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721155007: Congenital short esophagus (disorder)


Status: current, Defined. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3324472011 Congenital short esophagus (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3324473018 Congenital short esophagus en Synonym Active Case insensitive SNOMED CT core
3324474012 Congenital short oesophagus en Synonym Active Case insensitive SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital short oesophagus Pathological process Pathological developmental process true Inferred relationship Some 1
Congenital short oesophagus Is a Congenital deformity true Inferred relationship Some
Congenital short oesophagus Is a Congenital anomaly of esophagus true Inferred relationship Some
Congenital short oesophagus Is a Deformity false Inferred relationship Some
Congenital short oesophagus Associated morphology Abnormally short growth true Inferred relationship Some 1
Congenital short oesophagus Occurrence Congenital true Inferred relationship Some 1
Congenital short oesophagus Finding site Oesophageal structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital brachyoesophagus, intrathoracic stomach, vertebral anomalies syndrome Is a True Congenital short oesophagus Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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