SE-ATLAS

Acute lymphoblastic leukemia Acute myeloid leukemia Adrenogenital syndrome Alpha-1-antitrypsin deficiency Alpha-thalassemia Alport syndrome Anterior urethral valve Anti-neutrophil cytoplasmic antibody-associated vasculitis Astrocytoma Atypical hemolytic uremic syndrome Atypical teratoid rhabdoid tumor Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Beta-thalassemia C3 glomerulopathy Chondrosarcoma Citrullinemia type I Congenital hypogonadotropic hypogonadism Congenital hypothyroidism Congenital isolated ACTH deficiency Cyclic neutropenia Cystic fibrosis Dense deposit disease Dent disease Dent disease type 1 Ependymoma Extragonadal germinoma Familial peripheral male-limited precocious puberty Genetic tracheal anomaly Genetic transient congenital hypothyroidism Germinoma of the central nervous system Glioblastoma Glycine encephalopathy Glycogen storage disease due to phosphorylase kinase deficiency HNF1B-related autosomal dominant tubulointerstitial kidney disease Hemophagocytic syndrome associated with an infection Hemophilia Hepatoblastoma Hereditary chronic pancreatitis Hodgkin lymphoma Hypophosphatemic rickets Idiopathic nephrotic syndrome Immunoglobulin-mediated membranoproliferative glomerulonephritis Inflammatory myofibroblastic tumor Isolated congenital hypogonadotropic hypogonadism Isolated growth hormone deficiency type IA Isolated growth hormone deficiency type IB Isolated growth hormone deficiency type II Isolated growth hormone deficiency type III Ito hypomelanosis Juvenile xanthogranuloma Kostmann syndrome McCune-Albright syndrome Medium chain acyl-CoA dehydrogenase deficiency Medulloblastoma Myelodysplastic syndrome Nephroblastoma Nephrogenic diabetes insipidus Neuroblastoma Neuronal ceroid lipofuscinosis Non-Hodgkin lymphoma Non-acquired isolated growth hormone deficiency Non-syndromic renal or urinary tract malformation Ornithine transcarbamylase deficiency Osteosarcoma Pauci-immune glomerulonephritis Peripheral resistance to thyroid hormones Permanent congenital hypothyroidism Polyarteritis nodosa Polymicrogyria Pontocerebellar hypoplasia type 2 Posterior urethral valve Prader-Willi syndrome Predominantly large-vessel vasculitis Predominantly medium-vessel vasculitis Predominantly small-vessel vasculitis Primary biliary cholangitis Primary ciliary dyskinesia, Kartagener type Primary membranoproliferative glomerulonephritis Primary renal tubular acidosis Primary sclerosing cholangitis Pseudohypoparathyroidism Rapidly progressive glomerulonephritis Rare precocious puberty in female Renal or urinary tract malformation Rosaï-Dorfman disease Secondary vasculitis Septo-optic dysplasia spectrum Shiga toxin-associated hemolytic uremic syndrome Short bowel syndrome Short stature due to growth hormone qualitative anomaly Sickle cell anemia Skeletal Ewing sarcoma Testicular agenesis Thrombocytopenia-absent radius syndrome Transient congenital hypothyroidism Tubulointerstitial nephritis and uveitis syndrome Turner syndrome Unclassified vasculitis Undifferentiated connective tissue syndrome Vasculitis Yolk sac tumor