Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 293304017 | Hypoalphalipoproteinaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 293305016 | Hypoalphalipoproteinemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 523931000241110 | hypoalphalipoprotéinémie (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 574410010 | Hypoalphalipoproteinemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 910341000172117 | hypoalphalipoprotéinémie | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypoalphalipoproteinaemia | est un(e) (attribut) | trouble de déficit en lipoprotéines | true | Inferred relationship | Some | ||
| Hypoalphalipoproteinaemia | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Hypoalphalipoproteinaemia | survenue (attribut) | congénital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Lecithin cholesterol acyltransferase deficiency | est un(e) (attribut) | True | Hypoalphalipoproteinaemia | Inferred relationship | Some | |
| Family history of hypoalphalipoproteinaemia | constatation associée (attribut) | True | Hypoalphalipoproteinaemia | Inferred relationship | Some | 1 |
This concept is not in any reference sets
FHIR