Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 90786016 | Hereditary xanthinuria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 792879017 | Hereditary xanthinuria (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 790401000052111 | ärftlig xantinuri | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| 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 | ||
| Hereditary xanthinuria | Is a | Hereditary disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Combined molybdoflavoprotein enzyme deficiency | Is a | True | Hereditary xanthinuria | Inferred relationship | Some | |
| Isolated xanthine oxidase deficiency | Is a | True | Hereditary xanthinuria | Inferred relationship | Some | |
| Hereditary xanthinuria type 1 | Is a | True | Hereditary xanthinuria | Inferred relationship | Some |
Reference Sets
FHIR