Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 476118018 | Functional defects of methionine synthase | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 740096014 | Functional defects of methionine synthase (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Functional defects of methionine synthase | Is a | Disorder of sulfur-bearing amino acid metabolism | true | Inferred relationship | Some | ||
| Functional defects of methionine synthase | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Functional defects of methionine synthase | Occurrence | Congenital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Deficiency of Cobalamin E | Is a | True | Functional defects of methionine synthase | Inferred relationship | Some | |
| Deficiency of Cobalamin G | Is a | True | Functional defects of methionine synthase | Inferred relationship | Some | |
| Homocystinuria without methylmalonic aciduria | Is a | True | Functional defects of methionine synthase | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
FHIR