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721155007: Congenital short esophagus (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
3324473018 Congenital short esophagus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324474012 Congenital short oesophagus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324472011 Congenital short esophagus (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324472011 Congenital short esophagus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324473018 Congenital short esophagus en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324473018 Congenital short esophagus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324474012 Congenital short oesophagus en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324474012 Congenital short oesophagus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5915981000241111 œsophage court congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5915981000241111 œsophage court congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital short oesophagus Is a Congenital anomaly of esophagus true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital short oesophagus Is a Deformity (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital short oesophagus Associated morphology Abnormally short growth true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital short oesophagus Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital short oesophagus Finding site Oesophageal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital short oesophagus Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital short oesophagus Is a Congenital deformity (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital brachyesophagus, intrathoracic stomach, vertebral anomalies syndrome Is a True Congenital short oesophagus Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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