Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1231845018 | Saccharopine dehydrogenase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 1231846017 | Alpha-aminoadipic semialdehyde deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 498194017 | Hyperlysinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 797303018 | Hyperlysinemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 97309013 | Hyperlysinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hyperlysinaemia | Is a | Lysine and hydroxylysine metabolism disorder | true | Inferred relationship | Some | ||
| Hyperlysinaemia | Is a | Aminoacidaemia | true | Inferred relationship | Some | ||
| Hyperlysinaemia | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Hyperlysinaemia | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Periodic hyperlysinaemia | Is a | True | Hyperlysinaemia | Inferred relationship | Some | |
| Periodic hyperlysinaemia with hyperammonaemia | Is a | True | Hyperlysinaemia | Inferred relationship | Some | |
| Persistent hyperlysinaemia | Is a | True | Hyperlysinaemia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR