Disease Directory Familial adult myoclonic epilepsy
Neurological

Familial adult myoclonic epilepsy

Type

Disease

Gene

SAMD12, TNRC6A, RAPGEF2, YEATS2, CTNND2, CNTN2

About Familial adult myoclonic epilepsy

Familial adult myoclonic epilepsy is a rare disease catalogued by Orphanet (ORPHA:86814). It is associated with the SAMD12, TNRC6A, RAPGEF2 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 Familial adult myoclonic epilepsy trials.

Search ClinicalTrials.gov for "Familial adult myoclonic epilepsy" or filter by Orphanet code ORPHA:86814 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:86814)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Familial adult myoclonic epilepsy trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial adult myoclonic epilepsy. Updated daily.