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 |
| 148520014 | Tetrahydrofolate methyltransferase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 148521013 | THF methyltransferase deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 832501014 | Tetrahydrofolate methyltransferase deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Tetrahydrofolate methyltransferase deficiency | est un(e) (attribut) | Enzymopathy | true | Inferred relationship | Some | ||
| Tetrahydrofolate methyltransferase deficiency | est un(e) (attribut) | Disorder of sulphur-bearing amino acid metabolism | true | Inferred relationship | Some | ||
| Tetrahydrofolate methyltransferase deficiency | est un(e) (attribut) | Inherited disorder of folate metabolism (disorder) | true | Inferred relationship | Some | ||
| Tetrahydrofolate methyltransferase deficiency | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Tetrahydrofolate methyltransferase deficiency | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR