About Autosomal recessive intermediate Charcot-Marie-Tooth disease type C
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C is a rare disease catalogued by Orphanet (ORPHA:369867). It is associated with the PLEKHG5 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 Autosomal recessive intermediate Charcot-Marie-Tooth disease type C trials.
Search ClinicalTrials.gov for "Autosomal recessive intermediate Charcot-Marie-Tooth disease type C" or filter by Orphanet code ORPHA:369867 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 Autosomal recessive intermediate Charcot-Marie-Tooth disease type C trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Autosomal recessive intermediate Charcot-Marie-Tooth disease type C. Updated daily.