Disease Directory X-linked non-syndromic intellectual disability
Rare Disease

X-linked non-syndromic intellectual disability

Type

Etiological subtype

Gene

STEEP1, CASK, RPS6KA3, ARX, DMD, FTSJ1

About X-linked non-syndromic intellectual disability

X-linked non-syndromic intellectual disability is a rare disease catalogued by Orphanet (ORPHA:777). It is associated with the STEEP1, CASK, RPS6KA3 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 X-linked non-syndromic intellectual disability trials.

Search ClinicalTrials.gov for "X-linked non-syndromic intellectual disability" or filter by Orphanet code ORPHA:777 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

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Orphanet

European reference resource for rare diseases (ORPHA:777)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting X-linked non-syndromic intellectual disability trials

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