Disease Directory Classic pyoderma gangrenosum
Rare Disease

Classic pyoderma gangrenosum

Type

Clinical subtype

Gene

PTPN6

About Classic pyoderma gangrenosum

Classic pyoderma gangrenosum is a rare disease catalogued by Orphanet (ORPHA:538863). It is associated with the PTPN6 gene. 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 Classic pyoderma gangrenosum trials.

Search ClinicalTrials.gov for "Classic pyoderma gangrenosum" or filter by Orphanet code ORPHA:538863 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:538863)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Classic pyoderma gangrenosum trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Classic pyoderma gangrenosum. Updated daily.