Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3662488015 | Neuhauser anomaly | en | Synonym | Active | Case sensitive | SNOMED CT core |
3662489011 | Neuhauser anomaly (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
3662490019 | A rare cardiovascular morphological anomaly due to maldevelopment of embryonal aorta resulting in right aortic arch and left ligamentum arteriosum characterized by tracheoesophageal compression symptoms (stridor, dyspnea, dysphagia, apneic episodes, recurrent respiratory infections). | en | Definition | Active | Case sensitive | SNOMED CT core |
3662491015 | A rare cardiovascular morphological anomaly due to maldevelopment of embryonal aorta resulting in right aortic arch and left ligamentum arteriosum characterised by tracheooesophageal compression symptoms (stridor, dyspnoea, dysphagia, apnoeic episodes, recurrent respiratory infections). | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Neuhauser anomaly | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Neuhauser anomaly | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
Neuhauser anomaly | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 1 | |
Neuhauser anomaly | Finding site | Aortic arch structure | true | Inferred relationship | Some | 1 | |
Neuhauser anomaly | Is a | Congenital anomaly of aortic arch | true | Inferred relationship | Some | ||
Neuhauser anomaly | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set