Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3301825010 | Idiopathic achalasia of esophagus (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3301826011 | Idiopathic achalasia of esophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3301827019 | Idiopathic achalasia of oesophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3301828012 | Idiopathic achalasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3301829016 | Primary achalasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3301830014 | Achalasia cardia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3302126010 | Characterized by loss of esophageal peristalsis and insufficient lower esophageal sphincter relaxation in response to deglutition. A rare disease with no gender predilection, the peak incidence occurs between 30 and 60 years of age. Although the precise etiology is unknown, it is often thought to be either autoimmune, viral immune, or neurodegenerative. Some familial cases have been reported, but the rarity of familial occurrence does not support the hypothesis that genetic inheritance is a significant etiologic factor. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3302127018 | Characterised by loss of oesophageal peristalsis and insufficient lower oesophageal sphincter relaxation in response to deglutition. A rare disease with no gender predilection, the peak incidence occurs between 30 and 60 years of age. Although the precise aetiology is unknown, it is often thought to be either autoimmune, viral immune, or neurodegenerative. Some familial cases have been reported, but the rarity of familial occurrence does not support the hypothesis that genetic inheritance is a significant aetiologic factor. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Idiopathic achalasia of esophagus (disorder) | Is a | Idiopathic disease | true | Inferred relationship | Some | ||
| Idiopathic achalasia of esophagus (disorder) | Is a | Achalasia of esophagus | true | Inferred relationship | Some | ||
| Idiopathic achalasia of esophagus (disorder) | Finding site | Cardioesophageal junction structure | true | Inferred relationship | Some | 2 | |
| Idiopathic achalasia of esophagus (disorder) | Finding site | Oesophageal structure | false | Inferred relationship | Some | 1 | |
| Idiopathic achalasia of esophagus (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Idiopathic achalasia of esophagus (disorder) | Interprets | Motility (observable entity) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR