A comprehensive DNA test that screens 81 genes for inherited respiratory disorders including cystic fibrosis, ciliary dyskinesia, pulmonary fibrosis, and emphysema.


Cystic fibrosis & airway clearance
Genes behind cystic fibrosis and CF-like conditions that cause thick mucus buildup in the lungs and airways.
Primary ciliary dyskinesia
Genes needed for the tiny hair-like cilia that sweep mucus out of the lungs. Defects cause chronic infections, bronchiectasis, and sometimes reversed organ placement.
Pulmonary fibrosis & scarring
Genes linked to inherited pulmonary fibrosis, where lung tissue progressively scars. Telomere genes are the most common familial cause.
Surfactant & newborn lung disease
Genes essential for surfactant, the coating that keeps air sacs open. Defects can cause severe breathing problems in newborns or lung disease later in life.
Pulmonary hypertension
Genes that cause dangerously high blood pressure in the lung arteries. BMPR2 is the most commonly inherited cause of pulmonary arterial hypertension.
Alpha-1 antitrypsin & emphysema
Genes that protect lung tissue from breakdown. Alpha-1 antitrypsin deficiency is one of the most common inherited causes of early emphysema and COPD.
Lung cysts & deposits
Genes linked to lung cysts or nodules that may increase the risk of collapsed lung (pneumothorax).
Hermansky-Pudlak syndrome
Genes behind Hermansky-Pudlak syndrome, a rare condition causing lung fibrosis, easy bruising, and light skin/eye color.
Breathing control & nerve signaling
Genes controlling the signals that drive breathing. PHOX2B changes cause congenital central hypoventilation, where automatic breathing fails during sleep.
Know your genetic risks. Share with your doctor. Breathe easier with a plan.