About Feingold syndrome type 2
Feingold syndrome type 2 is a rare disease catalogued by Orphanet (ORPHA:391646). It is associated with the MIR17HG 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 Feingold syndrome type 2 trials.
Search ClinicalTrials.gov for "Feingold syndrome type 2" or filter by Orphanet code ORPHA:391646 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 Feingold syndrome type 2 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Feingold syndrome type 2. Updated daily.