Disease Directory Classic bladder exstrophy
Rare Disease

Classic bladder exstrophy

Type

Clinical subtype

Gene

TP63, ISL1

About Classic bladder exstrophy

Classic bladder exstrophy is a rare disease catalogued by Orphanet (ORPHA:93930). It is associated with the TP63, ISL1 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 Classic bladder exstrophy trials.

Search ClinicalTrials.gov for "Classic bladder exstrophy" or filter by Orphanet code ORPHA:93930 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

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:93930)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Classic bladder exstrophy trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Classic bladder exstrophy. Updated daily.