Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4012457015 | Congenital pulmonary airway malformation type 0 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4012458013 | Congenital pulmonary airway malformation type 0 | en | Synonym | Active | Case insensitive | SNOMED CT core |
4013156013 | Congenital pulmonary airway malformation type 0 originates in the trachea or bronchi with acinar dysgenesis, cartilage, smooth muscles, and glands separated by mesenchyme. It is fatal after birth. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital pulmonary airway malformation type 0 | Is a | Congenital cystic adenomatoid malformation of lung | true | Inferred relationship | Some | ||
Congenital pulmonary airway malformation type 0 | Associated morphology | Cystic dilatation | true | Inferred relationship | Some | 1 | |
Congenital pulmonary airway malformation type 0 | Finding site | Lung structure | true | Inferred relationship | Some | 1 | |
Congenital pulmonary airway malformation type 0 | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital pulmonary airway malformation type 0 | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Respiratory finding reference set
Problem/Diagnosis reference set