Disease Directory Unilateral multicystic dysplastic kidney
Renal

Unilateral multicystic dysplastic kidney

Type

Clinical subtype

Gene

HNF1B

About Unilateral multicystic dysplastic kidney

Unilateral multicystic dysplastic kidney is a rare disease catalogued by Orphanet (ORPHA:97363). 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 Unilateral multicystic dysplastic kidney trials.

Search ClinicalTrials.gov for "Unilateral multicystic dysplastic kidney" or filter by Orphanet code ORPHA:97363 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:97363)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Unilateral multicystic dysplastic kidney trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Unilateral multicystic dysplastic kidney. Updated daily.