Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 137795011 | Disorder of glycine metabolism | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 824633019 | Disorder of glycine metabolism (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Disorder of glycine metabolism | Is a | Disorder of amino acid and organic acid metabolism | true | Inferred relationship | Some | ||
| Disorder of glycine metabolism | Is a | Disorder of amino acid metabolism | false | Inferred relationship | Some | ||
| Disorder of glycine metabolism | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Disorder of glycine metabolism | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hyperglycinaemia | Is a | True | Disorder of glycine metabolism | Inferred relationship | Some | |
| Sarcosine dehydrogenase deficiency | Is a | True | Disorder of glycine metabolism | Inferred relationship | Some | |
| Renal glycinuria, de Vries type | Is a | False | Disorder of glycine metabolism | Inferred relationship | Some | |
| Hyperglycinaemia | Is a | False | Disorder of glycine metabolism | Inferred relationship | Some | |
| Renal glycinuria, Kaiser type | Is a | False | Disorder of glycine metabolism | Inferred relationship | Some | |
| Deficiency of dimethylglycine dehydrogenase | Is a | True | Disorder of glycine metabolism | Inferred relationship | Some | |
| Glycinuria | Is a | True | Disorder of glycine metabolism | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR