SE-ATLAS

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