About X-linked intellectual disability with isolated growth hormone deficiency
X-linked intellectual disability with isolated growth hormone deficiency is a rare disease catalogued by Orphanet (ORPHA:67045). It is associated with the SOX3 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 X-linked intellectual disability with isolated growth hormone deficiency trials.
Search ClinicalTrials.gov for "X-linked intellectual disability with isolated growth hormone deficiency" or filter by Orphanet code ORPHA:67045 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 X-linked intellectual disability with isolated growth hormone deficiency trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for X-linked intellectual disability with isolated growth hormone deficiency. Updated daily.