Bilateral multicystic dysplastic kidney

disease
On this page

Also known as bilateral MCDKbilateral multicystic renal dysplasiaMRDPelvi-ureteric junction obstructionPUJO

Summary

Bilateral multicystic dysplastic kidney (MONDO:0019982) is a disease and 15 clinical trials. Top therapeutic interventions include carfilzomib, daratumumab, and lenalidomide. A subtype of multicystic dysplastic kidney — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Prevalence: Unknown (Worldwide) [Orphanet-validated]
  • Clinical trials: 15

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namebilateral multicystic dysplastic kidney
Mondo IDMONDO:0019982
Orphanet97364
SNOMED CT717749002
UMLSC1840451
MedGen333563
GARD0009517
Is cancer (heuristic)no

Also known as: bilateral MCDK · bilateral multicystic renal dysplasia · MRD · Pelvi-ureteric junction obstruction · PUJO

Disease family

This is a subtype of multicystic dysplastic kidney. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › urinary system disorderkidney disordercystic kidney diseasemulticystic dysplastic kidneybilateral multicystic dysplastic kidney

Related subtypes (1): unilateral multicystic dysplastic kidney

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 15.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified10
PHASE23
PHASE41
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06409702PHASE4RECRUITINGTreatment of High-risk Newly Diagnosed Multiple Myeloma With Minimal Residual Disease Detection
NCT05536505PHASE2RECRUITINGAdjuvant Treatment Based on MRD for EGFR Mutant NSCLC
NCT05736978PHASE2RECRUITINGAdaptive Treatment for Acute Myeloid Leukemia Based on D14 MRD Results
NCT07120698PHASE2RECRUITINGAdaptive Adjuvant Sintilimab Therapy Guided by MRD (ADAPT Lung)
NCT07371247EARLY_PHASE1ENROLLING_BY_INVITATIONBased on ctDNA-MRD Guided Adjuvant Treatment Escalation After Definitive Chemoradiotherapy for Unresectable Locally Advanced Esophageal Squamous Cell Carcinoma: a Study on Safety and Efficacy
NCT06822270Not specifiedACTIVE_NOT_RECRUITINGDifferent Surgical Modalities in the Management of Pelvi-ureteric Junction Obstruction
NCT06918262Not specifiedRECRUITINGObservational Clinical Study on Role of MRD in Predicting Local Therapy in Oligometastatic Breast Cancer
NCT07112612Not specifiedNOT_YET_RECRUITINGMinimal Residual Disease Used in Predicting Therapeutic Efficacy in Metastatic Hormone-sensitive Prostate Cancer
NCT07215494Not specifiedNOT_YET_RECRUITINGA Clinical Study on Minimal Residual Disease in Patients With Systemic Light Chain Amyloidosis
NCT07254156Not specifiedNOT_YET_RECRUITINGA Study of Tumor-Agnostic MRD Detection in Stage III Colorectal Cancer
NCT02872662Not specifiedCOMPLETEDIndividual Molecular MRD Monitoring for MDS Patients After Allo-SCT
NCT03620955Not specifiedUNKNOWNRisk-stratified Therapy Based on Molecular Cytogenetic Aberration and Treatment Response in AML
NCT03971305Not specifiedUNKNOWNA Prospective Multicenters Clinical Cohort Study of Stratified Treatment of Chinese Children With Systemic ALK(+) ALCL
NCT04503330Not specifiedUNKNOWNBuccal Mucosal Graft for the Repair of Iatrogenic Pelviureteric Junction Obstruction or Ureteric Stricture.
NCT07475923Not specifiedWITHDRAWNMolecular Surveillance In Early Breast Cancer Using The Tumor-Informed ctDNA Assay Myriad Genetics Precise MRD Test; A Prospective Observational Multicenter Study (The MRD Molecular Surveillance Study)

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CARFILZOMIB41
DARATUMUMAB41
LENALIDOMIDE41
SELINEXOR41
CHEMBL520448401