Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2018. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3636281015 | Atypical cystic fibrosis (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3636282010 | Atypical cystic fibrosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Atypical cystic fibrosis | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Existential restriction modifier | ||
| Atypical cystic fibrosis | Is a | Cystic fibrosis | true | Inferred relationship | Existential restriction modifier | ||
| Atypical cystic fibrosis | Is a | Hereditary disorder by system | false | Inferred relationship | Existential restriction modifier | ||
| Atypical cystic fibrosis | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 2 | |
| Atypical cystic fibrosis | Interprets | Mucociliary clearance, function | true | Inferred relationship | Existential restriction modifier | 2 | |
| Atypical cystic fibrosis | Associated morphology | Defect | true | Inferred relationship | Existential restriction modifier | 3 | |
| Atypical cystic fibrosis | Finding site | Respiratory tract structure | true | Inferred relationship | Existential restriction modifier | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR