Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 498671019 | Familial hypobetalipoproteinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 799118017 | Familial hypobetalipoproteinemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 99986017 | Familial hypobetalipoproteinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial hypobetalipoproteinaemia | Is a | Lipoprotein deficiency disorder | true | Inferred relationship | Some | ||
| Familial hypobetalipoproteinaemia | Is a | Familial lipoprotein deficiency | true | Inferred relationship | Some | ||
| Familial hypobetalipoproteinaemia | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Familial hypobetalipoproteinaemia | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial hypobetalipoproteinaemia - homozygous form | Is a | True | Familial hypobetalipoproteinaemia | Inferred relationship | Some | |
| Familial hypobetalipoproteinaemia - heterozygous form | Is a | True | Familial hypobetalipoproteinaemia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR