Disease Directory Giant axonal neuropathy
Rare Disease

Giant axonal neuropathy

Type

Disease

Gene

GAN

About Giant axonal neuropathy

Giant axonal neuropathy is a rare disease catalogued by Orphanet (ORPHA:643). It is associated with the GAN 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 Giant axonal neuropathy trials.

Search ClinicalTrials.gov for "Giant axonal neuropathy" or filter by Orphanet code ORPHA:643 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

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:643)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Giant axonal neuropathy trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Giant axonal neuropathy. Updated daily.