Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2995184011 | Chylomicron retention disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
2995232014 | Lipid transport defect of intestine | en | Synonym | Active | Case insensitive | SNOMED CT core |
2995490019 | Chylomicron retention disease (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
2995599016 | Anderson syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
2995972013 | An autosomal recessive disorder of severe fat malabsorption associated with failure to thrive in infancy. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Chylomicron retention disease | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set