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 |
| 356681017 | Disorder of pyruvate metabolism and mitochondrial respiratory chain | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 626794018 | Disorder of pyruvate metabolism and mitochondrial respiratory chain (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 6011571000146112 | stoornis van pyruvaatmetabolisme en mitochondriale ademhalingsketen | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6011581000146114 | stoornis van pyruvaatmetabolisme en mitochondriale ademhalingsketen (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Disorder of pyruvate metabolism and mitochondrial respiratory chain | Is a | Inborn error of metabolism | true | Inferred relationship | Some | ||
| Disorder of pyruvate metabolism and mitochondrial respiratory chain | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Disorder of pyruvate metabolism and mitochondrial respiratory chain | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Myoclonic epilepsy with ragged red fibers | Is a | False | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some | |
| Lactate dehydrogenase deficiency | Is a | True | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some | |
| Fumarate hydratase deficiency | Is a | True | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some | |
| Neurogenic muscle weakness, ataxia and retinitis pigmentosa (disorder) | Is a | True | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some | |
| Pearson's syndrome | Is a | True | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some | |
| Disorder of mitochondrial respiratory chain complexes | Is a | True | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some | |
| Kearns-Sayre syndrome (disorder) | Is a | True | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some | |
| Dihydrolipoamide dehydrogenase deficiency | Is a | True | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some | |
| Pyruvate dehydrogenase complex deficiency | Is a | False | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some | |
| Phosphoenolpyruvate carboxykinase (GTP) deficiency | Is a | False | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some | |
| Leber's optic atrophy | Is a | True | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some | |
| Pyruvate carboxylase deficiency | Is a | False | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some | |
| Disorders of pyruvate metabolism and gluconeogenesis | Is a | True | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some | |
| Inborn error of pyruvate metabolism | Is a | True | Disorder of pyruvate metabolism and mitochondrial respiratory chain | Inferred relationship | Some |
This concept is not in any reference sets
FHIR