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 |
| 445173015 | 3-Phosphoglycerate dehydrogenase deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 602581000241111 | déficit en 3-phosphoglycerate déshydrogénase (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 699276016 | 3-Phosphoglycerate dehydrogenase deficiency (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 993481000172113 | déficit en 3-phosphoglycerate déshydrogénase | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| 3-Phosphoglycerate dehydrogenase deficiency | est un(e) (attribut) | Disorder of serine metabolism | true | Inferred relationship | Some | ||
| 3-Phosphoglycerate dehydrogenase deficiency | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| 3-Phosphoglycerate dehydrogenase deficiency | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Neu-Laxova syndrome | est un(e) (attribut) | True | 3-Phosphoglycerate dehydrogenase deficiency | Inferred relationship | Some | |
| 3-phosphoglycerate dehydrogenase deficiency juvenile form (disorder) | est un(e) (attribut) | True | 3-Phosphoglycerate dehydrogenase deficiency | Inferred relationship | Some | |
| 3-phosphoglycerate dehydrogenase deficiency infantile form (disorder) | est un(e) (attribut) | True | 3-Phosphoglycerate dehydrogenase deficiency | Inferred relationship | Some |
This concept is not in any reference sets
FHIR