Status: current, Primitive. Date: 31-Jul 2012. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2920590011 | Congenital monosaccharide malabsorption | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2920890015 | Congenital monosaccharide malabsorption (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital monosaccharide malabsorption | Is a | Disorder of carbohydrate absorption | true | Inferred relationship | Some | ||
| Congenital monosaccharide malabsorption | Is a | Congenital disease | true | Inferred relationship | Some | ||
| Congenital monosaccharide malabsorption | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital monosaccharide malabsorption | Is a | Malabsorption syndrome | true | Inferred relationship | Some | ||
| Congenital monosaccharide malabsorption | Finding site | Gastrointestinal tract structure | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital glucose-galactose malabsorption | Is a | True | Congenital monosaccharide malabsorption | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
FHIR