Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 26026013 | Familial hypoalphalipoproteinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 26027016 | Tangier disease | en | Synonym | Inactive | Case sensitive | SNOMED CT core |
| 26028014 | Familial HDL deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 26029018 | Familial high density lipoprotein deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 26030011 | Alphalipoproteinemia neuropathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 26031010 | Cholesterol thesaurismosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 26033013 | Analphalipoproteinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 477325012 | Familial hypoalphalipoproteinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 477326013 | Analphaliproteinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 477327016 | A - alphalipoproteinaemia neuropathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 477328014 | A - alphalipoproteinemia neuropathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 477329018 | Analphaliproteinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 477330011 | Alphalipoproteinaemia neuropathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 477331010 | Analphalipoproteinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 742147010 | Familial hypoalphalipoproteinemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial hypoalphalipoproteinaemia | Is a | Familial lipoprotein deficiency | true | Inferred relationship | Some | ||
| Familial hypoalphalipoproteinaemia | Is a | Lipoprotein deficiency disorder | true | Inferred relationship | Some | ||
| Familial hypoalphalipoproteinaemia | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Familial hypoalphalipoproteinaemia | Finding site | Body system structure | false | 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