Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2020. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 350123011 | Inherited mucociliary clearance defect | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 621875015 | Inherited mucociliary clearance defect (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 5144466017 | Inherited impaired mucociliary clearance | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 5144467014 | Inherited defective mucociliary clearance | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Inherited mucociliary clearance defect | Is a | Mucociliary clearance defect | true | Inferred relationship | Existential restriction modifier | ||
| Inherited mucociliary clearance defect | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 1 | |
| Inherited mucociliary clearance defect | Interprets | Mucociliary clearance, function | true | Inferred relationship | Existential restriction modifier | 1 | |
| Inherited mucociliary clearance defect | Associated morphology | Defect | false | Inferred relationship | Existential restriction modifier | 2 | |
| Inherited mucociliary clearance defect | Finding site | Respiratory tract structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Inherited mucociliary clearance defect | Is a | Hereditary disorder by system | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Cystic fibrosis | Is a | True | Inherited mucociliary clearance defect | Inferred relationship | Existential restriction modifier | |
| Immotile cilia syndrome | Is a | True | Inherited mucociliary clearance defect | Inferred relationship | Existential restriction modifier | |
| Immotile cilia syndrome due to excessively long cilia | Is a | True | Inherited mucociliary clearance defect | Inferred relationship | Existential restriction modifier | |
| Cystic fibrosis of pancreas | Is a | False | Inherited mucociliary clearance defect | Inferred relationship | Existential restriction modifier | |
| Primary ciliary dyskinesia and retinitis pigmentosa syndrome | Is a | True | Inherited mucociliary clearance defect | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR