About Dowling-Degos disease
Dowling-Degos disease is a rare disease catalogued by Orphanet (ORPHA:79145). It is associated with the PSENEN, KRT5, POFUT1 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 Dowling-Degos disease trials.
Search ClinicalTrials.gov for "Dowling-Degos disease" or filter by Orphanet code ORPHA:79145 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
Find recruiting Dowling-Degos disease trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Dowling-Degos disease. Updated daily.