Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3011540014 | Foetus with hereditary disease with antenatal problem | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 306593014 | Fetus with hereditary disease with antenatal problem | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 584174012 | Fetus with hereditary disease with antenatal problem (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Fetus with hereditary disease with antenatal problem | Occurrence | Fetal period | true | Inferred relationship | Some | 1 | |
| Fetus with hereditary disease with antenatal problem | Is a | Fetus with hereditary disease | true | Inferred relationship | Some | ||
| Fetus with hereditary disease with antenatal problem | Is a | Disorder by body site | false | Inferred relationship | Some | ||
| Fetus with hereditary disease with antenatal problem | Occurrence | Fetal period | false | Inferred relationship | Some | ||
| Fetus with hereditary disease with antenatal problem | Finding site | Fetal structure | false | Inferred relationship | Some | ||
| Fetus with hereditary disease with antenatal problem | Occurrence | Congenital | false | 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
Description inactivation indicator reference set
REPLACED BY association reference set
FHIR