Disease Directory Angiomatoid fibrous histiocytoma
Rare Disease

Angiomatoid fibrous histiocytoma

Type

Disease

Gene

CREB1, EWSR1

About Angiomatoid fibrous histiocytoma

Angiomatoid fibrous histiocytoma is a rare disease catalogued by Orphanet (ORPHA:569164). It is associated with the CREB1, EWSR1 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 Angiomatoid fibrous histiocytoma trials.

Search ClinicalTrials.gov for "Angiomatoid fibrous histiocytoma" or filter by Orphanet code ORPHA:569164 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:569164)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Angiomatoid fibrous histiocytoma trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Angiomatoid fibrous histiocytoma. Updated daily.