SE-ATLAS

Arthritis, idiopathische juvenile, Enthesitis-assoziierte Interstitielle Lungenkrankheit, primäre, des Kindes/Erwachsenen durch alveoläre Vaskulationsstörungen Autoinflammatorisches Syndrom, pyogenes, der Kindheit Interstitielle Lungenkrankheit, spezifische, der Kindheit Interstitielle Lungenkrankheit, primäre, des Kindes/Erwachsenen durch alveoläre Strukturanomlien Seltene systemische oder rheumatologische Krankheit der Kindheit Dyskinesie, paroxysmale Interstitielle Lungenkrankheit, sekundäre, des Kindes/Erwachsenen Schilddrüsenkrankheit, seltene Mittelmeerfieber, familiäres Interstitielle Lungenkrankheit, primäre spezifische, der Kindheit Hyperimmunglobulinämie D mit Rückfallfieber Autoinflammatorisches Syndrom, unklassifiziertes, der Kindheit Dysplasie, bronchopulmonale Mischkollagenose, überlappende Seltene Störung mit Dystonie und weiteren neurologischen oder systemischen Manifestationen Interstitielle Lungenkrankheit, sekundäre, des Kindes/Erwachsenen, mit assoziierter systemischer Krankheit CINCA-Syndrom Dystonie, paroxysmale Interstitielle Lungenkrankheit durch alveoläre Vaskulationsstörungen, primäre spezifische, der Kindheit Seltene Vaskulitis des Kindes Interstitielle Lungenkrankheit, spezifische, des Kleinkindes Lungen-Hämosiderose, sekundäre Arthritis, idiopathische juvenile Lungen-Hämosiderose, idiopathische Hypersensitivity pneumonitis Secondary interstitial lung disease specific to childhood associated with a connective tissue disease Drug or radiation exposure-related interstitial lung disease Secondary neonatal autoimmune disease Secondary interstitial lung disease specific to childhood associated with a systemic disease Exposure-related interstitial lung disease Primary ciliary dyskinesia Secondary interstitial lung disease specific to childhood associated with a granulomatous disease Secondary interstitial lung disease specific to childhood associated with a systemic vasculitis Interstitial lung disease due to SP-C deficiency Secondary interstitial lung disease specific to childhood associated with a metabolic disease Isolated dystonia Persistent combined dystonia Rare endocrine growth disease Mixed connective tissue disease Langerhans cell histiocytosis specific to childhood Lymphangioleiomyomatosis Autoimmune interstitial lung disease-arthritis syndrome Hemidystonia-hemiatrophy syndrome Syndromic anorectal malformation Combined dystonia Hereditary spastic paraplegia Autoinflammatory syndrome of childhood Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Interstitial lung disease in childhood and adulthood Chronic respiratory distress with surfactant metabolism deficiency Reactive arthritis Idiopathic eosinophilic pneumonia Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Unspecified juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis Glanzmann thrombasthenia Secondary pulmonary alveolar proteinosis Rare dystonia Polyarticular juvenile idiopathic arthritis Rectal duplication Mixed autoinflammatory and autoimmune syndrome Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Psoriasis-related juvenile idiopathic arthritis Chronic intestinal failure Infantile epileptic-dyskinetic encephalopathy Rare pulmonary hypertension Non-syndromic anorectal malformation Gastroschisis Anorectal malformation Pediatric systemic lupus erythematosus Granulomatosis with polyangiitis Omphalocele Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Primary interstitial lung disease specific to childhood due to alveolar structure disorder Diaphragmatic or abdominal wall malformation Infantile dystonia-parkinsonism Systemic-onset juvenile idiopathic arthritis Alpha-1-antitrypsin deficiency Primary interstitial lung disease in childhood and adulthood Congenital diaphragmatic hernia Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome