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Congenital primary megaureter (disorder)
Congenital primary megaureter
Congenital primary megalo-ureter
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.
congenitale primaire mega-ureter
congenitale primaire megalo-ureter
Id717459000
StatusPrimitive
Associated morphologyDilatation
Finding siteUreteric structure
OccurrenceCongenital
Pathological processPathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ62.2
RuleTRUE
AdviceALWAYS Q62.2
CorrelationSNOMED CT source code to target map code correlation not specified