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766751007: Neuhauser anomaly (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3662488015 Neuhauser anomaly en Synonym Active Case sensitive SNOMED CT core
3662489011 Neuhauser anomaly (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3662490019 A rare cardiovascular morphological anomaly due to maldevelopment of embryonal aorta resulting in right aortic arch and left ligamentum arteriosum characterized by tracheoesophageal compression symptoms (stridor, dyspnea, dysphagia, apneic episodes, recurrent respiratory infections). en Definition Active Case sensitive SNOMED CT core
3662491015 A rare cardiovascular morphological anomaly due to maldevelopment of embryonal aorta resulting in right aortic arch and left ligamentum arteriosum characterised by tracheooesophageal compression symptoms (stridor, dyspnoea, dysphagia, apnoeic episodes, recurrent respiratory infections). en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neuhauser anomaly Pathological process Pathological developmental process true Inferred relationship Some 1
Neuhauser anomaly Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Neuhauser anomaly Associated morphology Developmental abnormality false Inferred relationship Some 1
Neuhauser anomaly Finding site Aortic arch structure true Inferred relationship Some 1
Neuhauser anomaly Is a Congenital anomaly of aortic arch true Inferred relationship Some
Neuhauser anomaly Occurrence Congenital 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

Cardiovascular finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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