Status: current, Necessary but not sufficient concept definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | Reference Sets |
| 43785019 | 5-Oxoprolinase deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core | GB English: Preferred (foundation metadata concept) |
| 43786018 | Pyroglutamate hydrolase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | GB English: Acceptable (foundation metadata concept) |
| 756529016 | 5-Oxoprolinase deficiency (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core | GB English: Preferred (foundation metadata concept) |
| 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 | Finding site | Body system structure | false | Inferred relationship | Some | ||
| 5-Oxoprolinase deficiency | Occurrence | Congenital | true | Inferred relationship | Some | ||
| 5-Oxoprolinase deficiency | Is a | Inborn error of metabolism | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR