Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2020. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3890977016 | Hereditary xanthinuria type 1 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3890978014 | Hereditary xanthinuria type 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3890981016 | Xanthinuria type I | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary xanthinuria type 1 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary xanthinuria type 1 | Is a | Hereditary xanthinuria | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary xanthinuria type 1 | Due to | Deficiency of xanthine oxidase | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR