Disease Directory Medullary sponge kidney
Renal

Medullary sponge kidney

Type

Morphological anomaly

Gene

HNF1B

About Medullary sponge kidney

Medullary sponge kidney is a rare disease catalogued by Orphanet (ORPHA:1309). It is associated with the HNF1B gene. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.

Clinical Trial Eligibility Tips

What to know before applying to Medullary sponge kidney trials.

Search ClinicalTrials.gov for "Medullary sponge kidney" or filter by Orphanet code ORPHA:1309 to find disease-specific studies.

Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.

Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.

Patient Resources

Patient Organization

Orphanet

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:1309)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Medullary sponge kidney trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Medullary sponge kidney. Updated daily.