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unilateral multicystic dysplastic kidney - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

unilateral multicystic dysplastic kidney

MONDO:0019981

Also known as:unilateral MCDKunilateral multicystic renal dysplasia

Overview

Unilateral multicystic dysplastic kidney is the form of multicystic dysplastic kidney (MCDK), a congenital anomaly of the kidney and urinary tract (CAKUT), in which one kidney is large, distended by multiple cysts, and non-functional.

Diagnosis

Biomarker and diagnostic research for unilateral multicystic dysplastic kidney 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 unilateral multicystic dysplastic kidney.

18 publications have been identified in PubMed for unilateral multicystic dysplastic kidney. Research spans Epidemiology / Natural History (56%), Case Report / Case Series (28%), and Diagnostic / Biomarker (6%).

Research Type	Count	% of Total
Disease patterns and progression	10	56%

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 5:49 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:97363

GARD

Genetic and Rare Diseases Info Center

GARD:19375

Questions for Your Care Team

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unilateral multicystic dysplastic kidney

Overview

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

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Questions for Your Care Team

Questions for Your Care Team

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