Bilateral multicystic dysplastic kidney
disease diseaseOn 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
| Field | Value |
|---|---|
| Canonical name | bilateral multicystic dysplastic kidney |
| Mondo ID | MONDO:0019982 |
| Orphanet | 97364 |
| SNOMED CT | 717749002 |
| UMLS | C1840451 |
| MedGen | 333563 |
| GARD | 0009517 |
| 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 disorder › kidney disorder › cystic kidney disease › multicystic dysplastic kidney › bilateral 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)
| Phase | Trials |
|---|---|
| Not specified | 10 |
| PHASE2 | 3 |
| PHASE4 | 1 |
| EARLY_PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06409702 | PHASE4 | RECRUITING | Treatment of High-risk Newly Diagnosed Multiple Myeloma With Minimal Residual Disease Detection |
| NCT05536505 | PHASE2 | RECRUITING | Adjuvant Treatment Based on MRD for EGFR Mutant NSCLC |
| NCT05736978 | PHASE2 | RECRUITING | Adaptive Treatment for Acute Myeloid Leukemia Based on D14 MRD Results |
| NCT07120698 | PHASE2 | RECRUITING | Adaptive Adjuvant Sintilimab Therapy Guided by MRD (ADAPT Lung) |
| NCT07371247 | EARLY_PHASE1 | ENROLLING_BY_INVITATION | Based on ctDNA-MRD Guided Adjuvant Treatment Escalation After Definitive Chemoradiotherapy for Unresectable Locally Advanced Esophageal Squamous Cell Carcinoma: a Study on Safety and Efficacy |
| NCT06822270 | Not specified | ACTIVE_NOT_RECRUITING | Different Surgical Modalities in the Management of Pelvi-ureteric Junction Obstruction |
| NCT06918262 | Not specified | RECRUITING | Observational Clinical Study on Role of MRD in Predicting Local Therapy in Oligometastatic Breast Cancer |
| NCT07112612 | Not specified | NOT_YET_RECRUITING | Minimal Residual Disease Used in Predicting Therapeutic Efficacy in Metastatic Hormone-sensitive Prostate Cancer |
| NCT07215494 | Not specified | NOT_YET_RECRUITING | A Clinical Study on Minimal Residual Disease in Patients With Systemic Light Chain Amyloidosis |
| NCT07254156 | Not specified | NOT_YET_RECRUITING | A Study of Tumor-Agnostic MRD Detection in Stage III Colorectal Cancer |
| NCT02872662 | Not specified | COMPLETED | Individual Molecular MRD Monitoring for MDS Patients After Allo-SCT |
| NCT03620955 | Not specified | UNKNOWN | Risk-stratified Therapy Based on Molecular Cytogenetic Aberration and Treatment Response in AML |
| NCT03971305 | Not specified | UNKNOWN | A Prospective Multicenters Clinical Cohort Study of Stratified Treatment of Chinese Children With Systemic ALK(+) ALCL |
| NCT04503330 | Not specified | UNKNOWN | Buccal Mucosal Graft for the Repair of Iatrogenic Pelviureteric Junction Obstruction or Ureteric Stricture. |
| NCT07475923 | Not specified | WITHDRAWN | Molecular 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)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| CARFILZOMIB | 4 | 1 |
| DARATUMUMAB | 4 | 1 |
| LENALIDOMIDE | 4 | 1 |
| SELINEXOR | 4 | 1 |
| CHEMBL5204484 | 0 | 1 |
Related Atlas pages
- Drugs: Carfilzomib, Daratumumab, Lenalidomide, Selinexor