Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2990076011 | Congenital achalasia of esophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2990177017 | Congenital achalasia of oesophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2990215012 | Congenital achalasia of esophagus (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital achalasia of esophagus | Is a | Congenital disease (disorder) | true | Inferred relationship | Some | ||
| Congenital achalasia of esophagus | Is a | Achalasia of esophagus | true | Inferred relationship | Some | ||
| Congenital achalasia of esophagus | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital achalasia of esophagus | Finding site | Cardioesophageal junction structure | true | Inferred relationship | Some | 1 | |
| Congenital achalasia of esophagus | Finding site | Oesophageal structure | false | Inferred relationship | Some | 2 | |
| Congenital achalasia of esophagus | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
| Congenital achalasia of esophagus | Interprets | Motility (observable entity) | true | Inferred relationship | Some | 2 | |
| Congenital achalasia of esophagus | Is a | Disorder of digestive system specific to fetus OR newborn | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital cardiospasm | Is a | True | Congenital achalasia of esophagus | Inferred relationship | Some | |
| Achalasia microcephaly syndrome (disorder) | Is a | True | Congenital achalasia of esophagus | Inferred relationship | Some | |
| Deafness, vitiligo, achalasia syndrome | Is a | True | Congenital achalasia of esophagus | Inferred relationship | Some | |
| Glucocorticoid deficiency with achalasia | Is a | True | Congenital achalasia of esophagus | Inferred relationship | Some |
This concept is not in any reference sets
FHIR