Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 114737015 | Propionic acidemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 114738013 | Propionic acidemia, NOS | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 1783835018 | Ketotic glycinaemia, types I and II | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 1783836017 | Hyperglycinaemia with ketosis AND leucopenia, types I AND/OR II | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 1783837014 | Hyperglycinaemia with ketosis and leucopenia, types I and II | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 1784223019 | Ketotic glycinemia, types I and II | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 1784224013 | Hyperglycinemia with ketosis and leukopenia, types I and II | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 1784225014 | Hyperglycinemia with ketosis AND leukopenia, types I AND/OR II | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 1788119013 | Propionyl-CoA carboxylase deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 1788120019 | PCC - Propionyl-CoA carboxylase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 4553891013 | Propionic aciduria | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 501179016 | Propionic acidemia, type I AND/OR type II | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 501180018 | Ketotic glycinemia, types I AND/OR II | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 501181019 | Ketotic glycinaemia, types I AND/OR II | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 501182014 | Propionic acidaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 501183016 | Propionic acidaemia, type I AND/OR type II | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 501184010 | Ketotic glycinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 501185011 | Ketotic hyperglycinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 501186012 | Hyperglycinaemia with ketosis and leucopenia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 501187015 | Hyperglycinemia with ketosis and leukopenia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 501188013 | Ketotic glycinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 501189017 | Ketotic hyperglycinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 808985015 | Propionic acidemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Propionic acidaemia | Is a | Disorder of branched-chain amino acid metabolism | true | Inferred relationship | Some | ||
| Propionic acidaemia | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Propionic acidaemia | Is a | Enzymopathy | true | Inferred relationship | Some | ||
| Propionic acidaemia | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Propionic acidaemia | Is a | Acidaemia | true | Inferred relationship | Some | ||
| Propionic acidaemia | Is a | Disorder of propionate AND/OR methylmalonate metabolism | true | Inferred relationship | Some | ||
| Propionic acidaemia | Is a | Non-amino organic acidaemia AND/OR aciduria | true | Inferred relationship | Some | ||
| Propionic acidaemia | Is a | Inborn error of metabolism | true | Inferred relationship | Some | ||
| Propionic acidaemia | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Biotin-(propionyl-CoA-carboxylase) ligase deficiency | Is a | False | Propionic acidaemia | Inferred relationship | Some | |
| Propionyl-CoA carboxylase deficiency | Is a | False | Propionic acidaemia | Inferred relationship | Some | |
| Propionyl-CoA carboxylase deficiency pccA complementation group | Is a | True | Propionic acidaemia | Inferred relationship | Some | |
| Propionyl-CoA carboxylase deficiency pccBC complementation group | Is a | True | Propionic acidaemia | Inferred relationship | Some | |
| Propionic acidaemia, type I | Is a | True | Propionic acidaemia | Inferred relationship | Some | |
| Propionic acidaemia, type II | Is a | True | Propionic acidaemia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set