Disease Directory Familial prostate cancer
Rare Disease

Familial prostate cancer

Type

Disease

Gene

CDH1, MSMB, RAD51D, ATM, SRD5A2, RNASEL

About Familial prostate cancer

Familial prostate cancer is a rare disease catalogued by Orphanet (ORPHA:1331). It is associated with the CDH1, MSMB, RAD51D genes. 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 Familial prostate cancer trials.

Search ClinicalTrials.gov for "Familial prostate cancer" or filter by Orphanet code ORPHA:1331 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:1331)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Familial prostate cancer trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial prostate cancer. Updated daily.