SE-ATLAS

HANAC-Syndrom Hyperkalzämie, infantile, autosomal-rezessive Bartter-Syndrom Typ 5 Liddle-Syndrom Reno-hepato-pankreatische Dysplasie Zahnschmelz-Niere-Syndrom Azidose, renale tubuläre, proximale, autosomal-dominante Form Kryoglobulinämische Vaskulitis Megazystis-Megaureter-Syndrom Azidose, renale tubuläre, proximale Alport-Syndrom Lupus erythematodes, systemischer Muckle-Wells-Syndrom Lipoprotein-Glomerulopathie Megaureter, primärer, adulte Form Nagel-Patella-Syndrom Megaureter, kongenitaler primärer, obstruktiver Form Megaureter, kongenitaler primärer, refluxierende Form Vesicoureteraler Reflux, familiäre Form Nierenagenesie Megaureter, kongenitaler primärer, nicht refluxierende und nicht obstruktive Formen Hämolytisch-urämisches Syndrom, atypische Form Aktionsmyoklonus-Nierenversagen-Syndrom Glomerulonephritis, membranoproliferative Alström-Syndrom Nephrotisches Syndrom, steroid-resistentes, genetisch bedingtes Hypotrichose - Lymphödem - Telangiektasie Dysgenesie, renale tubuläre, genetisch-bedingte Dominante Hypophosphatämie mit Nephrolithiasis oder Osteoporose Pierson-Syndrom Nephrotisches Syndrom, infantiles kongenitales Glomerulonephritis, primäre membranöse Interstitielle Lungenkrankheit-Nephrotisches Syndrom-Epidermolysis bullosa-Syndrom Kollagen Typ III-Glomerulopathie Glomerulonephritis, membranoproliferative, Typ 2 Azidose, renale tubuläre, mit Anämie Leigh-Syndrom mit nephrotischem Syndrom Denys-Drash-Syndrom Okulo-reno-zerebelläres Syndrom, schweres Fibronektin-Glomerulopathie Glomerulonephritis, membranoproliferative, Immunoglobulin-vermittelte Nephrotisches Syndrom, kongenitales, finnischer Typ Alport-Syndrom, X-chromosomales C3-Glomerulonephritis Idiopathisches Steroid-sensitives nephrotisches Syndrom mit sekundärer Steroid-Resistenz Frasier-Syndrom Idiopathisches steroid-resistentes nephrotisches Syndrom Idiopathisches MDR-resistentes nephrotisches Syndrom Idiopathisches steroid-resistentes nephrotisches Syndrom mit Sensitivität zu immunsuppressiver Zweitlinien-Therapie Familiäres steroidresistentes nephrotisches Syndrom mit Nebenniereninsuffizienz MYH9-assoziierte Krankheiten Nephrotisches Syndrom-Epidermolysis bullosa-sensorineurale Schwerhörigkeit-Syndrom Nephrotisches Syndrom, steroid-sensitives Kongenitale membranöse Nephropathie durch Alloimmunisierung gegen fetomaternale anti-neutrale Endopeptidase Knochendysplasie, immuno-ossäre, Typ Schimke Nephrotisches Syndrom, steroid-resistentes, mit sensorineuraler Hörstörung, familiäre Form Rachitis, hypophosphatämische, mit Hyperkalziurie Glomerulopathie, immunotaktoide oder fibrilläre Vaskulitis, hypokomplementämische urtikarielle Galloway-Mowat-Syndrom Charcot-Marie-Tooth-Krankheit, autosomal-dominante, intermediäre, Typ E Nierenhypoplasie, unilaterale Nierendysplasie, multizystische, unilaterale Form Okulo-zerebro-renales Syndrom Lowe Nierenhypoplasie, bilaterale De-novo thrombotische Mikroangiopathie nach Nierentransplantation Erworbenes monoklonales lg-Leichtketten-assoziiertes Fanconi-Syndrom Azidose, renale tubuläre, distale Alport-Syndrom, autosomal-rezessives Alport-Syndrom, autosomal-dominantes Nierendysplasie, multizystische, bilaterale Form Renale tubuläre Dysgenesie durch Zwilling-Zwilling-Transfusion Polymyositis, juvenile Atypisches hämolytisch-urämische Syndrom mit anti-Faktor H-Antikörpern Thrombotisch-thrombozytopenische Purpura, kongenitale Form Nephronophthise, spät beginnende Form Nephronophthise, infantile Form Hyperoxalurie, primäre, Typ 2 Hyperoxalurie, primäre, Typ 3 Xanthinurie Typ II Azidose, renale tubuläre, proximale, autosomal-rezessive Form Azidose, renale tubuläre, autosomal-dominante Form Zystinurie Typ B Zystinurie Typ A Hereditäre Amyloidose mit vorwiegender Nierenbeteiligung Renale Glukosurie, familiäre Dermatomyositis, juvenile Hämolytisch-urämisches Syndrom Atypisches hämolytisch-urämisches Syndrom mit Komplement-Gen-Anomalie Rachitis, hypophosphatämische, autosomal-dominante Hypophosphatämie, X-chromosomale Pseudohypoaldosteronismus, renaler, Typ 1 Hypotonie-Cystinurie-Syndrom Shiga-ähnliches Toxin-assoziiertes Hämolytisch-urämisches Syndrom Atresie des Urethers Behçet disease CREST syndrome Cystinuria Apparent mineralocorticoid excess Anti-glomerular basement membrane disease Familial hyperaldosteronism type I Primary hyperoxaluria Autosomal recessive distal renal tubular acidosis LCAT deficiency Autosomal dominant polycystic kidney disease Williams syndrome Autosomal dominant tubulointerstitial kidney disease Familial hyperaldosteronism type III Methylmalonic acidemia with homocystinuria, type cblC Renal coloboma syndrome Autoimmune interstitial lung disease-arthritis syndrome Senior-Boichis syndrome Idiopathic hypercalciuria Primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement Isolated autosomal dominant hypomagnesemia, Glaudemans type EAST syndrome MUC1-related autosomal dominant tubulointerstitial kidney disease IgG4-related kidney disease Prune belly syndrome Renal dysplasia HNF1B-related autosomal dominant tubulointerstitial kidney disease Primary hypomagnesemia-refractory seizures-intellectual disability syndrome Renal dysplasia, unilateral Drug-related renal tubular dysgenesis Phosphoribosylpyrophosphate synthetase superactivity Takayasu arteritis Genetic primary hypomagnesemia with hypocalciuria Genetic primary hypomagnesemia with normocalciuria Pediatric systemic lupus erythematosus ALys amyloidosis AFib amyloidosis Nephronophthisis Systemic sclerosis Genetic primary hypomagnesemia Bartter syndrome Osteopetrosis with renal tubular acidosis Hemolytic uremic syndrome with DGKE deficiency Primary hypomagnesemia with secondary hypocalcemia AApoAII amyloidosis Eosinophilic granulomatosis with polyangiitis Anterior urethral valve Brachydactyly-arterial hypertension syndrome AH amyloidosis Dermatomyositis Microscopic polyangiitis Oligomeganephronia Nephrogenic diabetes insipidus Idiopathic non-lupus full-house nephropathy Relapsing polychondritis Autosomal recessive polycystic kidney disease Polymyositis Pseudohypoaldosteronism type 1 REN-related autosomal dominant tubulointerstitial kidney disease Familial primary hypomagnesemia with normocalciuria and normocalcemia Autosomal dominant primary hypomagnesemia with hypocalciuria Oncogenic osteomalacia Renal agenesis, bilateral Renal agenesis, unilateral Isolated epispadias Infection-related hemolytic uremic syndrome Bladder exstrophy Generalized pseudohypoaldosteronism type 1 Pauci-immune glomerulonephritis with ANCA Hereditary renal hypouricemia Joubert syndrome with oculorenal defect Exstrophy-epispadias complex Pseudohypoaldosteronism type 2 Immunoglobulin A vasculitis Polyarteritis nodosa Medullary sponge kidney Reynolds syndrome Pauci-immune glomerulonephritis without ANCA Sarcoidosis Autosomal recessive hypophosphatemic rickets Familial Mediterranean fever Joubert syndrome with renal defect Mixed connective tissue disease Light and heavy chain deposition disease Tubulointerstitial nephritis and uveitis syndrome Heavy chain deposition disease Light chain deposition disease Thrombotic thrombocytopenic purpura Non-amyloid monoclonal immunoglobulin deposition disease Multicystic dysplastic kidney Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement AApoAI amyloidosis Dent disease Galactosemia Hereditary xanthinuria Von Hippel-Lindau disease Immune-mediated thrombotic thrombocytopenic purpura Juvenile nephronophthisis Gitelman syndrome Posterior urethral valve Giant cell arteritis Familial hyperaldosteronism type II Hypoxanthine-guanine phosphoribosyltransferase deficiency Primary hyperoxaluria type 1 Xanthinuria type I Buerger disease Pauci-immune glomerulonephritis Nephrogenic syndrome of inappropriate antidiuresis Granulomatosis with polyangiitis AApoAIV amyloidosis Dent disease type 2 Hypophosphatemic rickets Dent disease type 1 Congenital primary megaureter AL amyloidosis Familial hyperaldosteronism AA amyloidosis Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome Streptococcus pneumoniae-associated hemolytic uremic syndrome Mitochondrial oxidative phosphorylation disorder Cloacal exstrophy Renal tubular dysgenesis Renal dysplasia, bilateral Adenine phosphoribosyltransferase deficiency Diffuse cutaneous systemic sclerosis Fetal lower urinary tract obstruction Primary Fanconi renotubular syndrome Arthrogryposis-renal dysfunction-cholestasis syndrome Immunotactoid glomerulopathy Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis Non-amyloid fibrillary glomerulopathy UMOD-related autosomal dominant tubulointerstitial kidney disease Renal hypoplasia Congenital renal artery stenosis Primary systemic amyloidosis Primary localized amyloidosis