Disease Directory Thrombomodulin-related bleeding disorder
Rare Disease

Thrombomodulin-related bleeding disorder

Type

Disease

Gene

THBD

About Thrombomodulin-related bleeding disorder

Thrombomodulin-related bleeding disorder is a rare disease catalogued by Orphanet (ORPHA:436169). It is associated with the THBD 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 Thrombomodulin-related bleeding disorder trials.

Search ClinicalTrials.gov for "Thrombomodulin-related bleeding disorder" or filter by Orphanet code ORPHA:436169 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:436169)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Thrombomodulin-related bleeding disorder trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Thrombomodulin-related bleeding disorder. Updated daily.