Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 137435012 | Sex-linked hereditary disorder | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 824362013 | Sex-linked hereditary disorder (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Sex-linked hereditary disorder | Is a | Hereditary disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Macular retinoschisis | Is a | True | Sex-linked hereditary disorder | Inferred relationship | Some | |
| X-linked hereditary disease | Is a | True | Sex-linked hereditary disorder | Inferred relationship | Some | |
| X chromosome-linked pyridoxine refractory sideroblastic anaemia | Is a | False | Sex-linked hereditary disorder | Inferred relationship | Some | |
| Ornithine carbamoyltransferase deficiency | Is a | True | Sex-linked hereditary disorder | Inferred relationship | Some | |
| Opitz-Frias syndrome | Is a | True | Sex-linked hereditary disorder | Inferred relationship | Some | |
| Juvenile retinoschisis | Is a | False | Sex-linked hereditary disorder | Inferred relationship | Some | |
| Familial chondromalacia of patella | Is a | False | Sex-linked hereditary disorder | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
FHIR