Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356634018 | 3-Methylglutaconic aciduria type 1 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 356635017 | 3-Methylglutaconyl-CoA hydratase deficiency with 3-methylglutaconic acid | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 626760015 | 3-Methylglutaconic aciduria type 1 (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| 3-Methylglutaconic aciduria type 1 | Is a | 3-Methylglutaconic aciduria | true | Inferred relationship | Existential restriction modifier | ||
| 3-Methylglutaconic aciduria type 1 | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| 3-Methylglutaconic aciduria type 1 | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| 3-Methylglutaconic aciduria type 1 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR