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