Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356906011 | Lecithin cholesterol acyltransferase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 626925017 | Lecithin cholesterol acyltransferase deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Lecithin cholesterol acyltransferase deficiency | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
| Lecithin cholesterol acyltransferase deficiency | Has definitional manifestation | Red blood cell finding | false | Inferred relationship | Some | ||
| Lecithin cholesterol acyltransferase deficiency | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Lecithin cholesterol acyltransferase deficiency | Finding site | Erythrocyte | true | Inferred relationship | Some | 1 | |
| Lecithin cholesterol acyltransferase deficiency | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
| Lecithin cholesterol acyltransferase deficiency | Is a | Congenital anomaly of the haematopoietic system | false | Inferred relationship | Some | ||
| Lecithin cholesterol acyltransferase deficiency | Is a | Erythrocyte membrane abnormality | true | Inferred relationship | Some | ||
| Lecithin cholesterol acyltransferase deficiency | Is a | Hereditary disorder of haematologic system | false | Inferred relationship | Some | ||
| Lecithin cholesterol acyltransferase deficiency | Is a | Hypoalphalipoproteinaemia | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Fish-eye disease | Is a | True | Lecithin cholesterol acyltransferase deficiency | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR