Disease Directory Autosomal dominant spastic ataxia type 1
Neurological

Autosomal dominant spastic ataxia type 1

Type

Disease

Gene

VAMP1

About Autosomal dominant spastic ataxia type 1

Autosomal dominant spastic ataxia type 1 is a rare disease catalogued by Orphanet (ORPHA:251282). It is associated with the VAMP1 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 dominant spastic ataxia type 1 trials.

Search ClinicalTrials.gov for "Autosomal dominant spastic ataxia type 1" or filter by Orphanet code ORPHA:251282 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

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Orphanet

European reference resource for rare diseases (ORPHA:251282)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Autosomal dominant spastic ataxia type 1 trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Autosomal dominant spastic ataxia type 1. Updated daily.