SE-ATLAS

Congenital lobar emphysema Cystic fibrosis Hereditary pulmonary alveolar proteinosis Congenital pulmonary airway malformation type 3 Idiopathic pulmonary fibrosis Combined pulmonary fibrosis-emphysema syndrome Congenital pulmonary airway malformation type 4 Interstitial lung disease due to ABCA3 deficiency Cryptogenic organizing pneumonia Acute interstitial pneumonia Congenital pulmonary airway malformation Congenital pulmonary sequestration Lymphoid interstitial pneumonia Chronic respiratory distress with surfactant metabolism deficiency Non-specific interstitial pneumonia Intralobar congenital pulmonary sequestration Williams-Campbell syndrome Congenital pulmonary lymphangiectasia Extralobar congenital pulmonary sequestration Primary pulmonary hypoplasia Communicating congenital bronchopulmonary-foregut malformation Pulmonary agenesis Autoimmune interstitial lung disease-arthritis syndrome Congenital pulmonary airway malformation type 0 Interstitial lung disease due to SP-C deficiency Congenital pulmonary airway malformation type 1 Congenital pulmonary airway malformation type 2 Desquamative interstitial pneumonia Scimitar syndrome Alpha-1-antitrypsin deficiency Secondary pulmonary alveolar proteinosis Autoimmune pulmonary alveolar proteinosis Idiopathic bronchiectasis Heritable pulmonary arterial hypertension Pulmonary arterial hypertension associated with another disease Drug- or toxin-induced pulmonary arterial hypertension Neuroendocrine cell hyperplasia of infancy Idiopathic/heritable pulmonary arterial hypertension Idiopathic pulmonary arterial hypertension Lymphangioleiomyomatosis Sarcoidosis Pulmonary arterial hypertension Interstitial lung disease Primary ciliary dyskinesia