Disease Directory OBSOLETE: Deletion 20p
Rare Disease

OBSOLETE: Deletion 20p

Type

Malformation syndrome

About OBSOLETE: Deletion 20p

OBSOLETE: Deletion 20p is a rare disease catalogued by Orphanet (ORPHA:1611). 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 OBSOLETE: Deletion 20p trials.

Search ClinicalTrials.gov for "OBSOLETE: Deletion 20p" or Orphanet code ORPHA:1611 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:1611)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting OBSOLETE: Deletion 20p trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for OBSOLETE: Deletion 20p. Updated daily.