Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3036948015 | Ornithine metabolism disorder | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 356598013 | Disorder of ornithine metabolism | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 626731012 | Disorder of ornithine metabolism (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Ornithine metabolism disorder | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Ornithine metabolism disorder | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Ornithine metabolism disorder | Is a | Disorder of the urea cycle metabolism | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome | Is a | True | Ornithine metabolism disorder | Inferred relationship | Some | |
| Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome | Is a | True | Ornithine metabolism disorder | Inferred relationship | Some | |
| Ornithine aminotransferase deficiency | Is a | True | Ornithine metabolism disorder | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR