Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1216348015 | CblD methylmalonic acidaemia and homocystinuria | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 1217848019 | CblD methylmalonic acidemia and homocystinuria | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 1227450016 | CblD - Cobalamin locus D | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 1227451017 | M0E.321 Cobalamin locus D variant | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 52231016 | Cobalamin D disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 762318018 | Cobalamin D disease (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Cobalamin D disease | Is a | Adenosylcobalamin and methylcobalamin synthesis defect | true | Inferred relationship | Some | ||
| Cobalamin D disease | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Cobalamin D disease | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set