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 |
| 2971387014 | Complete deficiency of methylmalonyl-coenzyme A mutase (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2971787011 | Complete deficiency of methylmalonyl-coenzyme A mutase | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 356623016 | Mutase0 methylmalonic acidemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 356624010 | Complete deficiency of methylmalonyl-CoA mutase | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 356625011 | Mutase0 methylmalonic acidaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Complete deficiency of methylmalonyl-coenzyme A mutase (disorder) | est un(e) (attribut) | Deficiency of methylmalonyl-CoA mutase | true | Inferred relationship | Some | ||
| Complete deficiency of methylmalonyl-coenzyme A mutase (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Complete deficiency of methylmalonyl-coenzyme A mutase (disorder) | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Complete deficiency of methylmalonyl-coenzyme A mutase (disorder) | est un(e) (attribut) | Methylmalonyl-CoA mutase deficiency | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR