About Hereditary folate malabsorption
Hereditary folate malabsorption is a rare disease catalogued by Orphanet (ORPHA:90045). It is associated with the SLC46A1 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 Hereditary folate malabsorption trials.
Search ClinicalTrials.gov for "Hereditary folate malabsorption" or filter by Orphanet code ORPHA:90045 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 Hereditary folate malabsorption trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Hereditary folate malabsorption. Updated daily.