About GM3 synthase deficiency
GM3 synthase deficiency is a rare disease catalogued by Orphanet (ORPHA:370933). It is associated with the ST3GAL5 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 GM3 synthase deficiency trials.
Search ClinicalTrials.gov for "GM3 synthase deficiency" or filter by Orphanet code ORPHA:370933 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 GM3 synthase deficiency trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for GM3 synthase deficiency. Updated daily.