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 |
| 493787010 | Combined methylmalonic acidaemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 493788017 | Combined methylmalonic acidemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 7715018 | Adenosylcobalamin and methylcobalamin synthesis defect | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 781178011 | Adenosylcobalamin and methylcobalamin synthesis defect (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Adenosylcobalamin and methylcobalamin synthesis defect | est un(e) (attribut) | Methylmalonic acidaemia | true | Inferred relationship | Some | ||
| Adenosylcobalamin and methylcobalamin synthesis defect | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Adenosylcobalamin and methylcobalamin synthesis defect | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Cobalamin D disease | est un(e) (attribut) | True | Adenosylcobalamin and methylcobalamin synthesis defect | Inferred relationship | Some | |
| Cobalamin A disease | est un(e) (attribut) | True | Adenosylcobalamin and methylcobalamin synthesis defect | Inferred relationship | Some | |
| Cobalamin C disease | est un(e) (attribut) | True | Adenosylcobalamin and methylcobalamin synthesis defect | Inferred relationship | Some | |
| Inherited methylmalonic acidemia AND homocystinuria | est un(e) (attribut) | True | Adenosylcobalamin and methylcobalamin synthesis defect | Inferred relationship | Some |
This concept is not in any reference sets
FHIR