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 |
| 784433018 | Inherited disorder of folate metabolism (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 8849015 | Inherited disorder of folate metabolism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 8850015 | Inherited disorder of folate metabolism, NOS | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Inherited disorder of folate metabolism (disorder) | est un(e) (attribut) | Disorder of organic acid metabolism | true | Inferred relationship | Some | ||
| Inherited disorder of folate metabolism (disorder) | est un(e) (attribut) | Inborn error of metabolism | true | Inferred relationship | Some | ||
| Inherited disorder of folate metabolism (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Inherited disorder of folate metabolism (disorder) | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Methylene tetrahydrofolate methyltransferase reductase deficiency AND homocystinuria (disorder) | est un(e) (attribut) | True | Inherited disorder of folate metabolism (disorder) | Inferred relationship | Some | |
| 5,10-Methylenetetrahydrofolate reductase deficiency | est un(e) (attribut) | True | Inherited disorder of folate metabolism (disorder) | Inferred relationship | Some | |
| Glutamate formiminotransferase deficiency (disorder) | est un(e) (attribut) | True | Inherited disorder of folate metabolism (disorder) | Inferred relationship | Some | |
| Congenital defect of folate absorption (disorder) | est un(e) (attribut) | True | Inherited disorder of folate metabolism (disorder) | Inferred relationship | Some | |
| Tetrahydrofolate methyltransferase deficiency | est un(e) (attribut) | True | Inherited disorder of folate metabolism (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR