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 Idiopathic eosinophilic pneumonia Lymphoid interstitial pneumonia Idiopathic bronchiectasis Chronic respiratory distress with surfactant metabolism deficiency Idiopathic chronic eosinophilic pneumonia Familial spontaneous pneumothorax Hemophilia Diffuse alveolar hemorrhage Ataxia-telangiectasia Cartilage-hair hypoplasia Primary hemophagocytic lymphohistiocytosis Chronic granulomatous disease Infantile inflammatory bowel disease with neurological involvement X-linked reticulate pigmentary disorder Glutaryl-CoA dehydrogenase deficiency Medium chain acyl-CoA dehydrogenase deficiency Beta-ketothiolase deficiency Multiple acyl-CoA dehydrogenase deficiency Very long chain acyl-CoA dehydrogenase deficiency Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency Multiple acyl-CoA dehydrogenase deficiency, mild type Fructose-1,6-bisphosphatase deficiency Glycogen storage disease due to glycogen debranching enzyme deficiency Homocystinuria due to cystathionine beta-synthase deficiency Mild phenylketonuria Classic phenylketonuria Glycogen storage disease due to glucose-6-phosphatase deficiency type Ia Phenylketonuria Methylmalonic acidemia with homocystinuria, type cblD Lysinuric protein intolerance Methylmalonic acidemia without homocystinuria Maple syrup urine disease Tyrosinemia type 1 Vitamin B12-responsive methylmalonic acidemia Methylmalonic acidemia with homocystinuria, type cblC Propionic acidemia Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Vitamin B12-unresponsive methylmalonic acidemia Siegler-Brewer-Carey syndrome Interstitial lung disease specific to childhood Primary interstitial lung disease in childhood and adulthood Von Willebrand disease type 2N Acquired angioedema Hemophilia B Cryptogenic organizing pneumonia Classic organic aciduria Disorder of urea cycle metabolism and ammonia detoxification Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib Primary interstitial lung disease specific to childhood due to alveolar vascular disorder Secondary interstitial lung disease in childhood and adulthood Secondary interstitial lung disease in childhood and adulthood associated with a connective tissue disease Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome Fetal iodine syndrome Alopecia antibody deficiency Maternal phenylketonuria