SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


In the following you will find the diseases that are treated in this facility:
Alpha-1-antitrypsin deficiency Anorectal malformation Autoimmune interstitial lung disease-arthritis syndrome Autoinflammatory syndrome of childhood Bronchopulmonary dysplasia CINCA syndrome Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Chronic intestinal failure Chronic respiratory distress with surfactant metabolism deficiency Combined dystonia Congenital diaphragmatic hernia Cystic fibrosis Diaphragmatic or abdominal wall malformation Drug or radiation exposure-related interstitial lung disease Enthesitis-related juvenile idiopathic arthritis Exposure-related interstitial lung disease Familial Mediterranean fever Gastroschisis Glanzmann thrombasthenia Granulomatosis with polyangiitis Hemidystonia-hemiatrophy syndrome Hereditary spastic paraplegia Hyperimmunoglobulinemia D with periodic fever Hypersensitivity pneumonitis Idiopathic eosinophilic pneumonia Idiopathic pulmonary hemosiderosis Infantile dystonia-parkinsonism Infantile epileptic-dyskinetic encephalopathy Interstitial lung disease due to SP-C deficiency Interstitial lung disease in childhood and adulthood Interstitial lung disease specific to childhood Interstitial lung disease specific to infancy Isolated dystonia Juvenile idiopathic arthritis Langerhans cell histiocytosis specific to childhood Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome Lymphangioleiomyomatosis Mixed autoinflammatory and autoimmune syndrome Mixed connective tissue disease Non-syndromic anorectal malformation Oligoarticular juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Omphalocele Overlapping connective tissue disease Paroxysmal dyskinesia Paroxysmal dystonia Pediatric systemic lupus erythematosus Persistent combined dystonia Polyarticular juvenile idiopathic arthritis Primary ciliary dyskinesia Primary interstitial lung disease in childhood and adulthood Primary interstitial lung disease in childhood and adulthood due to alveolar structure disorder Primary interstitial lung disease in childhood and adulthood due to alveolar vascular disorder Primary interstitial lung disease specific to childhood Primary interstitial lung disease specific to childhood due to alveolar structure disorder Primary interstitial lung disease specific to childhood due to alveolar vascular disorder Psoriasis-related juvenile idiopathic arthritis Pyogenic autoinflammatory syndrome of childhood Rare disorder with dystonia and other neurologic or systemic manifestation Rare dystonia Rare endocrine growth disease Rare pediatric vasculitis Rare pulmonary hypertension Rare systemic or rheumatological disease of childhood Rare thyroid disease Reactive arthritis Rectal duplication Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Secondary interstitial lung disease in childhood and adulthood Secondary interstitial lung disease in childhood and adulthood associated with a systemic disease Secondary interstitial lung disease specific to childhood associated with a connective tissue disease Secondary interstitial lung disease specific to childhood associated with a granulomatous disease Secondary interstitial lung disease specific to childhood associated with a metabolic disease Secondary interstitial lung disease specific to childhood associated with a systemic disease Secondary interstitial lung disease specific to childhood associated with a systemic vasculitis Secondary neonatal autoimmune disease Secondary pulmonary alveolar proteinosis Secondary pulmonary hemosiderosis Syndromic anorectal malformation Systemic-onset juvenile idiopathic arthritis Unclassified autoinflammatory syndrome of childhood Unspecified juvenile idiopathic arthritis