Disease Directory Hereditary renal hypouricemia
Renal

Hereditary renal hypouricemia

Type

Malformation syndrome

Gene

SLC22A12, SLC2A9

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

Patient Organization

Orphanet

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Orphanet

European reference resource for rare diseases (ORPHA:94088)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Hereditary renal hypouricemia trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Hereditary renal hypouricemia. Updated daily.