Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3437590014 | Fetal cystic fibrosis (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3437591013 | Fetal cystic fibrosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3437592018 | Foetal cystic fibrosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Fetal cystic fibrosis | Is a | Fetal disorder | false | Inferred relationship | Existential restriction modifier | ||
| Fetal cystic fibrosis | Is a | Cystic fibrosis | true | Inferred relationship | Existential restriction modifier | ||
| Fetal cystic fibrosis | Occurrence | Fetal period | true | Inferred relationship | Existential restriction modifier | 3 | |
| Fetal cystic fibrosis | Associated morphology | Defect | true | Inferred relationship | Existential restriction modifier | 1 | |
| Fetal cystic fibrosis | Finding site | Respiratory tract structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Fetal cystic fibrosis | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 2 | |
| Fetal cystic fibrosis | Interprets | Mucociliary clearance, function | true | Inferred relationship | Existential restriction modifier | 2 | |
| Fetal cystic fibrosis | Is a | Fetus with hereditary disease | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Suspected cystic fibrosis in fetus | Associated finding | True | Fetal cystic fibrosis | Inferred relationship | Existential restriction modifier | 1 |
This concept is not in any reference sets
FHIR