SE-ATLAS

Glomerulonephritis, membranoproliferative, nicht Immunoglobulin-vermittelte Glomerulopathie Albright-Osteodystrophie, hereditäre Nieren/Harnwegsfehlbildung, syndromale Glomerulopathie, sekundäre Vaskulitis mit assoziierten antineutrophilen zytoplasmatischen Antikörpern Dysgenesie, renale tubuläre, Medikamenten-induzierte Basalmembrandefekt Methylcobalamin-Mangel Typ cbl G Lupus erythematodes, systemischer, des Kindesalters HANAC-Syndrom Sebastian-Syndrom Okulo-zerebro-renales Syndrom Lowe Osteofibröse Dysplasie Nephrotisches Syndrom, steroid-resistentes, mit sensorineuraler Hörstörung, familiäre Form Alport-Syndrom, X-chromosomales Mischkollagenose AApoAII-Amyloidose Hyperaldosteronismus, familiärer, Typ I Nephrotisches Syndrom-Epidermolysis bullosa-sensorineurale Schwerhörigkeit-Syndrom Nierenkrankheit, polyzystische, autosomal-dominante, Typ 1, mit tuberöser Sklerose ALys-Amyloidose Vaskulitis, hypokomplementämische urtikarielle AApoAI-Amyloidose Ziliopathie mit vorwiegend skelettaler Beteiligung AFib-Amyloidose Smith-Lemli-Opitz-Syndrom Dysplasie, metaphysäre Hypertension durch 'gain-of-function'-Mutationen im Mineralocorticoid-Rezeptor C3-Glomerulonephritis Langketten-3-Hydroxyacyl-CoA-Dehydrogenase-Mangel Nephropathie, progressive mit Hypertension, autosomal-dominante Form Dysplasie, akromele Hyperoxalurie, primäre Glomerulonephritis, membranoproliferative, Typ 2 Nephrogener Diabetes insipidus-intrakranielle Kalzifikation-Kleinwuchs-Gesichtsdysmorphie-Syndrom Hydronephrose, kongenitale Dysplasie, spondylodysplastische Tyrosinämie Typ 2 Dysplasie, mesomele und rhizo-mesomele Dysplasie, akromesomele Pseudohypoaldosteronismus, transienter Vaskulitis durch ADA2-Mangel Vaskulitis, sekundäre Pseudohypoaldosteronismus Typ 2B Mikroangiopathie, thrombotische Atypisches hämolytisch-urämische Syndrom mit MCP- oder CD46-Anomalie Kampomele Dysplasie und verwandte Krankheiten Pseudohypoaldosteronismus Typ 2A Neugeborenen-Diabetes - kongenitale Hypothyreose - kongenitales Glaukom - Leberfibrose - polyzystische Nieren Atypisches hämolytisch-urämische Syndrom mit C3-Anomalie Arthritis, idiopathische juvenile, oligoartikuläre, mit anti-nukleären Antikörpern Chondrodysplasia punctata Primäre Hypomagnesiämie mit Hyperkalziurie, Nephrokalzinoseund schwerer Augenbeteiligung Primäre Knochendysplasie mit multiplen Gelenkdislokationen Pseudohypoaldosteronismus Typ 2C Atypisches hämolytisch-urämische Syndrom mit B-Faktor-Anomalie Hyperkalziurie, idiopathische Hyperthyreose durch TSH-Rezeptor-Genmutationen, familiäre Form Dent-Krankheit Atypisches hämolytisch-urämische Syndrom mit I-Faktor-Anomalie Primäre Knochendysplasie mit erhöhter Knochendichte Atypisches hämolytisch-urämische Syndrom mit H-Faktor-Anomalie Glomerulonephritis, rapid-progressive Thrombotisch-thrombozytopenische Purpura, kongenitale Form Nierendysplasie, bilaterale Primäre Knochendysplasie mit erniedrigter Knochendichte Azidose, renale tubuläre, distale Hypotonie-Cystinurie-Syndrom Nierendysplasie, unilaterale Phaeochromozytom, sporadisches Galloway-Mowat-Syndrom Arthritis, reaktive Thrombotisch-thrombozytopenische Purpura, immun-vermittelte Carnitin-Palmitoyl-Transferase IA-Mangel Megakalikose, kongenitale, unilaterale Hypomagnesiämie, primäre, genetisch bedingte Carnitin-Palmitoyl-Transferase II-Mangel Hypomagnesiämie, familiäre primäre, mit Normokalziurie und Normokalzämie Nephrotisches Syndrom, kongenitales, finnischer Typ Phäochromozytom-Paragangliom-Syndrom, hereditäres Shiga-ähnliches Toxin-assoziiertes Hämolytisch-urämisches Syndrom Pseudohypoaldosteronismus, renaler, Typ 1 Zystische Nierenerkrankung, genetisch bedingte Atypisches hämolytisch-urämische Syndrom mit Thrombomodulin-Anomalie Adenin-Phosphoribosyl-Transferase-Mangel Primäre Hypomagnesiämie mit Hypokalziurie, autosomal-dominant Kleidokraniale Dysplasie und isolierten kranialen Ossifikationsdefekt Primäre Knochendysplasie mit desorganisierter Skelettentwicklung Pseudohypoaldosteronismus, generalisierter, Typ 1 Mikrodeletionssyndrom 2p21 Nierenerkrankung, tubulointerstitielle, autosomal-dominante, UMOD-assoziierte Carnitin-Mangel, primärer systemischer Nagel-Patella-Syndrom Osteolyse, primäre Nierenerkrankung, tubulointerstitielle, autosomal-dominante, MUC1-assoziierte Megakalikose, kongenitale, bilaterale Arthritis, idiopathische juvenile, oligoartikuläre, ohne anti-nukleäre Antikörper Sporadisches Phaeochromozytom/sezernierendes Paragangliom Hyperlipidämie, seltene Nephronophthise, spät beginnende Form Nephrotisches Syndrom, idiopathisches Glutaryl-CoA-Dehydrogenase-Mangel Arthritis, idiopathische juvenile polyartikuläre, Rheumafaktor-negative Erworbenes monoklonales lg-Leichtketten-assoziiertes Fanconi-Syndrom Methylmalonic acidemia with homocystinuria Dominant hypophosphatemia with nephrolithiasis or osteoporosis Tyrosinemia type 3 Infantile nephronophthisis Primary renal tubular acidosis Oligoarticular juvenile idiopathic arthritis Immunotactoid or fibrillary glomerulopathy Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome Action myoclonus-renal failure syndrome Juvenile nephronophthisis Unspecified juvenile idiopathic arthritis Bickerstaff brainstem encephalitis NPHP3-related Meckel-like syndrome May-Hegglin thrombocytopenia Primary hyperoxaluria type 1 Renal tubular dysgenesis Phenylketonuria Sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy Primary hyperoxaluria type 3 Rare inborn errors of metabolism Catecholamine-producing tumor Lysosomal disease Primary hyperoxaluria type 2 Xanthinuria type II Lethal chondrodysplasia Xanthinuria type I Congenital and infantile nephrotic syndrome Antenatal Bartter syndrome Rare renal tubular disease Short stature-advanced bone age-early-onset osteoarthritis syndrome Cystic fibrosis Nephrogenic syndrome of inappropriate antidiuresis Medium chain acyl-CoA dehydrogenase deficiency Primary membranous glomerulonephritis Bartter syndrome type 3 Peroxisomal disease Autosomal dominant distal renal tubular acidosis Genetic primary hypomagnesemia with hypocalciuria Autosomal recessive proximal renal tubular acidosis Thrombotic thrombocytopenic purpura Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation Autosomal recessive distal renal tubular acidosis without deafness Apparent mineralocorticoid excess Brachydactyly-arterial hypertension syndrome Autosomal recessive distal renal tubular acidosis with deafness Idiopathic steroid-sensitive nephrotic syndrome Autosomal recessive polycystic kidney disease Primary hypomagnesemia with hypercalciuria and nephrocalcinosis Exstrophy-epispadias complex Polyarticular juvenile idiopathic arthritis Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization Cystinuria type B Idiopathic steroid-sensitive nephrotic syndrome with minimal change Autosomal dominant tubulointerstitial kidney disease Pseudohypoaldosteronism type 2D Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Rare systemic or rheumatological disease of childhood Idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation Rare genetic cause of hypertension Isolated autosomal dominant hypomagnesemia, Glaudemans type REN-related autosomal dominant tubulointerstitial kidney disease Bartter syndrome type 4 Enthesitis-related juvenile idiopathic arthritis Schimke immuno-osseous dysplasia Genetic primary hypomagnesemia with normocalciuria Disorder of fatty acid oxidation and ketogenesis Psoriasis-related juvenile idiopathic arthritis Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation Hereditary xanthinuria Kosaki overgrowth syndrome Osteopetrosis with renal tubular acidosis Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis Multiple acyl-CoA dehydrogenase deficiency Very long chain acyl-CoA dehydrogenase deficiency Hereditary fructose intolerance Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes Disorder of urea cycle metabolism and ammonia detoxification Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis Disorder of carnitine cycle and carnitine transport Alport syndrome Rare renal disease X-linked Alport syndrome-diffuse leiomyomatosis Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis Mitochondrial trifunctional protein deficiency Primary Fanconi renotubular syndrome Pseudohypoaldosteronism type 2E Tyrosinemia type 1 Pseudopseudohypoparathyroidism Epstein syndrome Senior-Boichis syndrome Pseudohypoparathyroidism type 1C Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes Hereditary amyloidosis with primary renal involvement Hemolytic uremic syndrome with DGKE deficiency Congenital primary megaureter Collagen type III glomerulopathy Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome Pseudohypoparathyroidism Pseudohypoaldosteronism type 1 Fechtner syndrome Adult familial nephronophthisis-spastic quadriparesia syndrome Frasier syndrome WAGR syndrome Pseudohypoaldosteronism type 2 Renal agenesis, bilateral Cystinosis Pseudoxanthoma elasticum Congenital renal artery stenosis Cystinuria Overlapping connective tissue disease Oligomeganephronia Dent disease type 1 Multicystic dysplastic kidney Renal-hepatic-pancreatic dysplasia Pierson syndrome Urachal cyst Galactosemia Primary glomerular disease Renal hypoplasia Medullary sponge kidney RHYNS syndrome Primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement Renal agenesis, unilateral Denys-Drash syndrome Megacystis-megaureter syndrome Primary membranoproliferative glomerulonephritis Gitelman syndrome Williams syndrome Nephrogenic diabetes insipidus Atypical hemolytic uremic syndrome Rare pediatric vasculitis Congenital megacalycosis Posterior urethral valve Bladder exstrophy Primary bone dysplasia Juvenile idiopathic arthritis Cloacal exstrophy Rare pediatric systemic disease Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Glycogen storage disease Unclassified vasculitis Primary bone dysplasia with micromelia Primary megaureter, adult-onset form Primary bone dysplasia with progressive ossification of skin, skeletal muscle, fascia, tendons and ligaments Primary hypomagnesemia with secondary hypocalcemia Lipoprotein glomerulopathy Duplication of urethra Multiple paragangliomas associated with polycythemia Maple syrup urine disease Congenital primary megaureter, nonrefluxing and unobstructed form Anti-glomerular basement membrane disease Hypotonia-cystinuria type 1 syndrome MYH9-related disease Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome Immunoglobulin-mediated membranoproliferative glomerulonephritis Atresia of urethra Juvenile dermatomyositis Otopalatodigital syndrome spectrum disorder Glutaric acidemia type 3 Nephronophthisis Genetic steroid-resistant nephrotic syndrome Hereditary renal hypouricemia Atypical hypotonia-cystinuria syndrome Pseudohypoparathyroidism type 2 Unilateral multicystic dysplastic kidney Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia Renal hypoplasia, bilateral Liddle syndrome Spondylometaphyseal dysplasia Tubulointerstitial nephritis and uveitis syndrome Non-syndromic renal or urinary tract malformation Disorder of purine or pyrimidine metabolism Familial juvenile hyperuricemic nephropathy type 1 Bilateral multicystic dysplastic kidney Sporadic idiopathic steroid-resistant nephrotic syndrome Renal or urinary tract malformation Familial gestational hyperthyroidism Methylmalonic acidemia without homocystinuria Autosomal dominant proximal renal tubular acidosis Idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis Isovaleric acidemia Propionic acidemia Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies Nail-patella-like renal disease Congenital primary megaureter, obstructed form Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies Proximal renal tubular acidosis Congenital primary megaureter, refluxing form Renal hypoplasia, unilateral Pseudohypoparathyroidism type 1A Senior-Loken syndrome Renal tubular dysgenesis due to twin-twin transfusion Renal tubular dysgenesis of genetic origin Bartter syndrome Fibronectin glomerulopathy Ochoa syndrome Sporadic secreting paraganglioma Carnitine-acylcarnitine translocase deficiency Megacystis-microcolon-intestinal hypoperistalsis syndrome Isolated epispadias Multiple epiphyseal dysplasia and pseudoachondroplasia Bartter syndrome with hypocalcemia Slender bone dysplasia Primary bone dysplasia with defective bone mineralization Joubert syndrome with oculorenal defect Rare infectious disease LAMB2-related infantile-onset nephrotic syndrome Autosomal recessive Alport syndrome Autosomal dominant Alport syndrome Von Hippel-Lindau disease Pseudohypoparathyroidism type 1B Atypical hemolytic uremic syndrome with anti-factor H antibodies Prune belly syndrome Systemic-onset juvenile idiopathic arthritis Distal renal tubular acidosis with anemia Cystinuria type A Rare cause of hypertension Renal dysplasia Dent disease type 2 Renal coloboma syndrome Pauci-immune glomerulonephritis Adrenocortical carcinoma