Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3037061014 | Non ketotic hyperglycinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3037470016 | Non ketotic hyperglycinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 356613013 | Disorder of glycine cleavage enzyme complex | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 356614019 | NKH - Non-ketotic hyperglycinaemia | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 356615018 | Non-ketotic hyperglycinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 356616017 | NKH - Non-ketotic hyperglycinemia | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 356617014 | Non-ketotic hyperglycinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 626744019 | Non-ketotic hyperglycinemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Non-ketotic hyperglycinaemia | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Non-ketotic hyperglycinaemia | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Non-ketotic hyperglycinaemia | Is a | Hyperglycinaemia | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Childhood-onset spasticity with hyperglycinaemia | Is a | True | Non-ketotic hyperglycinaemia | Inferred relationship | Some | |
| Non-ketotic hyperglycinaemia H protein deficiency | Is a | True | Non-ketotic hyperglycinaemia | Inferred relationship | Some | |
| Non-ketotic hyperglycinaemia L protein deficiency | Is a | True | Non-ketotic hyperglycinaemia | Inferred relationship | Some | |
| Infantile glycine encephalopathy | Is a | True | Non-ketotic hyperglycinaemia | Inferred relationship | Some | |
| Atypical glycine encephalopathy | Is a | True | Non-ketotic hyperglycinaemia | Inferred relationship | Some | |
| Glycine dehydrogenase (decarboxylating) deficiency | Is a | True | Non-ketotic hyperglycinaemia | Inferred relationship | Some | |
| Aminomethyltransferase deficiency | Is a | True | Non-ketotic hyperglycinaemia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
REPLACED BY association reference set
FHIR