About Hereditary renal hypouricemia
Hereditary renal hypouricemia is a rare disease catalogued by Orphanet (ORPHA:94088). It is associated with the SLC22A12, SLC2A9 genes. 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 renal hypouricemia trials.
Search ClinicalTrials.gov for "Hereditary renal hypouricemia" or filter by Orphanet code ORPHA:94088 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 renal hypouricemia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Hereditary renal hypouricemia. Updated daily.