Status: current, Primitive. Date: 31-Jul 2020. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3902092010 | Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency classic form (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3902093017 | Congenital lipoid adrenal hyperplasia due to STAR deficiency classic form | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3902094011 | Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency classic form | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency classic form | Finding site | Adrenal cortex structure | true | Inferred relationship | Some | 1 | |
| Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency classic form | Associated morphology | Hyperplasia | true | Inferred relationship | Some | 1 | |
| Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency classic form | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency classic form | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency classic form | Is a | Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency | true | 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