Disease Directory Lujan-Fryns syndrome
Rare Disease

Lujan-Fryns syndrome

Type

Malformation syndrome

Gene

MED12, ZDHHC9, UPF3B

About Lujan-Fryns syndrome

Lujan-Fryns syndrome is a rare disease catalogued by Orphanet (ORPHA:776). It is associated with the MED12, ZDHHC9, UPF3B 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 Lujan-Fryns syndrome trials.

Search ClinicalTrials.gov for "Lujan-Fryns syndrome" or filter by Orphanet code ORPHA:776 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:776)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Lujan-Fryns syndrome trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Lujan-Fryns syndrome. Updated daily.