Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 293235014 | L-xylulose reductase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 293236010 | L-xylulosuria | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 293237018 | Xylitol dehydrogenase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 293238011 | Essential pentosuria | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2967375010 | Essential benign pentosuria | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 574387018 | Essential pentosuria (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Essential pentosuria | Is a | Disorder of carbohydrate metabolism | false | Inferred relationship | Some | ||
| Essential pentosuria | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Essential pentosuria | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Essential pentosuria | Is a | Pentose disorder | true | Inferred relationship | Some | ||
| Essential pentosuria | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Essential pentosuria | Is a | Enzymopathy | true | Inferred relationship | Some | ||
| Essential pentosuria | Is a | Inborn error of metabolism | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
FHIR