Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 203627016 | Deficiency of unsaturated acyl-CoA reductase | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 203628014 | Deficiency of butyryl dehydrogenase | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 203629018 | Deficiency of butyryl-CoA dehydrogenase | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 473029010 | Butyryl-CoA dehydrogenase deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 473030017 | SCAD - Short chain acyl-CoA dehydrogenase deficiency | en | Synonym | Inactive | Case sensitive | SNOMED CT core |
| 473031018 | Short chain acyl-CoA dehydrogenase deficiency | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 727659013 | Deficiency of butyryl-CoA dehydrogenase (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Deficiency of butyryl-CoA dehydrogenase | Is a | Specific enzyme deficiency | true | Inferred relationship | Some | ||
| Deficiency of butyryl-CoA dehydrogenase | Is a | Disorder of fatty acid metabolism | false | Inferred relationship | Some | ||
| Deficiency of butyryl-CoA dehydrogenase | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Deficiency of butyryl-CoA dehydrogenase | Occurrence | Congenital | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set