SE-ATLAS

Primary interstitial lung disease in childhood and adulthood due to alveolar structure disorder 16q24.1 microdeletion syndrome Acute lung injury Primary interstitial lung disease specific to childhood Primary interstitial lung disease in childhood and adulthood due to alveolar vascular disorder Pigeon-breeder lung disease Bleeding disorder in hemophilia A carriers House allergic alveolitis Allergic bronchopulmonary aspergillosis Bleeding disorder in hemophilia B carriers Meconium aspiration syndrome Infant acute respiratory distress syndrome Tracheobronchopathia osteochondroplastica Hereditary angioedema type 2 Hereditary angioedema type 1 Infantile apnea Primary interstitial lung disease specific to childhood due to alveolar structure disorder Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies Congenital alveolar capillary dysplasia Acquired angioedema type 2 Renin-angiotensin-aldosterone system-blocker-induced angioedema Secondary interstitial lung disease in childhood and adulthood associated with a systemic disease Acquired angioedema type 1 Von Willebrand disease Isolated pulmonary capillaritis Von Willebrand disease type 2 Von Willebrand disease type 1 Idiopathic pulmonary hemosiderosis Secondary pulmonary hemosiderosis Staphylococcal necrotizing pneumonia Congenital chylothorax Von Willebrand disease type 2A Congenital pulmonary lymphangiectasia Heiner syndrome Sickle cell anemia Secondary interstitial lung disease specific to childhood associated with a systemic disease Hypersensitivity pneumonitis Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome Secondary interstitial lung disease in childhood and adulthood associated with a systemic vasculitis Combined pulmonary fibrosis-emphysema syndrome Idiopathic interstitial pneumonia Interstitial lung disease specific to infancy Secondary interstitial lung disease in childhood and adulthood associated with a metabolic disease Von Willebrand disease type 2B Drug or radiation exposure-related interstitial lung disease Von Willebrand disease type 2M Secondary interstitial lung disease specific to childhood associated with a systemic vasculitis Primary ciliary dyskinesia Primary ciliary dyskinesia-retinitis pigmentosa syndrome Secondary interstitial lung disease specific to childhood associated with a connective tissue disease Von Willebrand disease type 3 Secondary interstitial lung disease specific to childhood associated with a granulomatous disease Non-histaminic angioedema Chronic pneumonitis of infancy Sarcoidosis Hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies syndrome Severe hemophilia B Rare allergic respiratory disease Idiopathic pulmonary fibrosis Moderate hemophilia B Secondary interstitial lung disease specific to childhood associated with a metabolic disease Severe hemophilia A Mild hemophilia B Hemophilia A Moderate hemophilia A Hereditary angioedema Mild hemophilia A Severe acute respiratory syndrome Apnea of prematurity Neuroendocrine cell hyperplasia of infancy Pulmonary nodular lymphoid hyperplasia Secondary interstitial lung disease specific to adulthood associated with a systemic disease Pulmonary alveolar microlithiasis Interstitial lung disease Pulmonary interstitial glycogenosis Sudden infant death-dysgenesis of the testes syndrome Neonatal acute respiratory distress due to SP-B deficiency Recurrent respiratory papillomatosis Acute interstitial pneumonia Pneumonie, eosinophile idiopathische Pneumonie, interstitielle, lymphoide Bronchiektasie, idiopathische Chronische Atemnot mit Stoffwechseldefekt des Surfactant-Systems Pneumopathie, eosinophile idiopathische, chronische Spontanpneumothorax, familiärer Hämophilie Hämorrhagie, alveoläre diffuse Ataxia-Teleangiectasia Knorpel-Haar-Hypoplasie Lymphohistiozytose, hämophagozytische, primäre Granulomatose, chronische Infantile chronisch-entzündliche Darmerkrankung mit neurologischer Beteiligung X-chromosomale retikuläre Pigmentierungsstörung Glutaryl-CoA-Dehydrogenase-Mangel Mittelketten-Acyl-CoA-Dehydrogenase-Mangel Beta-Ketothiolase-Mangel Acyl-CoA-Dehydrogenase-Mangel, multipler Sehr langkettige-Acyl-CoA-Dehydrogenase-Mangel Methylmalonazidämie durch Methylmalonyl-CoA-Epimerase-Mangel Multipler Acyl-CoA-Dehydrogenase-Mangel, milder Typ Fruktose-1,6-Bisphosphatase-Mangel Glykogenose Typ 3 Homocystinurie, klassische Phenylketonurie, milde Phenylketonurie, klassische Glykogenose Typ 1a Phenylketonurie Methylmalonazidämie mit Homocystinurie Typ cbl D Lysinurische Proteinintoleranz (LPI) Methylmalonazidämie ohne Homocystinurie Ahornsirup-Krankheit Tyrosinämie Typ 1 Methylmalonazidämie, Vitamin B12-sensible Methylmalonazidämie mit Homocystinurie Typ cbl C Propionazidämie Multipler Acyl-CoA-Dehydrogenase-Mangel, schwerer neonataler Typ Langketten-3-Hydroxyacyl-CoA-Dehydrogenase-Mangel Methylmalonazidämie, Vitamin B12-resistente Siegler-Brewer-Carey-Syndrom Interstitielle Lungenkrankheit, spezifische, der Kindheit Interstitielle Lungenkrankheit, primäre, des Kindes/Erwachsenen Von-Willebrand-Syndrom Typ 2N Angioödem, erworbenes Hämophilie B Pneumonie, kryptogene organisierende Organoazidopathie, klassische Harnstoffzyklusdefekt und Störung der Ammoniak-Entgiftung Glykogenose Typ 1b Interstitielle Lungenkrankheit durch alveoläre Vaskulationsstörungen, primäre spezifische, der Kindheit Interstitielle Lungenkrankheit, sekundäre, des Kindes/Erwachsenen Sekundäre interstitielle Lungenkrankheit im Kindes- und Erwachsenenalter mit assoziierter Bindegewebsstörung Hereditäre fibröse Poikilodermie-Sehnenkontraktur-Myopathie-Lungenfibrose-Syndrom Jodmangelsyndrom, fetales Alopezie mit Antikörper-Mangel Phenylketonurie, maternale