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:
Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Autoimmune interstitial lung disease-arthritis syndrome Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Bardet-Biedl syndrome Bartter syndrome Biotinidase deficiency Bleeding disorder in hemophilia A carriers Bleeding disorder in hemophilia B carriers C3 glomerulonephritis CREST syndrome Carbamoyl-phosphate synthetase 1 deficiency Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Citrullinemia Cystic fibrosis Cystinosis Dent disease Denys-Drash syndrome Diffuse cutaneous systemic sclerosis Enthesitis-related juvenile idiopathic arthritis Eosinophilic fasciitis Fabry disease Galactosemia Gaucher disease Genetic steroid-resistant nephrotic syndrome Glycogen storage disease Hemophilia Hemophilia A Hemophilia B Idiopathic steroid-resistant nephrotic syndrome Idiopathic steroid-sensitive nephrotic syndrome Immunoglobulin A vasculitis Jeune syndrome Juvenile dermatomyositis Juvenile idiopathic arthritis Juvenile polymyositis Limited systemic sclerosis Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Maple syrup urine disease Medium chain acyl-CoA dehydrogenase deficiency Mild hemophilia A Mild hemophilia B Mixed connective tissue disease Moderate hemophilia A Moderate hemophilia B Motor neuron disease Mucolipidosis Mucopolysaccharidosis Multicystic dysplastic kidney Muscular channelopathy Neonatal dermatomyositis Neonatal lupus erythematosus Neonatal scleroderma Neuromuscular disease Neuromuscular junction disease Oligoarticular juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Ornithine transcarbamylase deficiency Osteochondrosis Overlapping connective tissue disease PLCG2-associated antibody deficiency and immune dysregulation Pediatric Castleman disease Pediatric systemic lupus erythematosus Phenylketonuria Polyarticular juvenile idiopathic arthritis Primary membranoproliferative glomerulonephritis Propionic acidemia Psoriasis-related juvenile idiopathic arthritis Rare hypercholesterolemia Rare pediatric systemic disease Renal dysplasia Renal hypoplasia Renal or urinary tract malformation Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis STAT3-related early-onset multisystem autoimmune disease Sarcoidosis Secondary neonatal autoimmune disease Severe hemophilia A Severe hemophilia B Short chain acyl-CoA dehydrogenase deficiency Skeletal muscle disease Systemic lupus erythematosus Systemic sclerosis Systemic-onset juvenile idiopathic arthritis Tubulointerstitial nephritis and uveitis syndrome Unexplained long-lasting fever/inflammatory syndrome Unspecified juvenile idiopathic arthritis Very long chain acyl-CoA dehydrogenase deficiency Waardenburg syndrome