autosomal dominant progressive nephropathy with hypertension | Kisho | Kisho

autosomal dominant progressive nephropathy with hypertension

Rare Disease

MONDO:0008071

Also known as:

nephropathy-hypertensionRFH1nephritis, familial, without deafness or ocular defect

Genes

–

Clinical Trials

106 active

Newborn Screening

–

Patient Groups

–

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

How we create this content →

Last reviewed: Feb 2026

QC Validated

Evidence base: Developing

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This report reflects available clinical information. Some areas may remain under active research.(6 data sources · Data coverage: Limited)

Overview

autosomal dominant progressive nephropathy with hypertension is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Symptoms & Signs

This condition is characterized by an autosomal dominant inheritance pattern. Known synonyms include nephropathy-hypertension and familial renal failure. There are currently no orphan drugs under investigation for this condition.

Prognosis & Outlook

Patients and caregivers are encouraged to seek genetic counseling to understand the implications of this inherited condition. Connecting with rare disease registries and online patient communities may provide additional support and resources.

Quick Resources

Helpful links for rare disease information and support

GARD (Genetic and Rare Diseases Information Center)NORD (National Organization for Rare Disorders)

General Questions to Consider

Questions that may be helpful when speaking with your healthcare team

•Are there specialists or centers of excellence with experience in this condition?
•Is there a patient registry I could participate in?
•What clinical trials might be available for this condition?
•Are there patient advocacy groups I should connect with?

This report reflects available clinical information. Some areas may remain under active research.(6 data sources · Data coverage: Limited)

Overview

autosomal dominant progressive nephropathy with hypertension is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Symptoms & Signs

Prognosis & Outlook

Quick Resources

Helpful links for rare disease information and support

GARD (Genetic and Rare Diseases Information Center)NORD (National Organization for Rare Disorders)

General Questions to Consider

Questions that may be helpful when speaking with your healthcare team

•Are there specialists or centers of excellence with experience in this condition?
•Is there a patient registry I could participate in?
•What clinical trials might be available for this condition?
•Are there patient advocacy groups I should connect with?

Overview

This report reflects available clinical information. Some areas may remain under active research.(6 data sources · Data coverage: Limited)

Overview

autosomal dominant progressive nephropathy with hypertension is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Symptoms & Signs

Prognosis & Outlook

Quick Resources

Helpful links for rare disease information and support

GARD (Genetic and Rare Diseases Information Center)NORD (National Organization for Rare Disorders)

General Questions to Consider

Questions that may be helpful when speaking with your healthcare team

•Are there specialists or centers of excellence with experience in this condition?
•Is there a patient registry I could participate in?
•What clinical trials might be available for this condition?
•Are there patient advocacy groups I should connect with?

Clinical

Inheritance Pattern

Autosomal Dominant

Inheritance patterns describe how genetic conditions are passed from parents to children.

Treatment

Clinical Trials

Research studies investigating treatments and therapies for this condition.

106

Active Trials

486

Total Trials

Filter trials on ClinicalTrials.gov:

View Recruiting Trials View All Trials

Data from ClinicalTrials.gov Jan 31, 2026

Support

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

Know a Patient Advocacy Group for this condition?

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AI-Generated Content: This summary was generated using AI. Content has been fact-checked. Always consult with qualified healthcare providers for medical guidance.

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autosomal dominant progressive nephropathy with hypertension

Patient-Friendly Information

Overview

Symptoms & Signs

Prognosis & Outlook

Quick Resources

General Questions to Consider

Overview

Symptoms & Signs

Prognosis & Outlook

Quick Resources

General Questions to Consider

Overview

Overview

Symptoms & Signs

Prognosis & Outlook

Quick Resources

General Questions to Consider

Clinical

Inheritance Pattern

Treatment

Clinical Trials

Support

External Resources

OMIM

Orphanet

GARD

Related Diseases

Know a Patient Advocacy Group for this condition?

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