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  2. Alpha-1 antitrypsin deficiency - Wikipedia

    en.wikipedia.org/wiki/Alpha-1_antitrypsin_deficiency

    Alpha-1 antitrypsin deficiency (A1AD or AATD) is a genetic disorder that may result in lung disease or liver disease. [1] Onset of lung problems is typically between 20 and 50 years of age. [1] This may result in shortness of breath, wheezing, or an increased risk of lung infections.

  3. Birt–Hogg–Dubé syndrome - Wikipedia

    en.wikipedia.org/wiki/Birt–Hogg–Dubé_syndrome

    Birt-Hogg-Dubé Syndrome patients, families, and caregivers are encouraged to join the NIH Rare Lung Diseases Consortium Contact Registry. This is a privacy-protected site that provides up-to-date information for individuals interested in the latest scientific news, trials, and treatments related to rare lung diseases.

  4. Cystic fibrosis - Wikipedia, the free encyclopedia

    en.wikipedia.org/wiki/Cystic_fibrosis

    Cystic fibrosis (also known as CF or mucoviscidosis) is an autosomal recessive genetic disorder affecting most critically the lungs, and also the pancreas, liver, and intestine.

  5. Alveolar capillary dysplasia - Wikipedia

    en.wikipedia.org/wiki/Alveolar_capillary_dysplasia

    ACD is a rare disease. As of 2011, about 100 cases had been reported. It is likely an under-recognized cause of death shortly after birth because diagnosis requires microscopic examination of lung tissue or specialized genetic testing, or death can be attributed to severe heart or intestinal congenital abnormalities which frequently occur in ...

  6. Congenital pulmonary airway malformation - Wikipedia

    en.wikipedia.org/wiki/Congenital_pulmonary...

    Congenital pulmonary airway malformation (CPAM), formerly known as congenital cystic adenomatoid malformation (CCAM), is a congenital disorder of the lung similar to bronchopulmonary sequestration. In CPAM, usually an entire lobe of lung is replaced by a non-working cystic piece of abnormal lung tissue.

  7. Pulmonary alveolar microlithiasis - Wikipedia

    en.wikipedia.org/wiki/Pulmonary_alveolar_micro...

    Pulmonary Alveolar Microlithiasis patients, families, and caregivers are encouraged to join the NIH Rare Lung Diseases Consortium Contact Registry. This is a privacy protected site that provides up-to-date information for individuals interested in the latest scientific news, trials, and treatments related to rare lung diseases. [citation needed]

  8. Primary ciliary dyskinesia - Wikipedia

    en.wikipedia.org/wiki/Primary_ciliary_dyskinesia

    Primary ciliary dyskinesia (PCD) is a rare, autosomal recessive genetic ciliopathy, that causes defects in the action of cilia lining the upper and lower respiratory tract, sinuses, Eustachian tube, middle ear, fallopian tube, and flagella of sperm cells.

  9. Category:Lung disorders - Wikipedia

    en.wikipedia.org/wiki/Category:Lung_disorders

    Pages in category "Lung disorders" The following 74 pages are in this category, out of 74 total. This list may not reflect recent changes. A. Acute eosinophilic ...

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