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congenital primary megaureter - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

congenital primary megaureter

MONDO:0018960

Also known as:congenital primary megalo-ureterCGMcongenital giant megaureter

Overview

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.

Diagnosis

Biomarker and diagnostic research for congenital primary megaureter has been reported in the published literature.

Prognosis

Estimated prevalence: Unknown (Unknown prevalence).

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for congenital primary megaureter.

12 publications have been identified in PubMed for congenital primary megaureter. Research spans Case Report / Case Series (33%), Epidemiology / Natural History (25%), and Diagnostic / Biomarker (17%).

Research Type	Count	% of Total
Patient case studies	4	33%

Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 12:13 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:617

GARD

Genetic and Rare Diseases Info Center

GARD:18700

Questions for Your Care Team

→Are there specialists or centers of excellence for this condition in my area?
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congenital primary megaureter

Overview

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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