About Hereditary motor and sensory neuropathy, Okinawa type
Hereditary motor and sensory neuropathy, Okinawa type is a rare disease catalogued by Orphanet (ORPHA:90117). It is associated with the TFG 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 Hereditary motor and sensory neuropathy, Okinawa type trials.
Search ClinicalTrials.gov for "Hereditary motor and sensory neuropathy, Okinawa type" or filter by Orphanet code ORPHA:90117 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 Hereditary motor and sensory neuropathy, Okinawa type trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Hereditary motor and sensory neuropathy, Okinawa type. Updated daily.