Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 437717018 | 3-Methylglutaconic aciduria type 4 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 692543015 | 3-Methylglutaconic aciduria type 4 (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 384091000146118 | 3-methylglutaconacidurie type 4 | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 384101000146113 | 3-methylglutaconacidurie type 4 (aandoening) | nl | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| 3-Methylglutaconic aciduria type 4 | Is a | 3-Methylglutaconic aciduria | true | Inferred relationship | Some | ||
| 3-Methylglutaconic aciduria type 4 | Occurrence | Congenital | false | Inferred relationship | Some | ||
| 3-Methylglutaconic aciduria type 4 | Finding site | Body system structure | false | Inferred relationship | Some | ||
| 3-Methylglutaconic aciduria type 4 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| 3-Methylglutaconic aciduria type 4 | Is a | Hereditary metabolic disease | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome (disorder) | Is a | True | 3-Methylglutaconic aciduria type 4 | Inferred relationship | Some |
This concept is not in any reference sets
FHIR