Disease Directory Hereditary breast cancer
Rare Disease

Hereditary breast cancer

Type

Disease

Gene

NQO2, ATM, CDH1, BRCA1, BRCA2, PALB2

About Hereditary breast cancer

Hereditary breast cancer is a rare disease catalogued by Orphanet (ORPHA:227535). It is associated with the NQO2, ATM, CDH1 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 Hereditary breast cancer trials.

Search ClinicalTrials.gov for "Hereditary breast cancer" or filter by Orphanet code ORPHA:227535 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:227535)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Hereditary breast cancer trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Hereditary breast cancer. Updated daily.