Disease Directory Acrocapitofemoral dysplasia
Rare Disease

Acrocapitofemoral dysplasia

Type

Malformation syndrome

Gene

IHH

About Acrocapitofemoral dysplasia

Acrocapitofemoral dysplasia is a rare disease catalogued by Orphanet (ORPHA:63446). It is associated with the IHH 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 Acrocapitofemoral dysplasia trials.

Search ClinicalTrials.gov for "Acrocapitofemoral dysplasia" or filter by Orphanet code ORPHA:63446 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:63446)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Acrocapitofemoral dysplasia trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Acrocapitofemoral dysplasia. Updated daily.