Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 437708018 | Disorder of creatine synthesis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 692534012 | Disorder of creatine synthesis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Disorder of creatine synthesis | Is a | Disorder of amino acid metabolism | true | Inferred relationship | Some | ||
| Disorder of creatine synthesis | Is a | Inborn error of metabolism | true | Inferred relationship | Some | ||
| Disorder of creatine synthesis | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Disorder of creatine synthesis | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Deficiency of guanidinoacetate methyltransferase | Is a | True | Disorder of creatine synthesis | Inferred relationship | Some | |
| Cerebral creatine deficiency syndrome 3 | Is a | True | Disorder of creatine synthesis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR