Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 787710013 | Familial lipoprotein deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 83235013 | Familial lipoprotein deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial lipoprotein deficiency | Is a | Inborn error of lipoprotein metabolism | true | Inferred relationship | Some | ||
| Familial lipoprotein deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Familial lipoprotein deficiency | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial hypoalphalipoproteinaemia | Is a | True | Familial lipoprotein deficiency | Inferred relationship | Some | |
| Familial hypobetalipoproteinaemia | Is a | True | Familial lipoprotein deficiency | Inferred relationship | Some | |
| Tangier disease | Is a | True | Familial lipoprotein deficiency | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR