715192004: Idiopathic achalasia of esophagus (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Finding of oesophagus\Disorder of oesophagus\Oesophageal dysmotility\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Viscus structure finding\Abdominal organ finding\Stomach finding\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus

\Digestive system finding\Gastrointestinal tract finding\Finding of oesophagus\Disorder of oesophagus\Oesophageal dysmotility\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Digestive system finding\Gastrointestinal tract finding\Disorder of gastrointestinal tract\Disorder of upper gastrointestinal tract\Disorder of oesophagus\Oesophageal dysmotility\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Digestive system finding\Gastrointestinal tract finding\Disorder of gastrointestinal tract\Disorder of upper gastrointestinal tract\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Digestive system finding\Gastrointestinal tract finding\Stomach finding\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Digestive system finding\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Disorder of upper gastrointestinal tract\Disorder of oesophagus\Oesophageal dysmotility\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Digestive system finding\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Disorder of upper gastrointestinal tract\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Digestive system finding\Disorder of digestive system\Disorder of digestive tract\Disorder of upper digestive tract\Disorder of upper gastrointestinal tract\Disorder of oesophagus\Oesophageal dysmotility\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Digestive system finding\Disorder of digestive system\Disorder of digestive tract\Disorder of upper digestive tract\Disorder of upper gastrointestinal tract\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of oesophagus\Oesophageal dysmotility\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Stomach finding\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus

\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Disorder of upper gastrointestinal tract\Disorder of oesophagus\Oesophageal dysmotility\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Disorder of upper gastrointestinal tract\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive tract\Disorder of upper digestive tract\Disorder of upper gastrointestinal tract\Disorder of oesophagus\Oesophageal dysmotility\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive tract\Disorder of upper digestive tract\Disorder of upper gastrointestinal tract\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Disorder of oesophagus\Oesophageal dysmotility\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of stomach\Achalasia of oesophagus\Idiopathic achalasia of oesophagus
\Disease\Idiopathic disease\Idiopathic achalasia of oesophagus

Status: current, Primitive. 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 Case insensitive SNOMED CT core

3301826011 Idiopathic achalasia of esophagus en Synonym Active Case insensitive SNOMED CT core

3301827019 Idiopathic achalasia of oesophagus en Synonym Active Case insensitive SNOMED CT core

3301828012 Idiopathic achalasia en Synonym Active Case insensitive SNOMED CT core

3301829016 Primary achalasia en Synonym Active Case insensitive SNOMED CT core

3301830014 Achalasia cardia en Synonym Active Case insensitive 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 Case sensitive 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 Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Idiopathic achalasia of oesophagus	Is a	Idiopathic disease	true	Inferred relationship	Some
Idiopathic achalasia of oesophagus	Is a	Achalasia of oesophagus	true	Inferred relationship	Some
Idiopathic achalasia of oesophagus	Finding site	Cardio-oesophageal junction structure	true	Inferred relationship	Some	2
Idiopathic achalasia of oesophagus	Finding site	Oesophageal structure	false	Inferred relationship	Some	1
Idiopathic achalasia of oesophagus	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Idiopathic achalasia of oesophagus	Interprets	Motility	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3301825010	Idiopathic achalasia of esophagus (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3301826011	Idiopathic achalasia of esophagus	en	Synonym	Active	Case insensitive	SNOMED CT core
3301827019	Idiopathic achalasia of oesophagus	en	Synonym	Active	Case insensitive	SNOMED CT core
3301828012	Idiopathic achalasia	en	Synonym	Active	Case insensitive	SNOMED CT core
3301829016	Primary achalasia	en	Synonym	Active	Case insensitive	SNOMED CT core
3301830014	Achalasia cardia	en	Synonym	Active	Case insensitive	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	Case sensitive	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	Case sensitive	SNOMED CT core