Disease Directory Subcortical band heterotopia
Neurological

Subcortical band heterotopia

Type

Morphological anomaly

Gene

DCX, PAFAH1B1, EML1

About Subcortical band heterotopia

Subcortical band heterotopia is a rare disease catalogued by Orphanet (ORPHA:99796). It is associated with the DCX, PAFAH1B1, EML1 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 Subcortical band heterotopia trials.

Search ClinicalTrials.gov for "Subcortical band heterotopia" or filter by Orphanet code ORPHA:99796 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:99796)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Subcortical band heterotopia trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Subcortical band heterotopia. Updated daily.