SE-ATLAS

PAPA syndrome Renal-hepatic-pancreatic dysplasia HANAC syndrome Autosomal dominant proximal renal tubular acidosis Liddle syndrome Galloway-Mowat syndrome Distal renal tubular acidosis Idiopathic steroid-sensitive nephrotic syndrome with minimal change Oculocerebrorenal syndrome of Lowe Idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis Idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation Rare pediatric rheumatologic disease Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies Aicardi-Goutières syndrome Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies Renal agenesis Hypocomplementemic urticarial vasculitis NLRP12-associated hereditary periodic fever syndrome Muckle-Wells syndrome Alport syndrome Alström syndrome DITRA Nephrogenic diabetes insipidus-intracranial calcification-short stature-facial dysmorphism syndrome Vasculitis due to ADA2 deficiency Ventriculomegaly-cystic kidney disease Unilateral multicystic dysplastic kidney Juvenile idiopathic arthritis Behçet disease Neonatal inflammatory skin and bowel disease PFAPA syndrome STING-associated vasculopathy with onset in infancy Systemic sclerosis CREST syndrome Eosinophilic granulomatosis with polyangiitis Cherubism Autoimmune interstitial lung disease-arthritis syndrome Tumor necrosis factor receptor 1 associated periodic syndrome Sterile multifocal osteomyelitis with periostitis and pustulosis Takayasu arteritis Autoinflammatory syndrome of childhood Blau syndrome Diffuse cutaneous systemic sclerosis Limited cutaneous systemic sclerosis Limited systemic sclerosis Immunoglobulin A vasculitis NLRP3-associated autoinflammatory disease Vaskulitis, sekundäre Seltene systemische oder rheumatologische Krankheit der Kindheit Kawasaki-Krankheit Mevalonatkinase-Mangel Vaskulitis, postinfektiöse Hereditäres periodisches Fiebersyndrom Autoinflammatorisches Syndrom, pyogenes, der Kindheit Periodisches Fiebersyndrom der Kindheit Autoinflammatorisches Syndrom, granulomatöses, der Kindheit Mittelmeerfieber, familiäres Hyperimmunglobulinämie D mit Rückfallfieber Autoinflammatorisches Syndrom, unklassifiziertes, der Kindheit Chronische nicht-bakterielle Osteomyelitis/rezidivierende multifokale Osteomyelitis Unerklärliches periodisches Fierbersyndrom der Kindheit Lupus erythematodes, systemischer, des Kindesalters Proteasom-assoziiertes autoinflammatorisches Syndrom Chilblain-Lupus, familiärer Polymyositis, juvenile Granulomatose mit Polyangiitis USP18-Mangel CANDLE-Syndrom STAT3-assoziierte früh beginnende multisystemische Autoimmunkrankheit Arthritis, idiopathische juvenile polyartikuläre, Rheumafaktor-negative Arthritis, idiopathische juvenile, oligoartikuläre Arthritis, idiopathische juvenile, systemische CINCA-Syndrom Pannikulitis mit Uveitis und systemischer Granulomatose, infantile Form Mischkollagenose, überlappende Arthritis, idiopathische juvenile polyartikuläre, Rheumafaktor-positive Vaskulitis, Medikamenten-induzierte Arthritis, idiopathische juvenile, Enthesitis-assoziierte Periodisches Fieber-infantile Enterocolitis-autoinflammatorisches Syndrom Behçet-ähnliche Krankheit des Kindes, hereditäre Vaskulitis, unklassifizierte Kälte-Urtikaria, familiäre Fieber-Syndrom, langanhaltendes unerklärbares Dermatomyositis, juvenile Vaskulitis mit assoziierten antineutrophilen zytoplasmatischen Antikörpern Pseudohypoparathyreoidismus Typ 1A Senior-Loken-Syndrom Hypertension durch 'gain-of-function'-Mutationen im Mineralocorticoid-Rezeptor Nierendysplasie, multizystische, bilaterale Form Pseudohypoparathyreoidismus Typ 1C Hämolytisch-urämisches Syndrom, atypische Form Dysgenesie, renale tubuläre, genetisch-bedingte Adulte familiäre Nephronophthise-spastische Tetraparese-Syndrom BOR-Syndrom Pierson-Syndrom Bartter-Syndrom Senior-Boichis-Syndrom Dent-Krankheit Methylcobalamin-Mangel Typ cbl G Fibronektin-Glomerulopathie Azidose, renale tubuläre, distale, autosomal-rezessive Form Hydronephrose, kongenitale Nephrotisches Syndrom, steroid-resistentes, genetisch bedingtes Primäre Hypomagnesiämie mit Hyperkalziurie, Nephrokalzinoseund schwerer Augenbeteiligung Hyperkalziurie, idiopathische Okulo-reno-zerebelläres Syndrom, schweres Glomerulonephritis, membranoproliferative, Immunoglobulin-vermittelte Hyperurikämie-pulmonale Hypertension- Nierenversagen-Alkalose-Syndrom RHYNS-Syndrom Glomerulonephritis, membranoproliferative, nicht Immunoglobulin-vermittelte Primäre Hypomagnesiämie mit sekundärer Hypokalzämie C3-Glomerulonephritis Zystinurie Polyangiitis, mikroskopische Nierenkrankheit, polyzystische, autosomal-dominante Nierenkrankheit, polyzystische, autosomal-rezessive Denys-Drash-Syndrom Hypomagnesiämie, primäre, genetisch bedingte Diabetes insipidus, nephrogener Nierenkrankheit, tubulointerstitielle, autosomal-dominante, REN-assoziierte Pseudohypoaldosteronismus Typ 1 Lipoprotein-Glomerulopathie Joubert-Syndrom mit okulo-renalem Defekt Neugeborenen-Diabetes - kongenitale Hypothyreose - kongenitales Glaukom - Leberfibrose - polyzystische Nieren Nephrotisches Syndrom, idiopathisches steroid-resistentes, mit kollabierende Glomerulopathie, sporadische Form Nephrotisches Syndrom, infantiles kongenitales MYH9-assoziierte Krankheiten Mikroangiopathie, thrombotische, genetisch bedingte Nephrotisches Syndrom, idiopathisches steroid-resistentes, sporadisches Pseudohypoparathyreoidismus Familiäre Hypomagnesiämie mit Hyperkalziurie und Nephrokalzinose ohne schwere Augenbeteiligung Interstitielle Lungenkrankheit-Nephrotisches Syndrom-Epidermolysis bullosa-Syndrom LAMB2-assoziiertes nephrotisches Syndrom mit Beginn im Kindesalter Familiäre primäre Hypomagnesiämie mit Hyperkalziurie und Nephrokalzinose Primäre Hypomagnesiämie mit Hypokalziurie, genetisch bedingte Frasier-Syndrom Nierenkrankheit, polyzystische, autosomal-dominante, Typ 1, mit tuberöser Sklerose Hypomagnesiämie mit Normokalziurie, genetisch bedingte Pseudohypoparathyreoidismus ohne Albright'sche hereditäre Osteodystrophie Nierenkrankheit, tubulointerstitielle, autosomal-dominante Gitelman-Syndrom Hypotonie-Cystinurie-Syndrom Pseudohypoaldosteronismus Typ 2A Basalmembrandefekt Mikrodeletionssyndrom 2p21 Aktionsmyoklonus-Nierenversagen-Syndrom Nierenerkrankung, tubulointerstitielle, autosomal-dominante, MUC1-assoziierte Nierenerkrankung, tubulointerstitielle, autosomal-dominante, UMOD-assoziierte WAGR-Syndrom Glomerulonephritis, membranoproliferative, Typ 2 Pseudohypoparathyreoidismus Typ 1B Hypourikämie, hereditäre renale Xanthinurie, hereditäre Pseudohypoparathyreoidismus Typ 2 Atypisches hämolytisch-urämische Syndrom mit I-Faktor-Anomalie Zystische Nierenerkrankung, genetisch bedingte Nephronophthise, infantile Form Nephronophthise, juvenile Form Psychomotorische Regression-okulomotorische Apraxie-Bewegungsstörung-Nephropathie-Syndrom Hyperoxalurie, primäre, Typ 1 Xanthinurie Typ I Hyperoxalurie, primäre Hyperoxalurie, primäre, Typ 3 Xanthinurie Typ II Bartter-Syndrom Typ 3 Bartter-Syndrom, pränatales Autosomal recessive proximal renal tubular acidosis Nephrogenic syndrome of inappropriate antidiuresis Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation Autosomal dominant distal renal tubular acidosis Cystinuria type B Cystinuria type A Renal dysplasia Dent disease type 2 Hypotonia-cystinuria type 1 syndrome Dent disease type 1 Atypical hypotonia-cystinuria syndrome Atypical hemolytic uremic syndrome with thrombomodulin anomaly Primary renal tubular acidosis Idiopathic steroid-sensitive nephrotic syndrome Adenine phosphoribosyltransferase deficiency Familial juvenile hyperuricemic nephropathy type 1 Primary glomerular disease Pseudohypoaldosteronism type 2D Infantile nephropathic cystinosis Hepatic fibrosis-renal cysts-intellectual disability syndrome Juvenile nephropathic cystinosis Renal dysplasia, bilateral Renal dysplasia, unilateral Pseudohypoaldosteronism type 2E X-linked Alport syndrome-diffuse leiomyomatosis Rapidly progressive glomerulonephritis Unspecified juvenile idiopathic arthritis Autosomal recessive infantile hypercalcemia Mevalonic aciduria Proximal renal tubular acidosis Dominant hypophosphatemia with nephrolithiasis or osteoporosis Pseudopseudohypoparathyroidism Polyarticular juvenile idiopathic arthritis Megacystis-microcolon-intestinal hypoperistalsis syndrome Pseudohypoaldosteronism type 2 Rare pediatric vasculitis Type 1 interferonopathy of childhood Psoriasis-related juvenile idiopathic arthritis Nephronophthisis Hemolytic uremic syndrome with DGKE deficiency Isolated autosomal dominant hypomagnesemia, Glaudemans type Fetal lower urinary tract obstruction Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome Familial primary hypomagnesemia with normocalciuria and normocalcemia Autosomal dominant primary hypomagnesemia with hypocalciuria Osteopetrosis with renal tubular acidosis Bartter syndrome with hypocalcemia Rare genetic renal disease Primary Fanconi renotubular syndrome Genetic renal tubular disease Multicystic dysplastic kidney Congenital nephrotic syndrome, Finnish type Familial steroid-resistant nephrotic syndrome with sensorineural deafness Bartter syndrome type 4 X-linked Alport syndrome Autosomal recessive Alport syndrome Autosomal dominant Alport syndrome Renal pseudohypoaldosteronism type 1 Pseudohypoparathyroidism with Albright hereditary osteodystrophy Generalized pseudohypoaldosteronism type 1 Pseudohypoaldosteronism type 2B Pseudohypoaldosteronism type 2C Atypical hemolytic uremic syndrome with C3 anomaly Atypical hemolytic uremic syndrome with MCP/CD46 anomaly Atypical hemolytic uremic syndrome with H factor anomaly Atypical hemolytic uremic syndrome with B factor anomaly Atypical hemolytic uremic syndrome with anti-factor H antibodies Congenital thrombotic thrombocytopenic purpura Late-onset nephronophthisis Nephropathy secondary to a storage or other metabolic disease Prune belly syndrome Primary hyperoxaluria type 2 Distal renal tubular acidosis with anemia Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Renal coloboma syndrome Familial steroid-resistant nephrotic syndrome with adrenal insufficiency