Disease Directory Nephroblastoma
Renal

Nephroblastoma

Type

Disease

Gene

BRCA2, GPC3, CTR9, TRIM28, REST, TRIP13

About Nephroblastoma

Nephroblastoma is a rare disease catalogued by Orphanet (ORPHA:654). It is associated with the BRCA2, GPC3, CTR9 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 Nephroblastoma trials.

Search ClinicalTrials.gov for "Nephroblastoma" or filter by Orphanet code ORPHA:654 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:654)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Nephroblastoma trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Nephroblastoma. Updated daily.