Status: current, Primitive. Date: 31-Jul 2010. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2870387019 | Disorder of valine metabolism (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 2870886015 | Disorder of valine metabolism | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Disorder of valine metabolism | Is a | Disorder of branched-chain amino acid metabolism | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Valinosis | Is a | True | Disorder of valine metabolism | Inferred relationship | Some | |
| Deficiency of valine-tRNA ligase | Is a | True | Disorder of valine metabolism | Inferred relationship | Some | |
| Beta-hydroxyisobutyryl-CoA deacylase deficiency | Is a | False | Disorder of valine metabolism | Inferred relationship | Some | |
| Isobutyrylglycinuria | Is a | True | Disorder of valine metabolism | Inferred relationship | Some | |
| 3-Hydroxyisobutyric aciduria | Is a | True | Disorder of valine metabolism | Inferred relationship | Some | |
| Hypervalinaemia | Is a | True | Disorder of valine metabolism | Inferred relationship | Some | |
| Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency | Is a | True | Disorder of valine metabolism | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
FHIR