Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 494905018 | Valinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 494906017 | Hypervalinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 785208014 | Hypervalinemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 79521012 | Hypervalinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 79522017 | Valine transaminase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 79523010 | Valinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypervalinaemia | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Hypervalinaemia | Is a | Enzymopathy | true | Inferred relationship | Some | ||
| Hypervalinaemia | Is a | Disorder of branched-chain amino acid metabolism | false | Inferred relationship | Some | ||
| Hypervalinaemia | Is a | Aminoacidaemia | true | Inferred relationship | Some | ||
| Hypervalinaemia | Is a | Inborn error of metabolism | true | Inferred relationship | Some | ||
| Hypervalinaemia | Is a | Disorder of valine metabolism | true | Inferred relationship | Some | ||
| Hypervalinaemia | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Hypervalinaemia | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR