Disease Directory Brachydactyly type A2
Rare Disease

Brachydactyly type A2

Type

Malformation syndrome

Gene

BMP2, GDF5, BMPR1B

About Brachydactyly type A2

Brachydactyly type A2 is a rare disease catalogued by Orphanet (ORPHA:93396). It is associated with the BMP2, GDF5, BMPR1B 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 Brachydactyly type A2 trials.

Search ClinicalTrials.gov for "Brachydactyly type A2" or filter by Orphanet code ORPHA:93396 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:93396)

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NORD

National Organization for Rare Disorders

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Find recruiting Brachydactyly type A2 trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Brachydactyly type A2. Updated daily.