Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 43785019 | 5-Oxoprolinase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 43786018 | Pyroglutamate hydrolase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 756529016 | 5-Oxoprolinase deficiency (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| 5-Oxoprolinase deficiency | Is a | Disorder of the gamma-glutamyl cycle | true | Inferred relationship | Some | ||
| 5-Oxoprolinase deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| 5-Oxoprolinase deficiency | Is a | Enzymopathy | true | Inferred relationship | Some | ||
| 5-Oxoprolinase deficiency | Is a | Inborn error of metabolism | true | Inferred relationship | Some | ||
| 5-Oxoprolinase deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
| 5-Oxoprolinase deficiency | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR