Disease Directory Takenouchi-Kosaki syndrome
Rare Disease

Takenouchi-Kosaki syndrome

Type

Malformation syndrome

Gene

CDC42

About Takenouchi-Kosaki syndrome

Takenouchi-Kosaki syndrome is a rare disease catalogued by Orphanet (ORPHA:487796). It is associated with the CDC42 gene. 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 Takenouchi-Kosaki syndrome trials.

Search ClinicalTrials.gov for "Takenouchi-Kosaki syndrome" or filter by Orphanet code ORPHA:487796 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:487796)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Takenouchi-Kosaki syndrome trials

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