About HSD10 disease, infantile type
HSD10 disease, infantile type is a rare disease catalogued by Orphanet (ORPHA:391428). It is associated with the HSD17B10 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 HSD10 disease, infantile type trials.
Search ClinicalTrials.gov for "HSD10 disease, infantile type" or filter by Orphanet code ORPHA:391428 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 HSD10 disease, infantile type trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for HSD10 disease, infantile type. Updated daily.