FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

715192004: Idiopathic achalasia of esophagus (disorder)

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
5400793011 Idiopathic achalasia (IA) is a primary esophageal motor disorder characterized by loss of esophageal peristalsis and insufficient lower esophageal sphincter (LES) relaxation in response to deglutition. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400794017 Idiopathic achalasia (IA) is a primary oesophageal motor disorder characterised by loss of oesophageal peristalsis and insufficient lower oesophageal sphincter (LES) relaxation in response to deglutition. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3301825010 Idiopathic achalasia of esophagus (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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 Only initial character 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 Only initial character 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 Only initial character 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 Only initial character 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
5400793011 Idiopathic achalasia (IA) is a primary esophageal motor disorder characterized by loss of esophageal peristalsis and insufficient lower esophageal sphincter (LES) relaxation in response to deglutition. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400794017 Idiopathic achalasia (IA) is a primary oesophageal motor disorder characterised by loss of oesophageal peristalsis and insufficient lower oesophageal sphincter (LES) relaxation in response to deglutition. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3419041001000117 Achalasie, idiopathische de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5475081000241119 achalasie idiopathique de l'œsophage fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5475081000241119 achalasie idiopathique de l'œsophage fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3419041001000117 Achalasie, idiopathische de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Idiopathic achalasia of esophagus (disorder) Is a Idiopathic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic achalasia of esophagus (disorder) Is a Achalasia of esophagus true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic achalasia of esophagus (disorder) Finding site Cardioesophageal junction structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Idiopathic achalasia of esophagus (disorder) Finding site Oesophageal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic achalasia of esophagus (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic achalasia of esophagus (disorder) Interprets Motility (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start