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congenitale primaire mega-ureter (aandoening)
congenitale primaire mega-ureter
congenitale primaire megalo-ureter
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.
Id717459000
StatusPrimitive
Associated morphologydilatatie
Finding sitestructuur van ureter
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ62.2
TermCongenitale megalo-ureter
SNOMED CT to Orphanet simple map617
SNOMED CT to ICD-10 extended map
TargetQ62.2
RuleTRUE
AdviceALWAYS Q62.2
CorrelationSNOMED CT source code to target map code correlation not specified