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 | est un(e) (attribut) | Congenital disease | true | Inferred relationship | Some | ||
| Congenital achalasia of esophagus | est un(e) (attribut) | Achalasia of oesophagus | true | Inferred relationship | Some | ||
| Congenital achalasia of esophagus | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Congenital achalasia of esophagus | localisation d'une constatation (attribut) | Cardio-oesophageal junction structure | true | Inferred relationship | Some | 1 | |
| Congenital achalasia of esophagus | localisation d'une constatation (attribut) | œsophage (structure corporelle) | false | Inferred relationship | Some | 2 | |
| Congenital achalasia of esophagus | a pour interprétation (attribut) | anormal | true | Inferred relationship | Some | 2 | |
| Congenital achalasia of esophagus | interprète (attribut) | Motility (observable entity) | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital cardiospasm | est un(e) (attribut) | True | Congenital achalasia of esophagus | Inferred relationship | Some | |
| Achalasia microcephaly syndrome (disorder) | est un(e) (attribut) | True | Congenital achalasia of esophagus | Inferred relationship | Some | |
| Deafness, vitiligo, achalasia syndrome | est un(e) (attribut) | True | Congenital achalasia of esophagus | Inferred relationship | Some | |
| Glucocorticoid deficiency with achalasia | est un(e) (attribut) | True | Congenital achalasia of esophagus | Inferred relationship | Some |
This concept is not in any reference sets
FHIR