Disease Directory Nodular fasciitis
Rare Disease

Nodular fasciitis

Type

Disease

Gene

USP6, MYH9

About Nodular fasciitis

Nodular fasciitis is a rare disease catalogued by Orphanet (ORPHA:477742). It is associated with the USP6, MYH9 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 Nodular fasciitis trials.

Search ClinicalTrials.gov for "Nodular fasciitis" or filter by Orphanet code ORPHA:477742 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:477742)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Nodular fasciitis trials

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