Kisho

Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy

idiopathic nephrotic syndrome - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

idiopathic nephrotic syndrome

MONDO:0018170

Find Clinical TrialsTrials

Overview

Nephrotic syndrome for which no cause has been identified.

Clinical Trials9 registered · 4 recruiting

Diagnosis

Biomarker and diagnostic research for idiopathic nephrotic syndrome 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.

9 clinical trials registered, 4 recruiting. Interventions under study include other interventions and drug therapy. Pipeline includes 1 PHASE4, 2 PHASE3. Research is sponsored by a mix of industry and academic institutions.

NCT ID	Title	Phase	Sponsor	Status
[NCT06635720](https://clinicaltrials.gov/study/NCT06635720)

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 6:55 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:357502

GARD

Genetic and Rare Diseases Info Center

GARD:21539

Questions for Your Care Team

→Are any of the 9 active clinical trials a good fit for my situation?
→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

← Back to All Diseases

Research Type	Count	% of Total
Clinical study results	38	24%
Laboratory research	35	22%
Disease patterns and progression	24	15%
Testing and diagnosis research	22	14%
Research summaries	16	10%
Patient case studies	12	8%
Other research	5	3%
New treatment approaches	4	3%

idiopathic nephrotic syndrome

Overview

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications