Disease Directory Hemimegalencephaly
Rare Disease

Hemimegalencephaly

Type

Malformation syndrome

Gene

PIK3CA, AKT3, MTOR

About Hemimegalencephaly

Hemimegalencephaly is a rare disease catalogued by Orphanet (ORPHA:99802). It is associated with the PIK3CA, AKT3, MTOR 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 Hemimegalencephaly trials.

Search ClinicalTrials.gov for "Hemimegalencephaly" or filter by Orphanet code ORPHA:99802 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:99802)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Hemimegalencephaly trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Hemimegalencephaly. Updated daily.