Disease Directory Congenital alveolar capillary dysplasia
Respiratory

Congenital alveolar capillary dysplasia

Type

Disease

Gene

FOXF1

About Congenital alveolar capillary dysplasia

Congenital alveolar capillary dysplasia is a rare disease catalogued by Orphanet (ORPHA:210122). It is associated with the FOXF1 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 Congenital alveolar capillary dysplasia trials.

Search ClinicalTrials.gov for "Congenital alveolar capillary dysplasia" or filter by Orphanet code ORPHA:210122 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:210122)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Congenital alveolar capillary dysplasia trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Congenital alveolar capillary dysplasia. Updated daily.