Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 120732016 | Isolated xanthine oxidase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 120733014 | Classical xanthinuria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 120734015 | Hereditary xanthinuria, type I | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 812986018 | Isolated xanthine oxidase deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Isolated xanthine oxidase deficiency | Is a | Hereditary xanthinuria | true | Inferred relationship | Existential restriction modifier | ||
| Isolated xanthine oxidase deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Isolated xanthine oxidase deficiency | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Isolated xanthine oxidase deficiency | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR