Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2013. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 92832010 | Essential benign pentosuria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 92833017 | Pentosuria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 92834011 | Xylitol dehydrogenase deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 92835012 | L-xylulose reductase deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 92836013 | L-xylulosuria | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 794253018 | Essential benign pentosuria (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Essential benign pentosuria | Is a | Enzymopathy | false | Inferred relationship | Existential restriction modifier | ||
| Essential benign pentosuria | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Existential restriction modifier | ||
| Essential benign pentosuria | Is a | Pentose disorder | false | Inferred relationship | Existential restriction modifier | ||
| Essential benign pentosuria | Is a | Inborn error of metabolism | false | Inferred relationship | Existential restriction modifier | ||
| Essential benign pentosuria | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Essential benign pentosuria | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR