Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 784433018 | Inherited disorder of folate metabolism (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 8849015 | Inherited disorder of folate metabolism | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Inherited disorder of folate metabolism | Is a | Organic acid metabolism disorder | true | Inferred relationship | Some | ||
| Inherited disorder of folate metabolism | Is a | Inborn error of metabolism | true | Inferred relationship | Some | ||
| Inherited disorder of folate metabolism | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Inherited disorder of folate metabolism | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Methylene THF reductase deficiency AND homocystinuria | Is a | True | Inherited disorder of folate metabolism | Inferred relationship | Some | |
| 5,10-Methylenetetrahydrofolate reductase deficiency | Is a | True | Inherited disorder of folate metabolism | Inferred relationship | Some | |
| Glutamate formiminotransferase deficiency | Is a | True | Inherited disorder of folate metabolism | Inferred relationship | Some | |
| Congenital defect of folate absorption | Is a | True | Inherited disorder of folate metabolism | Inferred relationship | Some | |
| Tetrahydrofolate methyltransferase deficiency | Is a | True | Inherited disorder of folate metabolism | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR