Disease Directory X-linked intellectual disability, Wilson type
Rare Disease

X-linked intellectual disability, Wilson type

Type

Malformation syndrome

About X-linked intellectual disability, Wilson type

X-linked intellectual disability, Wilson type is a rare disease catalogued by Orphanet (ORPHA:85290). 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 X-linked intellectual disability, Wilson type trials.

Search ClinicalTrials.gov for "X-linked intellectual disability, Wilson type" or Orphanet code ORPHA:85290 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:85290)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting X-linked intellectual disability, Wilson type trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for X-linked intellectual disability, Wilson type. Updated daily.