Disease Directory OBSOLETE: Shoulder and girdle defects-familial intellectual disability syndrome
Rare Disease

OBSOLETE: Shoulder and girdle defects-familial intellectual disability syndrome

Type

Malformation syndrome

About OBSOLETE: Shoulder and girdle defects-familial intellectual disability syndrome

OBSOLETE: Shoulder and girdle defects-familial intellectual disability syndrome is a rare disease catalogued by Orphanet (ORPHA:2580). 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: Shoulder and girdle defects-familial intellectual disability syndrome trials.

Search ClinicalTrials.gov for "OBSOLETE: Shoulder and girdle defects-familial intellectual disability syndrome" or Orphanet code ORPHA:2580 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:2580)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting OBSOLETE: Shoulder and girdle defects-familial intellectual disability syndrome trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for OBSOLETE: Shoulder and girdle defects-familial intellectual disability syndrome. Updated daily.