Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
204787019 | Deficiency of unsaturated acyl-CoA hydratase | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
204788012 | Deficiency of enoyl hydrase | en | Synonym | Active | Case insensitive | SNOMED CT core |
204789016 | Deficiency of enoyl-CoA hydratase | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2162095014 | Enoyl-CoA hydratase deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2970891018 | Deficiency of enoyl-coenzyme A hydratase | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2971656016 | Deficiency of enoyl-coenzyme A hydratase (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Deficiency of enoyl-CoA hydratase | Is a | Specific enzyme deficiency | true | Inferred relationship | Some | ||
Deficiency of enoyl-CoA hydratase | Is a | Mitochondrial trifunctional protein deficiency | true | Inferred relationship | Some | ||
Deficiency of enoyl-CoA hydratase | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Deficiency of enoyl-CoA hydratase | Finding site | Body system structure | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set