Disease Directory Anaplastic oligodendroglioma
Blood

Anaplastic oligodendroglioma

Type

Disease

Gene

IDH2, POT1

About Anaplastic oligodendroglioma

Anaplastic oligodendroglioma is a rare disease catalogued by Orphanet (ORPHA:251630). It is associated with the IDH2, POT1 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 Anaplastic oligodendroglioma trials.

Search ClinicalTrials.gov for "Anaplastic oligodendroglioma" or filter by Orphanet code ORPHA:251630 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:251630)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Anaplastic oligodendroglioma trials

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