Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
115650017 | Adenosylcobalamin synthesis defect | en | Synonym | Active | Case insensitive | SNOMED CT core |
115652013 | Methylmalonic aciduria, type II | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
1216875018 | Methylmalonic acidaemia due to defects in adenosylcobalamin biosynthesis | en | Synonym | Active | Case insensitive | SNOMED CT core |
1216877014 | Vitamin B12-responsive methylmalonic acidaemia | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
1218362019 | Methylmalonic acidemia due to defects in adenosylcobalamin biosynthesis | en | Synonym | Active | Case insensitive | SNOMED CT core |
1218363012 | Vitamin B12-responsive methylmalonic acidemia | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
809579010 | Adenosylcobalamin synthesis defect (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Adenosylcobalamin synthesis defect | Is a | Methylmalonic acidaemia | true | Inferred relationship | Some | ||
Adenosylcobalamin synthesis defect | Occurrence | Congenital | false | Inferred relationship | Some | ||
Adenosylcobalamin synthesis defect | Finding site | Body system structure | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Cobalamin A disease | Is a | True | Adenosylcobalamin synthesis defect | Inferred relationship | Some | |
Cobalamin B disease | Is a | True | Adenosylcobalamin synthesis defect | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set