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 interstitielle Pneumonie Scimitar-Syndrom Alpha-1-Antitrypsin-Mangel Pulmonale Alveolarproteinose, sekundäre Pulmonale Alveolarproteinose, autoimmune Bronchiektasie, idiopathische Pulmonale arterielle Hypertonie, hereditäre Pulmonale arterielle Hypertonie mit assoziierter Krankheit Pulmonale arterielle Hypertonie, Medikamenten- oder Toxin-induzierte Neuroendokrine Zellhyperplasie der Kindheit Pulmonale arterielle Hypertonie, idiopathische und/oder familiäre Pulmonale arterielle Hypertonie, idiopathische Lymphangioleiomyomatose Sarkoidose Pulmonale arterielle Hypertonie Interstitielle Lungenkrankheit Zilien-Dyskinesie, primäre