The Genetic Disorders of Mucociliary Clearance Consortium
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The Disorders We Study:

+ Primary Ciliary Dyskinesia (PCD)

+ Cystic Fibrosis

+ Pseudohypoaldosteronism (PHA)

+ Other Chronic Sinopulmonary Disease

Glossary of Terms

Frequently Asked Questions

Links and Resources

Take Action

How Can I help? - Why your participation matters

Join the Contact Registry

Learn about Current Research Studies

Find Support or Advocacy Groups

For Physicians

Learn More About Rare Mucociliary Clearance Diseases

Links and Resources

Participating Clinical Centers

New! Download: GDMCC Contact Registry Paper Form

Headlines

October North American Cystic Fibrosis, Orlando, FL
October 11-13, 2012
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WRAL.com: Diagnosing rare lung disorder is key to treatment
Although as many as 25,000 people in the United States live every day with primary ciliary dyskinesia, a chronic lung problem, only as estimated 10 percent are properly diagnosed. Read Article >