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 |
203590019 | Deficiency of hypoxanthine oxidase | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
203591015 | Deficiency of xanthine oxidase | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
473026015 | Xanthine oxidase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
727637011 | Deficiency of xanthine oxidase (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Deficiency of xanthine oxidase (disorder) | Is a | Specific enzyme deficiency | true | Inferred relationship | Some | ||
Deficiency of xanthine oxidase (disorder) | Is a | Metabolic renal disease | true | Inferred relationship | Some | ||
Deficiency of xanthine oxidase (disorder) | Is a | Hereditary disorder of the urinary system | false | Inferred relationship | Some | ||
Deficiency of xanthine oxidase (disorder) | Is a | Disorder of purine and pyrimidine metabolism | true | Inferred relationship | Some | ||
Deficiency of xanthine oxidase (disorder) | Is a | Congenital anomaly of trunk | false | Inferred relationship | Some | ||
Deficiency of xanthine oxidase (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
Deficiency of xanthine oxidase (disorder) | Finding site | Kidney structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Hereditary xanthinuria type 1 | Due to | False | Deficiency of xanthine oxidase (disorder) | Inferred relationship | Some | 1 |
Hereditary xanthinuria | Is a | True | Deficiency of xanthine oxidase (disorder) | Inferred relationship | Some |
This concept is not in any reference sets