Disease Directory Adult-onset myasthenia gravis
Neuromuscular

Adult-onset myasthenia gravis

Type

Clinical subtype

Gene

TNFRSF11A, CTLA4, HLA-DQA1

About Adult-onset myasthenia gravis

Adult-onset myasthenia gravis is a rare disease catalogued by Orphanet (ORPHA:391490). It is associated with the TNFRSF11A, CTLA4, HLA-DQA1 genes. 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 Adult-onset myasthenia gravis trials.

Search ClinicalTrials.gov for "Adult-onset myasthenia gravis" or filter by Orphanet code ORPHA:391490 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:391490)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Adult-onset myasthenia gravis trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Adult-onset myasthenia gravis. Updated daily.