Some | |
| Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency | Due to | True | Hyperammonaemia | Inferred relationship | Some | 2 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
FHIR