Disease Directory RELA fusion-positive ependymoma
Rare Disease

RELA fusion-positive ependymoma

Type

Disease

Gene

ZFTA, RELA

About RELA fusion-positive ependymoma

RELA fusion-positive ependymoma is a rare disease catalogued by Orphanet (ORPHA:530792). It is associated with the ZFTA, RELA 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 RELA fusion-positive ependymoma trials.

Search ClinicalTrials.gov for "RELA fusion-positive ependymoma" or filter by Orphanet code ORPHA:530792 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:530792)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting RELA fusion-positive ependymoma trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for RELA fusion-positive ependymoma. Updated daily.