Status: current, Defined. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2990076011 | Congenital achalasia of esophagus | en | Synonym | Active | Case insensitive | SNOMED CT core |
2990177017 | Congenital achalasia of oesophagus | en | Synonym | Active | Case insensitive | SNOMED CT core |
2990215012 | Congenital achalasia of esophagus (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital achalasia of oesophagus | Is a | Congenital disease | true | Inferred relationship | Some | ||
Congenital achalasia of oesophagus | Is a | Achalasia of oesophagus | true | Inferred relationship | Some | ||
Congenital achalasia of oesophagus | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital achalasia of oesophagus | Finding site | Cardio-oesophageal junction structure | true | Inferred relationship | Some | 1 | |
Congenital achalasia of oesophagus | Finding site | Oesophageal structure | false | Inferred relationship | Some | 2 | |
Congenital achalasia of oesophagus | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
Congenital achalasia of oesophagus | Interprets | Motility | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital cardiospasm | Is a | True | Congenital achalasia of oesophagus | Inferred relationship | Some | |
Achalasia microcephaly syndrome | Is a | True | Congenital achalasia of oesophagus | Inferred relationship | Some | |
Deafness, vitiligo, achalasia syndrome | Is a | True | Congenital achalasia of oesophagus | Inferred relationship | Some | |
Glucocorticoid deficiency with achalasia | Is a | True | Congenital achalasia of oesophagus | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set