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 |
| 498531019 | Deficiency of glutamate formiminotransferase | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 498532014 | Deficiency of glutamate formyltransferase | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 798639019 | Glutamate formiminotransferase deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 99269017 | Glutamate formiminotransferase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 99270016 | FIGLUria | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 99271017 | Formiminoglutamic aciduria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Glutamate formiminotransferase deficiency (disorder) | est un(e) (attribut) | Inherited disorder of folate metabolism (disorder) | true | Inferred relationship | Some | ||
| Glutamate formiminotransferase deficiency (disorder) | est un(e) (attribut) | Disorder of sulphur-bearing amino acid metabolism | true | Inferred relationship | Some | ||
| Glutamate formiminotransferase deficiency (disorder) | est un(e) (attribut) | Enzymopathy | true | Inferred relationship | Some | ||
| Glutamate formiminotransferase deficiency (disorder) | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Glutamate formiminotransferase deficiency (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Glutamate formiminotransferase deficiency (disorder) | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR