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721155007: Congenital short esophagus (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

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


1 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital brachyesophagus, intrathoracic stomach, vertebral anomalies syndrome Is a True Congenital short esophagus Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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