Impaired renal function disease

disease
On this page

Also known as disease of kidneykidney disease

Summary

Impaired renal function disease (MONDO:0001343) is a disease with 6 GWAS associations across 10 studies and 474 clinical trials. Top therapeutic interventions include cinacalcet, darbepoetin alfa, and losartan. A subtype of kidney disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • GWAS associations: 6
  • Clinical trials: 474

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameimpaired renal function disease
Mondo IDMONDO:0001343
DOIDDOID:11705
ICD-10-CMN25
SNOMED CT197663003
UMLSC0341677
MedGen574572
Is cancer (heuristic)no

Also known as: disease of kidney · kidney disease

Data availability: 6 GWAS associations (10 studies).

Disease family

This is a subtype of kidney disorder. 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 disorderimpaired renal function disease

Related subtypes (56): renal hypertension, kidney failure, nephritis, nephrocalcinosis, atheroembolism of kidney, renal artery disease, nephrosis, cystic kidney disease, anuria, stricture or kinking of ureter, proteinuria, renal infectious disease, diabetes insipidus, orthostatic proteinuria, kidney hypertrophy, chronic kidney disease, hydronephrosis, renal tubular transport disease, kidney cortex necrosis, kidney papillary necrosis, perinephritis, renal aminoaciduria, autosomal dominant progressive nephropathy with hypertension, nephrolithiasis, X-linked diffuse leiomyomatosis-Alport syndrome, tubulointerstitial nephritis and uveitis syndrome, distal renal tubular acidosis, oligomeganephronia, duplication of urethra, renal tubular dysgenesis, exstrophy-epispadias complex, fetal lower urinary tract obstruction, IgG4-related kidney disease, congenital primary megaureter, renal nutcracker syndrome, renal hypoplasia, renal dysplasia, congenital megacalycosis, glomerular disorder, congenital renal artery stenosis, kidney neoplasm, renal tubule disorder, pyonephrosis, Arnold stickler bourne syndrome, C1q nephropathy, hypertensive nephropathy, atypical Fanconi syndrome-neonatal hyperinsulinism syndrome, idiopathic non-lupus full-house nephropathy, lachiewicz sibley syndrome, crush syndrome, obstructive nephropathy, inherited kidney disorder, acute tubulointerstitial nephritis, kidney cortex disease, non-syndromic supernumerary kidneys, neonatal renal venous thrombosis

Subtypes (4): secondary hyperparathyroidism of renal origin, hypophosphatemic nephrolithiasis/osteoporosis 1, hypophosphatemic nephrolithiasis/osteoporosis 2, nephrogenic diabetes insipidus

Genetics & variants

GWAS landscape

6 GWAS associations across 10 studies. Top hits map to 5 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
rs96223624e-31APOL1A0.27
rs96223634e-30APOL1A0.27
rs779246156e-16PDILTG0.17
rs360600363e-14UMODC0.19
rs79031463e-11TCF7L2C0.1
rs748121514e-07HRH1?

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90476136Verma A20247,038440,105Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90476135Verma A20244,035116,190Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90480387Verma A20244,035116,190Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90652092Liu TY20251,577202,534Diversity and longitudinal records: Genetic architecture of disease associations and polygenic risk in the Taiwanese Han population.
GCST90478539Verma A20241,09258,353Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90474189UK Biobank Whole-Genome Sequencing Consortium2025236458,204Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90436426Zhou W201898397,602Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
GCST90134318Dube MP202200Pharmacogenomic study of heart failure and candesartan response from the CHARM programme.
GCST90134319Dube MP202200Pharmacogenomic study of heart failure and candesartan response from the CHARM programme.
GCST90134320Dube MP202200Pharmacogenomic study of heart failure and candesartan response from the CHARM programme.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding0
Tier 2: splice/UTR0
Tier 3: regulatory0
Tier 4: intronic/intergenic6

MAF distribution

BucketVariants
common (>=0.05)6
low_freq (0.01-0.05)0
rare (<0.01)0
unknown0

Functional consequences

ConsequenceCount
intron_variant6

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
rs96223622236260398A>C0.472intron_variantAPOL14e-31Tier 4: intronic/intergenic
rs96223632236260509A>G0.108intron_variantAPOL14e-30Tier 4: intronic/intergenic
rs779246151620381010G>A0.174intron_variantPDILT6e-16Tier 4: intronic/intergenic
rs360600361620350628C>T0.163intron_variantUMOD3e-14Tier 4: intronic/intergenic
rs790314610112998590C>G,T0.292intron_variantTCF7L23e-11Tier 4: intronic/intergenic
rs74812151311209273G>A0.05intron_variantHRH14e-07Tier 4: intronic/intergenic

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: 474.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified291
PHASE444
PHASE344
PHASE241
PHASE140
PHASE1/PHASE29
PHASE2/PHASE33
EARLY_PHASE12

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05096195PHASE4ACTIVE_NOT_RECRUITINGPRevEnting FracturEs in REnal Disease - 1
NCT06291077PHASE4NOT_YET_RECRUITINGComparison of the Effects of Belatacept and Anticalcineurins on Endothelial Function in Renal Transplant Patients -
NCT06625073PHASE4RECRUITINGRandomized Trial of SGLT2i in Heart Transplant Recipients
NCT06642623PHASE4RECRUITINGA Prospective Trial of Enavogliflozin to Evaluate Cardio-renal Outcome in Type 2 Diabetes Mellitus Patients
NCT07138521PHASE4NOT_YET_RECRUITINGOptimizing Linezolid Dosing in Patients With Advanced Renal Impairment: a Therapeutic Drug Monitoring-based Evaluation
NCT07182422PHASE4RECRUITINGAST-120 (Kremezin®) for the Renal Protection and Attenuation of Decline in Acute Kidney Disease
NCT00067990PHASE4COMPLETEDAngiotensin II Blockade for Chronic Allograft Nephropathy
NCT00117078PHASE4COMPLETEDAranesp® Monthly Preference Study - 2
NCT00117130PHASE4COMPLETEDStudy to Evaluate Effectiveness of Aranesp®
NCT00132431PHASE4COMPLETEDSTART: Sensipar Treatment Algorithm to Reach K/DOQI Targets in Chronic Kidney Disease Subjects With Secondary Hyperparathyroidism
NCT00246129PHASE4COMPLETEDCamTac Trial:Campath-Tacrolimus vs IL2R MoAb/Tacrolimus/MMF in Renal Transplantation
NCT00275535PHASE4COMPLETEDThe Comparison of Tacrolimus and Sirolimus Immunosuppression Based Drug Regimens in Kidney Transplant Recipients
NCT00282217PHASE4COMPLETEDStudy Evaluating Sirolimus in the Treatment of Kidney Transplant
NCT00289614PHASE4COMPLETEDPatients With Renal Impairment and Diabetes Undergoing Computed Tomography (CT)
NCT00290069PHASE4UNKNOWNRenal Function Optimization With Mycophenolate Mofetil (MMF) Immunosuppressor Regimes (ALHAMBRA)
NCT00338468PHASE4TERMINATEDA Study to Assess Disability in Anemic Elderly Patients With Kidney Disease Receiving PROCRIT (Epoetin Alfa)
NCT00368901PHASE4COMPLETEDSTAAR-2 Clinical Study
NCT00369733PHASE4COMPLETEDSTAAR-3 Clinical Study
NCT00369772PHASE4COMPLETEDSTAAR-1 Clinical Study
NCT00379899PHASE4COMPLETEDADVANCE: Study to Evaluate Cinacalcet Plus Low Dose Vitamin D on Vascular Calcification in Subjects With Chronic Kidney Disease Receiving Hemodialysis
NCT00443508PHASE4UNKNOWNReduction or Discontinuation of CNI’s With Conversion to Everolimus-Based Immunosuppresion
NCT00452478PHASE4TERMINATEDConversion From Standard Phosphate Binder Therapy to Fosrenol® (Lanthanum Carbonate) in Chronic Kidney Disease Stage 5
NCT00492518PHASE4COMPLETEDAcetylcysteine, Theophylline, and a Combination of Both in the Prophylaxis of Contrast-Induced Nephropathy
NCT00505102PHASE4UNKNOWNSafe Renal Function In Long Term Heart Transplanted Patients
NCT00526331PHASE4COMPLETEDEvaluation of Arterial Pressure Based Cardiac Output for Goal-Directed Perioperative Therapy
NCT00688480PHASE4COMPLETEDDo Xanthine Oxidase Inhibitors Reduce Both Left Ventricular Hypertrophy and Endothelial Dysfunction in Cardiovascular Patients With Renal Dysfunction?
NCT00863707PHASE4COMPLETEDA Study of the Safety and Tolerance of Regadenoson in Subjects With Renal Impairment
NCT01101698PHASE4UNKNOWNVitamin K2 and Vessel Calcification in Chronic Kidney Disease Patients
NCT01150201PHASE4COMPLETEDAliskiren Combined With Losartan in Proteinuric, Non-diabetic Chronic Kidney Disease
NCT01155141PHASE4COMPLETEDIdiopathic Focal Segmental Glomerulosclerosis (FSGS) and Treatment With ACTH
NCT01228279PHASE4COMPLETEDSympathetic Activity in Patients With End-stage Renal Disease on Peritoneal Dialysis
NCT01437943PHASE4TERMINATEDEffect of Short Term Aliskiren Treatment in Kidney Transplant Patients
NCT01722513PHASE4UNKNOWNEfficacy and Safety of Alprostadil Prevent Contrast Induced Nephropathy
NCT01985360PHASE4COMPLETEDISCHEMIA-Chronic Kidney Disease Trial
NCT02311010PHASE4UNKNOWNPractical Use of Advagraf de Novo After Kidney Transplantation According to Recipient Genetic Polymorphism
NCT02413073PHASE4COMPLETEDWhole Body Vibration in Kidney Disease
NCT02444013PHASE4UNKNOWNFolic Acid for Prevention of Contrast Induced Nephropathy
NCT02707809PHASE4COMPLETEDEffects of Dexmedetomidine on Microcirculation of Kidney Transplant Recipient
NCT02761577PHASE4COMPLETEDA Prospective Study on Incidence and Prevention of Contrast-induced Nephropathy in Croatia
NCT03029351PHASE4TERMINATEDGLP-1 Receptor Agonist Therapy and Albuminuria in Patients With Type 2 Diabetes

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CINACALCET411
DARBEPOETIN ALFA48
LOSARTAN48
TACROLIMUS ANHYDROUS46
IOPAMIDOL44
LISINOPRIL ANHYDROUS44
ACETYLCYSTEINE43
ALEMTUZUMAB43
IOHEXOL43
LANTHANUM CARBONATE43
SIROLIMUS43
THEOPHYLLINE ANHYDROUS43
ALISKIREN42
CALCIUM42
CORTICOTROPIN42
DACLIZUMAB42
GLUCAGON42
NEDOSIRAN SODIUM42
PARICALCITOL42
REGADENOSON ANHYDROUS42
SODIUM BICARBONATE42
SPARSENTAN42
VADADUSTAT42
ACYCLOVIR41
ALLOPURINOL41
ALPROSTADIL41
ALTEPLASE41
ASCORBIC ACID41
BELATACEPT41
BREMELANOTIDE41