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 |
| 99986017 | Familial hypobetalipoproteinemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 498671019 | Familial hypobetalipoproteinaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 799118017 | Familial hypobetalipoproteinemia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial hypobetalipoproteinemia | Is a | Lipoprotein deficiency disorder | true | Inferred relationship | Existential restriction modifier | ||
| Familial hypobetalipoproteinemia | Is a | Familial lipoprotein deficiency | true | Inferred relationship | Existential restriction modifier | ||
| Familial hypobetalipoproteinemia | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Familial hypobetalipoproteinemia | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial hypobetalipoproteinemia - homozygous form | Is a | True | Familial hypobetalipoproteinemia | Inferred relationship | Existential restriction modifier | |
| Familial hypobetalipoproteinemia - heterozygous form | Is a | True | Familial hypobetalipoproteinemia | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR