Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 792879017 | Hereditary xanthinuria (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 90786016 | Hereditary xanthinuria | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary xanthinuria | Is a | Hereditary disease | false | Inferred relationship | Some | ||
| Hereditary xanthinuria | Is a | Hereditary metabolic disease | true | Inferred relationship | Some | ||
| Hereditary xanthinuria | Is a | Disorder of purine metabolism | true | Inferred relationship | Some | ||
| Hereditary xanthinuria | Is a | Enzymopathy | true | Inferred relationship | Some | ||
| Hereditary xanthinuria | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hereditary xanthinuria | Occurrence | Congenital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary xanthinuria type 1 | Is a | True | Hereditary xanthinuria | Inferred relationship | Some | |
| Combined molybdoflavoprotein enzyme deficiency | Is a | True | Hereditary xanthinuria | Inferred relationship | Some | |
| Isolated xanthine oxidase deficiency | Is a | True | Hereditary xanthinuria | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
FHIR