Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356790016 | Disorder of cholesterol synthesis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 626860012 | Disorder of cholesterol synthesis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Disorder of cholesterol synthesis | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Disorder of cholesterol synthesis | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Disorder of cholesterol synthesis | Is a | Disorder of lipid storage and metabolism | true | Inferred relationship | Some | ||
| Disorder of cholesterol synthesis | Is a | Disorder of cholesterol metabolism | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Chondrodysplasia punctata, X-linked dominant type | Is a | True | Disorder of cholesterol synthesis | Inferred relationship | Some | |
| Microcephaly, congenital cataract, psoriasiform dermatitis syndrome | Is a | True | Disorder of cholesterol synthesis | Inferred relationship | Some | |
| Smith-Lemli-Opitz syndrome | Is a | True | Disorder of cholesterol synthesis | Inferred relationship | Some | |
| Desmosterolosis | Is a | True | Disorder of cholesterol synthesis | Inferred relationship | Some | |
| Lathosterolosis | Is a | True | Disorder of cholesterol synthesis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR