Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 791304019 | Inborn error of pyruvate metabolism (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 88491015 | Inborn error of pyruvate metabolism | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Inborn error of pyruvate metabolism | Is a | Disorder of pyruvate metabolism and mitochondrial respiratory chain | true | Inferred relationship | Some | ||
| Inborn error of pyruvate metabolism | Is a | Inborn error of metabolism | false | Inferred relationship | Some | ||
| Inborn error of pyruvate metabolism | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Inborn error of pyruvate metabolism | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Mitochondrial pyruvate carrier deficiency | Is a | True | Inborn error of pyruvate metabolism | Inferred relationship | Some | |
| Pyruvate dehydrogenase complex deficiency | Is a | True | Inborn error of pyruvate metabolism | Inferred relationship | Some | |
| Phosphoenolpyruvate carboxykinase (GTP) deficiency | Is a | True | Inborn error of pyruvate metabolism | Inferred relationship | Some | |
| Pyruvate carboxylase deficiency | Is a | True | Inborn error of pyruvate metabolism | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR