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 |
| 293150010 | Disturbance of glutamine metabolism | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 2818112011 | Disorder of glutamine metabolism | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 2818117017 | Disorder of glutamine metabolism (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Disorder of glutamine metabolism | Is a | Disorder of amino acid and organic acid metabolism | true | Inferred relationship | Existential restriction modifier | ||
| Disorder of glutamine metabolism | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Disorder of glutamine metabolism | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Neonatal epileptic encephalopathy due to deficiency of glutaminase | Is a | True | Disorder of glutamine metabolism | Inferred relationship | Existential restriction modifier | |
| Spastic ataxia, dysarthria due to glutaminase deficiency | Is a | True | Disorder of glutamine metabolism | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR