Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 485115016 | 3-Methylhydroxybutyric acidaemia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 53563018 | Acetyl-CoA: acyltransferase deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 53564012 | 3-Ketothiolase deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 53565013 | alpha-Methylacetoacetic aciduria | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 53566014 | 3-Methylhydroxybutyric acidemia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 763292014 | Acetyl-CoA: acyltransferase deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Acetyl-CoA: acyltransferase deficiency | est un(e) (attribut) | Acidemia | false | Inferred relationship | Some | ||
| Acetyl-CoA: acyltransferase deficiency | est un(e) (attribut) | Non-amino organic acidemia AND/OR aciduria | false | Inferred relationship | Some | ||
| Acetyl-CoA: acyltransferase deficiency | est un(e) (attribut) | Enzymopathy | false | Inferred relationship | Some | ||
| Acetyl-CoA: acyltransferase deficiency | est un(e) (attribut) | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
| Acetyl-CoA: acyltransferase deficiency | est un(e) (attribut) | Inborn error of metabolism | false | Inferred relationship | Some | ||
| Acetyl-CoA: acyltransferase deficiency | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Acetyl-CoA: acyltransferase deficiency | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR