Megacystis-megaureter syndrome

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Megacystis-megaureter syndrome

ORPHA:238637Disease

Also called Megaureter-megacystis syndrome

What it is

Megacystic-megaureter syndrome is an urinary tract malformation characterized by the presence of a massive primary non-obstructive vesicoureteral reflux and a large capacity, smooth, thin walled bladder due to the continual recycling of refluxed urine. Recurrent urinary infections are commonly associated with this condition.

Key facts

Age of onset
Infancy, Neonatal
Classified as
Disease

ICD-10 codes

Q62.7filed under a broader ICD-10 category

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

MONDO 0016548UMLS C0431752

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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