SE-ATLAS

Bartter-Syndrom Typ 5 Liddle-Syndrom Zahnschmelz-Niere-Syndrom Nagel-Patella-Syndrom Azidose, renale tubuläre, proximale Megaureter, kongenitaler primärer, refluxierende Form Nierenagenesie Megaureter, kongenitaler primärer, nicht refluxierende und nicht obstruktive Formen Alport-Syndrom Muckle-Wells-Syndrom Hämolytisch-urämisches Syndrom, atypische Form Lipoprotein-Glomerulopathie Aktionsmyoklonus-Nierenversagen-Syndrom Lupus erythematodes, systemischer Galloway-Mowat-Syndrom Azidose, renale tubuläre, distale Vaskulitis, hypokomplementämische urtikarielle Nierenhypoplasie, unilaterale Dominante Hypophosphatämie mit Nephrolithiasis oder Osteoporose Nierendysplasie, multizystische, unilaterale Form Nierenhypoplasie, bilaterale Nierendysplasie, multizystische, bilaterale Form Renale tubuläre Dysgenesie durch Zwilling-Zwilling-Transfusion Dysgenesie, renale tubuläre, Medikamenten-induzierte Hypotrichose-Lymphödem-Teleangiektasie-Nierenfunktionsstörung-Syndrom Atresie der Urethra Pierson-Syndrom Senior-Boichis-Syndrom Bartter-Syndrom Behçet-Syndrom Kollagen Typ III-Glomerulopathie Fibronektin-Glomerulopathie Azidose, renale tubuläre, distale, autosomal-rezessive Form LCAT-Mangel Nephronophthise Hyperkalziurie, idiopathische Hämolytisch-urämisches Syndrom mit DGKE-Mangel Phosphoribosylpyrophosphat-Synthetase-Überaktivität Okulo-reno-zerebelläres Syndrom, schweres Hypomagnesiämie, isolierte, autosomal-dominante, Typ Glaudemans Glomerulonephritis, membranoproliferative, Immunoglobulin-vermittelte EAST-Syndrom Systemische Sklerodermie CREST-Syndrom Autoimmune interstitielle Lungenkrankheit-Arthritis-Syndrom AApoAII-Amyloidose Hämolytisch-urämisches Syndrom C3-Glomerulonephritis Atypisches hämolytisch-urämisches Syndrom mit Komplement-Gen-Anomalie Zystinurie Takayasu-Arteriitis Nierenkrankheit, polyzystische, autosomal-dominante Denys-Drash-Syndrom Osteopetrose mit renaler tubulärer Azidose Idiopathisches Steroid-sensitives nephrotisches Syndrom mit sekundärer Steroid-Resistenz Idiopathisches steroid-resistentes nephrotisches Syndrom Idiopathisches MDR-resistentes nephrotisches Syndrom Idiopathisches steroid-resistentes nephrotisches Syndrom mit Sensitivität zu immunsuppressiver Zweitlinien-Therapie Nephrotisches Syndrom, infantiles kongenitales Glomerulonephritis, primäre membranöse MYH9-assoziierte syndromale Thrombozytopenie Knochendysplasie, immuno-ossäre, Typ Schimke Nephrotisches Syndrom-Epidermolysis bullosa-sensorineurale Schwerhörigkeit-Syndrom Apparenter Mineralocorticoid Exzess Familiäre Hypomagnesiämie mit Hyperkalziurie und Nephrokalzinose ohne schwere Augenbeteiligung Nephrotisches Syndrom, kongenitales, finnischer Typ Interstitielle Lungenkrankheit-Nephrotisches Syndrom-Epidermolysis bullosa-Syndrom Rachitis, hypophosphatämische, autosomal-dominante Hypophosphatämie, X-chromosomale Nephrotisches Syndrom, steroid-resistentes, mit sensorineuraler Hörstörung, familiäre Form Alport-Syndrom, X-chromosomales Alport-Syndrom, autosomal-rezessives Alport-Syndrom, autosomal-dominantes Hypotonie-Cystinurie-Syndrom Lupus erythematodes, systemischer, des Kindesalters IgG4-assoziierte Nierenkrankheit Antikörper vermittelte Krankheit der glomerulären Basalmembran AFib-Amyloidose Juvenile polymyositis Immunotactoid or fibrillary glomerulopathy Dense deposit disease Familial hyperaldosteronism type III Oculocerebrorenal syndrome of Lowe Atypical hemolytic uremic syndrome with anti-factor H antibodies Congenital thrombotic thrombocytopenic purpura Familial hyperaldosteronism type I Late-onset nephronophthisis Infantile nephronophthisis Prune belly syndrome Primary hyperoxaluria type 2 Methylmalonic acidemia with homocystinuria, type cblC Renal dysplasia Shiga toxin-associated hemolytic uremic syndrome Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Renal coloboma syndrome Idiopathic steroid-sensitive nephrotic syndrome Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization Hereditary amyloidosis with primary renal involvement Hereditary hypophosphatemic rickets with hypercalciuria Familial renal glucosuria Familial steroid-resistant nephrotic syndrome with adrenal insufficiency Primary hypomagnesemia-refractory seizures-intellectual disability syndrome Juvenile dermatomyositis Renal dysplasia, unilateral De novo thrombotic microangiopathy after kidney transplantation Frasier syndrome Renal pseudohypoaldosteronism type 1 Arthrogryposis-renal dysfunction-cholestasis syndrome Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement Fetal lower urinary tract obstruction Anterior urethral valve Eosinophilic granulomatosis with polyangiitis AH amyloidosis Oligomeganephronia Microscopic polyangiitis Relapsing polychondritis Autosomal recessive polycystic kidney disease Polymyositis Dermatomyositis Autosomal dominant primary hypomagnesemia with hypocalciuria Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome Streptococcus pneumoniae-associated hemolytic uremic syndrome Cloacal exstrophy Isolated epispadias Infection-related hemolytic uremic syndrome Diffuse cutaneous systemic sclerosis Bladder exstrophy Idiopathic non-lupus full-house nephropathy Pseudohypoaldosteronism type 1 Congenital primary megaureter Immunoglobulin A vasculitis Brachydactyly-arterial hypertension syndrome Polyarteritis nodosa Primary Fanconi renotubular syndrome Reynolds syndrome Joubert syndrome with oculorenal defect Oncogenic osteomalacia Pauci-immune glomerulonephritis with ANCA Medullary sponge kidney Pauci-immune glomerulonephritis without ANCA Sarcoidosis Immunotactoid glomerulopathy Mixed connective tissue disease Thrombotic thrombocytopenic purpura Renal agenesis, bilateral Multicystic dysplastic kidney Exstrophy-epispadias complex Primary systemic amyloidosis Primary localized amyloidosis Joubert syndrome with renal defect Familial Mediterranean fever Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis Generalized pseudohypoaldosteronism type 1 Gitelman syndrome Tubulointerstitial nephritis and uveitis syndrome Light and heavy chain deposition disease Heavy chain deposition disease Light chain deposition disease AApoAI amyloidosis Von Hippel-Lindau disease Granulomatosis with polyangiitis Congenital renal artery stenosis Hereditary renal hypouricemia Hereditary xanthinuria Immune-mediated thrombotic thrombocytopenic purpura Familial hyperaldosteronism type II Juvenile nephronophthisis Autosomal recessive hypophosphatemic rickets Hypophosphatemic rickets Dent disease type 2 Posterior urethral valve Dent disease type 1 AL amyloidosis AA amyloidosis AApoAIV amyloidosis Pauci-immune glomerulonephritis Adenine phosphoribosyltransferase deficiency Renal tubular dysgenesis Mitochondrial oxidative phosphorylation disorder Renal dysplasia, bilateral Non-amyloid monoclonal immunoglobulin deposition disease HANAC syndrome Primary megaureter, adult-onset form Alström syndrome Familial vesicoureteral reflux Acquired monoclonal Ig light chain-associated Fanconi syndrome Autosomal recessive infantile hypercalcemia Megacystis-megaureter syndrome Renal tubular dysgenesis of genetic origin Hypoxanthine-guanine phosphoribosyltransferase deficiency Dent disease Primary hypomagnesemia with secondary hypocalcemia Nephrogenic diabetes insipidus Non-amyloid fibrillary glomerulopathy ALys amyloidosis Primary hyperoxaluria type 1 Xanthinuria type I Buerger disease Familial hyperaldosteronism Cryoglobulinemic vasculitis Renal-hepatic-pancreatic dysplasia Primary membranoproliferative glomerulonephritis Genetic steroid-resistant nephrotic syndrome Pseudohypoaldosteronism type 2 Leigh syndrome with nephrotic syndrome Galactosemia Giant cell arteritis Primary hyperoxaluria Primary hyperoxaluria type 3 Xanthinuria type II Autosomal dominant proximal renal tubular acidosis Congenital primary megaureter, obstructed form Autosomal recessive proximal renal tubular acidosis Autosomal dominant distal renal tubular acidosis Cystinuria type B Cystinuria type A Nephrogenic syndrome of inappropriate antidiuresis Distal renal tubular acidosis with anemia Renal hypoplasia Renal agenesis, unilateral