Idiopathic Pulmonary Fibrosis (IPF) is a frightening, incurable disease where the lungs become increasingly damaged by scar tissue, resulting in breathing getting progressively more difficult.

94010 (spirometry, including graphic record, total and timed vital capacity, expiratory flow rate measurement) 4,285 50.7 94014 (patient-initiated spirometric recording per 30-d period of time ...

Allergic bronchopulmonary aspergillosis is a pulmonary disease occurring in patients with asthma or cystic fibrosis, consequent to a dysregulated immune response to inhaled Aspergillus conidia.