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 |
| 141631019 | Disorder of pyrimidine metabolism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 141632014 | Disorder of pyrimidine metabolism, NOS | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 827499018 | Disorder of pyrimidine metabolism (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 890761000172113 | trouble du métabolisme de la pyrimidine | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Disorder of pyrimidine metabolism | Is a | Inborn error of metabolism | false | Inferred relationship | Some | ||
| Disorder of pyrimidine metabolism | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Disorder of pyrimidine metabolism | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Disorder of pyrimidine metabolism | Is a | Metabolic disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Cytosine diphosphate choline phosphotransferase deficiency (disorder) | Is a | True | Disorder of pyrimidine metabolism | Inferred relationship | Some | |
| Dihydropyrimidinase deficiency | Is a | True | Disorder of pyrimidine metabolism | Inferred relationship | Some | |
| Beta-aminoisobutyric aciduria (disorder) | Is a | True | Disorder of pyrimidine metabolism | Inferred relationship | Some | |
| Orotic aciduria | Is a | True | Disorder of pyrimidine metabolism | Inferred relationship | Some | |
| Dihydropyrimidine dehydrogenase deficiency | Is a | True | Disorder of pyrimidine metabolism | Inferred relationship | Some | |
| Solute carrier family 35 member A1 congenital disorder of glycosylation (disorder) | Is a | True | Disorder of pyrimidine metabolism | Inferred relationship | Some | |
| Mitochondrial deoxyribonucleic acid depletion syndrome myopathic form (disorder) | Is a | True | Disorder of pyrimidine metabolism | Inferred relationship | Some |
This concept is not in any reference sets
FHIR