Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 437713019 | 3-Methylglutaconic aciduria type 2 | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 437714013 | Barth syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 692540017 | 3-Methylglutaconic aciduria type 2 (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| 3-Methylglutaconic aciduria type 2 | Is a | 3-Methylglutaconic aciduria | true | Inferred relationship | Some | ||
| 3-Methylglutaconic aciduria type 2 | Is a | X-linked recessive hereditary disease | true | Inferred relationship | Some | ||
| 3-Methylglutaconic aciduria type 2 | Is a | X-linked hereditary disease | false | Inferred relationship | Some | ||
| 3-Methylglutaconic aciduria type 2 | Finding site | Body system structure | false | Inferred relationship | Some | ||
| 3-Methylglutaconic aciduria type 2 | Occurrence | Congenital | 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
FHIR