Disease Directory Isochromosome Y syndrome
Rare Disease

Isochromosome Y syndrome

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Category

About Isochromosome Y syndrome

Isochromosome Y syndrome is a rare disease catalogued by Orphanet (ORPHA:96325). 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 worldwide.

Clinical Trial Eligibility Tips

What to know before applying to Isochromosome Y syndrome trials.

Search ClinicalTrials.gov for "Isochromosome Y syndrome" or Orphanet code ORPHA:96325 to find disease-specific recruiting studies.

Ask your specialist to refer you to an Orphanet-accredited Centre of Expertise for this condition.

Natural history studies and patient registries often open enrolment before drug trials — contact the Orphanet patient community first.

Patient Resources

Patient Organization

Orphanet

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Orphanet

European reference resource for rare diseases (ORPHA:96325)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Isochromosome Y syndrome trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Isochromosome Y syndrome. Updated daily.