SE-ATLAS

Connectivite indifférenciée Néphropathie glomérulaire secondaire Maladie rénale associée à IgG4 Artérite à cellules géantes Lupus érythémateux disséminé de l'enfant Syndrome oculo-cérébro-rénal de Lowe Syndrome de Satoyoshi Syndrome de Joubert avec atteinte oculo-rénale Corticosurrénalome Sclérodermie systémique Polymyosite juvénile Pseudohypoaldostéronisme Cancer anaplasique de la thyroïde Syndrome de diabète insipide néphrogénique-calcifications intracrâniennes-petite taille-dysmorphie faciale Hyperparathyroïdie primitive sévère néonatale Cancer différencié de la thyroïde Vascularite secondaire Microangiopathie thrombotique Maladie systémique auto-immune Syndrome hémolytique et urémique atypique associé à une anomalie de MCP/CD 46 Syndrome hémolytique et urémique atypique associé à une anomalie C3 Néphropathie tubulaire génétique Syndrome hémolytique et urémique atypique associé à une anomalie du facteur H Artérite de Takayasu Syndrome hémolytique et urémique atypique associé à une anomalie du facteur B Hypercalciurie idiopathique Maladie de Dent Lupus érythémateux systémique autosomique Syndrome hémolytique et urémique atypique associé à des anticorps anti-facteur H Dysplasie cranio-ectodermique Atypical hemolytic uremic syndrome with I factor anomaly Senior-Loken syndrome Genetic primary hypomagnesemia Susac syndrome IgG4-related disease Shiga toxin-associated hemolytic uremic syndrome Genetic cystic renal disease Atypical hemolytic uremic syndrome with thrombomodulin anomaly Nail-patella syndrome Familial primary hyperparathyroidism Dominant hypophosphatemia with nephrolithiasis or osteoporosis Primary renal tubular acidosis Hypophosphatemic rickets Nephropathy secondary to a storage or other metabolic disease PLCG2-associated antibody deficiency and immune dysregulation Simple cryoglobulinemia VIPoma Nephrogenic syndrome of inappropriate antidiuresis Familial papillary thyroid carcinoma with renal papillary neoplasia Relapsing polychondritis Cystinuria type B Cystinuria type A Polymyositis Genetic hyperparathyroidism Rare genetic cause of hypertension Mitochondrial DNA depletion syndrome, hepatocerebrorenal form Familial nonmedullary thyroid carcinoma Primary Fanconi renotubular syndrome Alström syndrome Multiple endocrine neoplasia type 4 Senior-Boichis syndrome Multiple endocrine neoplasia Multiple endocrine neoplasia type 2A Multiple endocrine neoplasia type 2B Jeune syndrome Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome Pseudohypoparathyroidism EAST syndrome Hemolytic uremic syndrome with DGKE deficiency Congenital renal artery stenosis IgG4-related retroperitoneal fibrosis Cystinuria Overlapping connective tissue disease Saldino-Mainzer syndrome Primary glomerular disease Antisynthetase syndrome RHYNS syndrome Gitelman syndrome ACTH-independent Cushing syndrome Cushing syndrome due to ectopic ACTH secretion Rare disease with adrenal Cushing syndrome as a major feature Cushing syndrome due to bilateral macronodular adrenocortical disease Adrenal Cushing syndrome Dermatomyositis HNF1B-related autosomal dominant tubulointerstitial kidney disease Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Unclassified vasculitis Cushing disease Reynolds syndrome Hypotonia-cystinuria type 1 syndrome Medullary thyroid carcinoma Multiple endocrine neoplasia type 1 Multiple endocrine neoplasia type 2 Juvenile dermatomyositis Nephronophthisis Syndromic multisystem autoimmune disease due to Itch deficiency Predominantly large-vessel vasculitis Bartter syndrome Vasculitis Predominantly small-vessel vasculitis Hereditary renal hypouricemia Predominantly medium-vessel vasculitis Rare thyroid carcinoma Sarcoidosis Behçet disease Tubulointerstitial nephritis and uveitis syndrome Endogenous Cushing syndrome REN-related autosomal dominant tubulointerstitial kidney disease ACTH-dependent Cushing syndrome Atypical hemolytic uremic syndrome Autoimmune interstitial lung disease-arthritis syndrome Microscopic polyangiitis Nephrogenic diabetes insipidus Secondary neonatal autoimmune disease Mixed connective tissue disease Sjögren-Larsson syndrome Glomerular disease Basement membrane disease Granulomatosis with polyangiitis STAT3-related early-onset multisystem autoimmune disease Prolactinoma Rare renal tubular disease Rare cause of hypertension