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700283004: Congenital achalasia of esophagus (disorder)


Status: current, Defined. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2990076011 Congenital achalasia of esophagus en Synonym Active Case insensitive SNOMED CT core
2990177017 Congenital achalasia of oesophagus en Synonym Active Case insensitive SNOMED CT core
2990215012 Congenital achalasia of esophagus (disorder) en Fully specified name Active Case insensitive SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital cardiospasm Is a True Congenital achalasia of oesophagus Inferred relationship Some
Achalasia microcephaly syndrome Is a True Congenital achalasia of oesophagus Inferred relationship Some
Deafness, vitiligo, achalasia syndrome Is a True Congenital achalasia of oesophagus Inferred relationship Some
Glucocorticoid deficiency with achalasia Is a True Congenital achalasia of oesophagus Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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