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 |
293150010 | Disturbance of glutamine metabolism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2818112011 | Disorder of glutamine metabolism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2818117017 | Disorder of glutamine metabolism (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
984831000172111 | trouble de métabolisme de la glutamine | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
900591000172119 | stoornis van glutaminemetabolisme | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
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 | Some | ||
Disorder of glutamine metabolism | Finding site | Body system structure | false | Inferred relationship | Some | ||
Disorder of glutamine metabolism | Occurrence | Congenital | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Neonatal epileptic encephalopathy due to glutaminase deficiency | Is a | True | Disorder of glutamine metabolism | Inferred relationship | Some | |
Spastic ataxia, dysarthria due to glutaminase deficiency (disorder) | Is a | True | Disorder of glutamine metabolism | Inferred relationship | Some |
Reference Sets
Description inactivation indicator reference set