Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
203590019 | Deficiency of hypoxanthine oxidase | en | Synonym | Active | Case insensitive | SNOMED CT core |
203591015 | Deficiency of xanthine oxidase | en | Synonym | Active | Case insensitive | SNOMED CT core |
473026015 | Xanthine oxidase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
727637011 | Deficiency of xanthine oxidase (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Deficiency of xanthine oxidase | Is a | Specific enzyme deficiency | true | Inferred relationship | Some | ||
Deficiency of xanthine oxidase | Is a | Metabolic renal disease | true | Inferred relationship | Some | ||
Deficiency of xanthine oxidase | Is a | Hereditary disorder of the urinary system | false | Inferred relationship | Some | ||
Deficiency of xanthine oxidase | Is a | Purine and pyrimidine metabolism disorder | true | Inferred relationship | Some | ||
Deficiency of xanthine oxidase | Is a | Congenital anomaly of trunk | false | Inferred relationship | Some | ||
Deficiency of xanthine oxidase | Occurrence | Congenital | false | Inferred relationship | Some | ||
Deficiency of xanthine oxidase | Finding site | Kidney structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Hereditary xanthinuria type 1 | Due to | True | Deficiency of xanthine oxidase | Inferred relationship | Some | 1 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set