Disease Directory Hereditary papillary renal cell carcinoma
Renal

Hereditary papillary renal cell carcinoma

Type

Disease

Gene

MET

About Hereditary papillary renal cell carcinoma

Hereditary papillary renal cell carcinoma is a rare disease catalogued by Orphanet (ORPHA:47044). It is associated with the MET 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 Hereditary papillary renal cell carcinoma trials.

Search ClinicalTrials.gov for "Hereditary papillary renal cell carcinoma" or filter by Orphanet code ORPHA:47044 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:47044)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Hereditary papillary renal cell carcinoma trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Hereditary papillary renal cell carcinoma. Updated daily.