SE-ATLAS

Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Bartter syndrome Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Cystic fibrosis Cystinosis Dent disease Denys-Drash syndrome Genetic steroid-resistant nephrotic syndrome 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 Maple syrup urine disease Periodic fever syndrome Phenylketonuria Primary membranoproliferative glomerulonephritis Psoriasis-related juvenile idiopathic arthritis Renal dysplasia Renal or urinary tract malformation Systemic lupus erythematosus Systemic sclerosis Tubulointerstitial nephritis and uveitis syndrome Tyrosinemia type 1 Tyrosinemia type 2 Tyrosinemia type 3 Vasculitis Waardenburg syndrome