About Hao-Fountain syndrome due to 16p13.2 microdeletion
Hao-Fountain syndrome due to 16p13.2 microdeletion is a rare disease catalogued by Orphanet (ORPHA:500055). It is associated with the USP7 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 Hao-Fountain syndrome due to 16p13.2 microdeletion trials.
Search ClinicalTrials.gov for "Hao-Fountain syndrome due to 16p13.2 microdeletion" or filter by Orphanet code ORPHA:500055 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 Hao-Fountain syndrome due to 16p13.2 microdeletion trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Hao-Fountain syndrome due to 16p13.2 microdeletion. Updated daily.