Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 83235013 | Familial lipoprotein deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 787710013 | Familial lipoprotein deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial lipoprotein deficiency | Is a | Inborn error of lipoprotein metabolism | true | Inferred relationship | Existential restriction modifier | ||
| Familial lipoprotein deficiency | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Familial lipoprotein deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial hypoalphalipoproteinemia | Is a | True | Familial lipoprotein deficiency | Inferred relationship | Existential restriction modifier | |
| Familial hypobetalipoproteinemia | Is a | True | Familial lipoprotein deficiency | Inferred relationship | Existential restriction modifier | |
| Tangier disease | Is a | True | Familial lipoprotein deficiency | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR