About X-linked Alport syndrome-diffuse leiomyomatosis
X-linked Alport syndrome-diffuse leiomyomatosis is a rare disease catalogued by Orphanet (ORPHA:1018). It is associated with the COL4A6, COL4A5 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 X-linked Alport syndrome-diffuse leiomyomatosis trials.
Search ClinicalTrials.gov for "X-linked Alport syndrome-diffuse leiomyomatosis" or filter by Orphanet code ORPHA:1018 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 X-linked Alport syndrome-diffuse leiomyomatosis trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for X-linked Alport syndrome-diffuse leiomyomatosis. Updated daily.