Status: retired, Primitive. Date: 31-Jul 2005. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1766213015 | Acetyl-CoA: acyltransferase deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
1777834014 | Acetyl-CoA: acyltransferase deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
1783639010 | 3-Methylhydroxybutyric acidaemia | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
1784027011 | 3-Methylhydroxybutyric acidemia | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
1786203017 | alpha-Methylacetoacetic aciduria | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Acetyl-CoA: acyltransferase deficiency | Is a | Acidaemia | false | Inferred relationship | Some | ||
Acetyl-CoA: acyltransferase deficiency | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Acetyl-CoA: acyltransferase deficiency | Is a | Inborn error of metabolism | false | Inferred relationship | Some | ||
Acetyl-CoA: acyltransferase deficiency | Is a | Non-amino organic acidaemia AND/OR aciduria | false | Inferred relationship | Some | ||
Acetyl-CoA: acyltransferase deficiency | Is a | Enzymopathy | false | Inferred relationship | Some | ||
Acetyl-CoA: acyltransferase deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
Acetyl-CoA: acyltransferase deficiency | Occurrence | Congenital | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
Description inactivation indicator reference set
SAME AS association reference set