Status: current, Defined. Date: 31-Aug 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3011641019 | Foetus with hereditary disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 306590012 | Fetus with hereditary disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 584171016 | Fetus with hereditary disease (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 818041000036119 | Foetus with hereditary disease | en | Synonym | Inactive | Initial character case insensitive | SNOMED Clinical Terms Australian extension |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Fetus with hereditary disease | Occurrence | Fetal period | true | Inferred relationship | Some | 1 | |
| Fetus with hereditary disease | Is a | Known or suspected fetal abnormality | false | Inferred relationship | Some | ||
| Fetus with hereditary disease | Is a | Hereditary disease | true | Inferred relationship | Some | ||
| Fetus with hereditary disease | Is a | Fetal disorder | true | Inferred relationship | Some | ||
| Fetus with hereditary disease | Occurrence | Fetal period | false | Inferred relationship | Some | ||
| Fetus with hereditary disease | Finding site | Fetal structure | false | Inferred relationship | Some | ||
| Fetus with hereditary disease | Occurrence | Congenital | false | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set