Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356598013 | Disorder of ornithine metabolism | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 626731012 | Disorder of ornithine metabolism (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3036948015 | Ornithine metabolism disorder | en | Synonym | Active | Entire term case insensitive | SNOMED CT core 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 | Existential restriction modifier | ||
| Disorder of ornithine metabolism | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Disorder of ornithine metabolism | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Ornithine oxo-acid aminotransferase deficiency | Is a | True | Disorder of ornithine metabolism | Inferred relationship | Existential restriction modifier | |
| Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | Is a | True | Disorder of ornithine metabolism | Inferred relationship | Existential restriction modifier | |
| Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome | Is a | True | Disorder of ornithine metabolism | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR