Disease Directory Renal agenesis, unilateral
Renal

Renal agenesis, unilateral

Type

Clinical subtype

Gene

RET, FRAS1, BMP4, FREM2, FREM1, UPK3A

About Renal agenesis, unilateral

Renal agenesis, unilateral is a rare disease catalogued by Orphanet (ORPHA:93100). It is associated with the RET, FRAS1, BMP4 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 Renal agenesis, unilateral trials.

Search ClinicalTrials.gov for "Renal agenesis, unilateral" or filter by Orphanet code ORPHA:93100 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:93100)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Renal agenesis, unilateral trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Renal agenesis, unilateral. Updated daily.