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autosomal dominant progressive nephropathy with hypertension - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal dominant progressive nephropathy with hypertension

MONDO:0008071

Also known as:nephropathy-hypertensionRFH1nephritis, familial, without deafness or ocular defect

Find Clinical TrialsTrials

Overview

GeneticsAutosomal dominant

Clinical Trials1 registered · 1 recruiting

Clinical Presentation

Built from Human Phenotype Ontology (HPO) phenotype annotations and GeneReviews clinical descriptions. Features represent findings documented across known cases — not an exhaustive list of possible symptoms.

Features include: Stage 5 chronic kidney disease, Nephritis, Reduced kidney function (renal insufficiency), and Microscopic hematuria and 3 more.

Organ System	Phenotype Count	Example Features
Kidneys and urinary system	6	Stage 5 chronic kidney disease, Nephritis, Reduced kidney function (renal insufficiency)

Diagnosis

Biomarker and diagnostic research for autosomal dominant progressive nephropathy with hypertension has been reported in the published literature.

Prognosis

Estimated prevalence: <1 in 1,000,000 (VERY_RARE).

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.

1 clinical trial registered, 1 recruiting. Interventions under study include gene therapy. Research is primarily sponsored by academic and government institutions.

177 publications have been identified in PubMed for autosomal dominant progressive nephropathy with hypertension. Kisho has analyzed 91 by research type. Research spans Review / Meta-Analysis (41%), Case Report / Case Series (15%), and Basic Science / Preclinical (15%).

Research Type	Count	% of Total
Research summaries	37

Data assembled from 6 of 12 sources · Last updated Sep 19, 2026, 10:40 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:161900

Orphanet

European rare disease database

Orphanet:88659

GARD

Genetic and Rare Diseases Info Center

GARD:16772

Questions for Your Care Team

→Are any of the 1 active clinical trial 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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Kisho

autosomal dominant progressive nephropathy with hypertension

Overview

Clinical Presentation

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

OMIM

Orphanet

GARD

Questions for Your Care Team

Questions for Your Care Team

Explore clinical features

Recent Publications

autosomal dominant progressive nephropathy with hypertension

Overview

Clinical Presentation

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Explore clinical features

Recent Publications