Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 445172013 | Disorder of serine metabolism | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 699275017 | Disorder of serine metabolism (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Disorder of serine metabolism | Is a | Disorder of amino acid metabolism | false | Inferred relationship | Some | ||
| Disorder of serine metabolism | Is a | Disorder of amino acid and organic acid metabolism | true | Inferred relationship | Some | ||
| Disorder of serine metabolism | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Disorder of serine metabolism | Occurrence | Congenital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| 3-Phosphoglycerate dehydrogenase deficiency | Is a | True | Disorder of serine metabolism | Inferred relationship | Some | |
| Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome | Is a | True | Disorder of serine metabolism | Inferred relationship | Some | |
| Deficiency of phosphoserine aminotransferase | Is a | True | Disorder of serine metabolism | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR