Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 31681014 | Tryptophanuria | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 746347017 | Tryptophanuria (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Tryptophanuria | Is a | Disorder of tryptophan metabolism | true | Inferred relationship | Some | ||
| Tryptophanuria | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Tryptophanuria | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Tryptophanuria with dwarfism | Is a | True | Tryptophanuria | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR