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717459000: Congenital primary megaureter (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3309412012 Congenital primary megaureter (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3309413019 Congenital primary megaureter en Synonym Active Case insensitive SNOMED CT core
3309414013 Congenital primary megalo-ureter en Synonym Active Case insensitive SNOMED CT core
3309415014 An idiopathic condition in which the bladder and bladder outlet are normal but the ureter is dilated to some extent. It may be obstructed, refluxing or unobstructed and not refluxing. Prevalence is unknown, but is the second most common cause of neonatal hydronephrosis. About half of cases are asymptomatic and are discovered on routine antenatal ultrasound. The cause is unknown but it may be due to high fetal urine outflow, changes in the ureter pre and postnatal or transient anatomical obstructions that improve with postnatal development, such as ureteral folds. Not known to be hereditary, but families with more than one affected member have been described. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital primary megaureter Pathological process Pathological developmental process true Inferred relationship Some 1
Congenital primary megaureter Associated morphology Dilatation true Inferred relationship Some 1
Congenital primary megaureter Is a Idiopathic dilation of ureter true Inferred relationship Some
Congenital primary megaureter Is a Congenital dilatation of ureter true Inferred relationship Some
Congenital primary megaureter Associated morphology Congenital dilatation false Inferred relationship Some 1
Congenital primary megaureter Occurrence Congenital true Inferred relationship Some 1
Congenital primary megaureter Finding site Ureteric structure 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

Problem/Diagnosis reference set

Description inactivation indicator reference set

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