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pseudohypoaldosteronism - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

pseudohypoaldosteronism

MONDO:0018638

Find Clinical TrialsTrials

Overview

An inherited or acquired disorder of electrolyte metabolism, characterized by the inability of the renal tubules to respond to aldosterone. It is manifested by hyperkalemic metabolic acidosis, urinary salt wasting, normal or increased aldosterone secretion and normal glomerular filtration rate.

Clinical Trials3 registered · 1 recruiting

Diagnosis

Biomarker and diagnostic research for pseudohypoaldosteronism has been reported in the published literature.

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.

3 clinical trials registered, 1 recruiting. Interventions under study include other interventions. Research is primarily sponsored by academic and government institutions.

63 publications have been identified in PubMed for pseudohypoaldosteronism. Research spans Case Report / Case Series (65%), Review / Meta-Analysis (17%), and Epidemiology / Natural History (8%).

Research Type	Count	% of Total
Patient case studies	41	65%

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 6:53 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:444916

GARD

Genetic and Rare Diseases Info Center

GARD:21861

Questions for Your Care Team

→Are any of the 3 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?

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pseudohypoaldosteronism

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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