Congenital hydronephrosis

disease
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Summary

Congenital hydronephrosis (MONDO:0007741) is a disease and 6 clinical trials. Top therapeutic interventions include etomidate, midazolam, and propofol. A subtype of hydronephrosis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 6

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namecongenital hydronephrosis
Mondo IDMONDO:0007741
Orphanet2190
ICD-10-CMQ62.0
ICD-11808343797
NCITC102979
SNOMED CT16297002
UMLSC0266316
MedGen78594
MedDRA10050975
Is cancer (heuristic)no

Data availability: 1 cell line.

Disease family

This is a subtype of hydronephrosis. 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 disorderurinary tract obstructionhydronephrosiscongenital hydronephrosis

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: 6.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified5
PHASE41

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02013986PHASE4UNKNOWNEffects of Etomidate on Postoperative Circadian Rhythm Changes of Salivary Cortisol in Children
NCT06921733Not specifiedRECRUITINGUltrasound Localization Microscopy in Patient With Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)
NCT07382570Not specifiedNOT_YET_RECRUITINGNatural Course of Congenital Hydronephrosis in Infants Aged 0-6 Months
NCT07581223Not specifiedNOT_YET_RECRUITINGIntegrating an AI-Driven Hydronephrosis Decision-Making Tool
NCT01330511Not specifiedCOMPLETEDSimplified Diagnostic Algorithm for Evaluation of Neonates With Prenatally Detected Hydronephrosis
NCT05087537Not specifiedUNKNOWNEffect of Concomitant Bladder Neck Incision and Urethral Valve Ablation on Surgical Re-intervention Rate for Patients With Posterior Urethral Valve

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
ETOMIDATE41
MIDAZOLAM41
PROPOFOL41
S-ETOMIDATE-11