Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356598013 | Disorder of ornithine metabolism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 626731012 | Disorder of ornithine metabolism (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3036948015 | Ornithine metabolism disorder | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1014781000172114 | trouble du métabolisme de l'ornithine | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Disorder of ornithine metabolism | Is a | Disorder of the urea cycle metabolism | true | Inferred relationship | Some | ||
| Disorder of ornithine metabolism | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Disorder of ornithine metabolism | Occurrence | Congenital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Ornithine aminotransferase deficiency | Is a | True | Disorder of ornithine metabolism | Inferred relationship | Some | |
| Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | Is a | True | Disorder of ornithine metabolism | Inferred relationship | Some | |
| Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome | Is a | True | Disorder of ornithine metabolism | Inferred relationship | Some |
This concept is not in any reference sets
FHIR