Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 38413019 | Glutaric aciduria, type 2 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 38414013 | Ethylmalonic-adipicaciduria | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 38417018 | Glutaric acidemia, type 2 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4637156012 | MADD - multiple acyl-CoA dehydrogenase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 481457011 | Glutaric aciduria type II | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 481458018 | MAD - Multiple acyl-CoA dehydrogenase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 481460016 | Glutaric acidaemia, type 2 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 752344016 | Glutaric aciduria, type 2 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Glutaric aciduria, type 2 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Glutaric aciduria, type 2 | Is a | Disorder of fatty acid metabolism | true | Inferred relationship | Some | ||
| Glutaric aciduria, type 2 | Is a | Glutaric aciduria | true | Inferred relationship | Some | ||
| Glutaric aciduria, type 2 | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Glutaric aciduria, type 2 | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Beta chain electron transfer flavoprotein deficiency | Is a | True | Glutaric aciduria, type 2 | Inferred relationship | Some | |
| Alpha chain electron transfer flavoprotein deficiency | Is a | True | Glutaric aciduria, type 2 | Inferred relationship | Some | |
| Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency | Is a | True | Glutaric aciduria, type 2 | Inferred relationship | Some | |
| X-linked glutaric aciduria, type 2 | Is a | False | Glutaric aciduria, type 2 | Inferred relationship | Some | |
| Autosomal recessive glutaric aciduria, type 2 | Is a | False | Glutaric aciduria, type 2 | Inferred relationship | Some | |
| Transient neonatal multiple acyl-CoA dehydrogenase deficiency | Is a | False | Glutaric aciduria, type 2 | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR