About KDM5C-related syndromic X-linked intellectual disability
KDM5C-related syndromic X-linked intellectual disability is a rare disease catalogued by Orphanet (ORPHA:85279). It is associated with the KDM5C gene. 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 KDM5C-related syndromic X-linked intellectual disability trials.
Search ClinicalTrials.gov for "KDM5C-related syndromic X-linked intellectual disability" or filter by Orphanet code ORPHA:85279 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
Find recruiting KDM5C-related syndromic X-linked intellectual disability trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for KDM5C-related syndromic X-linked intellectual disability. Updated daily.