SE-ATLAS

HANAC syndrome Autosomal recessive infantile hypercalcemia Bartter syndrome type 5 Liddle syndrome Renal-hepatic-pancreatic dysplasia Enamel-renal syndrome Autosomal dominant proximal renal tubular acidosis Cryoglobulinemic vasculitis Megacystis-megaureter syndrome Proximal renal tubular acidosis Alport syndrome Systemic lupus erythematosus Muckle-Wells syndrome Lipoprotein glomerulopathy Primary megaureter, adult-onset form Nail-patella syndrome Congenital primary megaureter, obstructed form Congenital primary megaureter, refluxing form Familial vesicoureteral reflux Renal agenesis Congenital primary megaureter, nonrefluxing and unobstructed form Atypical hemolytic uremic syndrome Action myoclonus-renal failure syndrome Primary membranoproliferative glomerulonephritis Alström syndrome Genetic steroid-resistant nephrotic syndrome Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Renal tubular dysgenesis of genetic origin Dominant hypophosphatemia with nephrolithiasis or osteoporosis Pierson syndrome Congenital and infantile nephrotic syndrome Primary membranous glomerulonephritis Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome Collagen type III glomerulopathy Dense deposit disease Distal renal tubular acidosis with anemia Leigh syndrome with nephrotic syndrome Denys-Drash syndrome Severe oculo-renal-cerebellar syndrome Fibronectin glomerulopathy Immunoglobulin-mediated membranoproliferative glomerulonephritis Congenital nephrotic syndrome, Finnish type X-linked Alport syndrome C3 glomerulonephritis Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance Frasier syndrome Idiopathic steroid-resistant nephrotic syndrome Idiopathic multidrug-resistant nephrotic syndrome Idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunosuppressive therapy Familial steroid-resistant nephrotic syndrome with adrenal insufficiency MYH9-related disease Nephrotic syndrome-epidermolysis bullosa-sensorineural deafness syndrome Idiopathic steroid-sensitive nephrotic syndrome Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization Schimke immuno-osseous dysplasia Familial steroid-resistant nephrotic syndrome with sensorineural deafness Hereditary hypophosphatemic rickets with hypercalciuria Immunotactoid or fibrillary glomerulopathy Hypocomplementemic urticarial vasculitis Galloway-Mowat syndrome Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Renal hypoplasia, unilateral Unilateral multicystic dysplastic kidney Oculocerebrorenal syndrome of Lowe Renal hypoplasia, bilateral De novo thrombotic microangiopathy after kidney transplantation Acquired monoclonal Ig light chain-associated Fanconi syndrome Distal renal tubular acidosis Autosomal recessive Alport syndrome Autosomal dominant Alport syndrome Bilateral multicystic dysplastic kidney Renal tubular dysgenesis due to twin-twin transfusion Juvenile polymyositis Atypical hemolytic uremic syndrome with anti-factor H antibodies Congenital thrombotic thrombocytopenic purpura Late-onset nephronophthisis Infantile nephronophthisis Primary hyperoxaluria type 2 Primary hyperoxaluria type 3 Xanthinuria type II Autosomal recessive proximal renal tubular acidosis Autosomal dominant distal renal tubular acidosis Cystinuria type B Cystinuria type A Hereditary amyloidosis with primary renal involvement Familial renal glucosuria Juvenile dermatomyositis Hemolytic uremic syndrome Atypical hemolytic uremic syndrome with complement gene abnormality Autosomal dominant hypophosphatemic rickets X-linked hypophosphatemia Renal pseudohypoaldosteronism type 1 Hypotonia-cystinuria syndrome Shiga toxin-associated hemolytic uremic syndrome Atresia of urethra 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-Arteriitis Primäre Hypomagnesiämie mit Hypokalziurie, genetisch bedingte Hypomagnesiämie mit Normokalziurie, genetisch bedingte Lupus erythematodes, systemischer, des Kindesalters ALys-Amyloidose AFib-Amyloidose Nephronophthise Systemische Sklerodermie Hypomagnesiämie, primäre, genetisch bedingte Bartter-Syndrom Osteopetrose mit renaler tubulärer Azidose Hämolytisch-urämisches Syndrom mit DGKE-Mangel Primäre Hypomagnesiämie mit sekundärer Hypokalzämie AApoAII-Amyloidose Eosinophile Granulomatose mit Polyangiitis Anteriore Urethralklappen Brachydaktylie-arterielle Hypertension-Syndrom AH-Amyloidose Dermatomyositis Polyangiitis, mikroskopische Oligomeganephronie Diabetes insipidus, nephrogener Idiopathische non-Lupus Full-House-Nephropathie Polychondritis, rezidivierende Nierenkrankheit, polyzystische, autosomal-rezessive Polymyositis Pseudohypoaldosteronismus Typ 1 Nierenkrankheit, tubulointerstitielle, autosomal-dominante, REN-assoziierte Hypomagnesiämie, familiäre primäre, mit Normokalziurie und Normokalzämie Primäre Hypomagnesiämie mit Hypokalziurie, autosomal-dominant Osteomalazie, onkogene Nierenagenesie, bilaterale Nierenagenesie, unilaterale Epispadie, isolierte Infektions-assoziiertes hämolytisch-urämisches Syndrom Blasenekstrophie Pseudohypoaldosteronismus, generalisierter, Typ 1 Glomerulonephritis, pauci-immune, mit ANCA Hypourikämie, hereditäre renale Joubert-Syndrom mit okulo-renalem Defekt Ekstrophie-Epispadie-Komplex Pseudohypoaldosteronismus Typ 2 Immunoglobulin A-Vaskulitis Polyarteriitis nodosa Cacchi-Ricci-Syndrom Reynolds-Syndrom Glomerulonephritis, pauci-immune, ohne ANCA Sarkoidose Rachitis, hypophosphatämische, autosomal-rezessive Mittelmeerfieber, familiäres Joubert-Syndrom mit Nierenstörung Mischkollagenose Leichtketten- und Schwerketten-Speicherkrankheit Tubulointerstitielle Nephritis und Uveitis-Syndrom Schwerketten-Speicherkrankheit Leichtketten-Speicherkrankheit Purpura, thrombotische thrombozytopenische Nicht-amyloide monoklonale Immunglobulin-Ablagerungskrankheit Nierendysplasie, multizystische Primäre Hypomagnesiämie mit Hyperkalziurie, Nephrokalzinoseund schwerer Augenbeteiligung AApoAI-Amyloidose Dent-Krankheit Galaktosämie Xanthinurie, hereditäre Von-Hippel-Lindau-Krankheit Thrombotisch-thrombozytopenische Purpura, immun-vermittelte Nephronophthise, juvenile Form Gitelman-Syndrom Urethralklappen, posteriore Riesenzell-Arteriitis Hyperaldosteronismus, familiärer, Typ II Hypoxanthin-Guanin-Phosphoribosyltransferase-Mangel Hyperoxalurie, primäre, Typ 1 Xanthinurie Typ I Buerger-Krankheit Glomerulonephritis, pauci-immune Nephrogenes Syndrom mit unverhältnismäßiger Antidiurese Granulomatose mit Polyangiitis AApoAIV-Amyloidose Dent-Krankheit Typ 2 Hypophosphatämische Rachitis Dent-Krankheit Typ 1 Megaureter, kongenitaler primärer AL-Amyloidose Hyperaldosteronismus, familiärer AA-Amyloidose Hypohydrosis-Elektrolytstörung-Tränendrüsenfunktionsstörung-Ichthyosis-Xerostomie-Syndrom Streptococcus pneumoniae-assoziiertes hämolytisch-urämisches Syndrom Mitochondriale Störungen der oxidativen Phosphorylierung Kloakenekstrophie Dysgenesie, renale tubuläre Nierendysplasie, bilaterale Adenin-Phosphoribosyl-Transferase-Mangel Systemische Sklerose, diffuse kutane Fetale Obstruktion des Blasenhalses Renotubuläres Fanconi-Syndrom, primäres Arthrogrypose-Nierenfunktionsstörung-Cholestase-Syndrom Glomerulopathie, immunotaktoide Nierenkrankheit, polyzystische, autosomal-dominante, Typ 1, mit tuberöser Sklerose Glomerulopathie, fibrilläre nicht-amyloide Nierenerkrankung, tubulointerstitielle, autosomal-dominante, UMOD-assoziierte Nierenhypoplasie Nierenarterienstenose, kongenitale Amyloidose, primäre systemische Amyloidose, lokalisierte primäre