SE-ATLAS

Undifferentiated connective tissue syndrome Secondary glomerular disease IgG4-related kidney disease Giant cell arteritis Pediatric systemic lupus erythematosus Oculocerebrorenal syndrome of Lowe Satoyoshi syndrome Joubert syndrome with oculorenal defect Adrenocortical carcinoma Systemic sclerosis Juvenile polymyositis Pseudohypoaldosteronism Anaplastic thyroid carcinoma Nephrogenic diabetes insipidus-intracranial calcification-short stature-facial dysmorphism syndrome Neonatal severe primary hyperparathyroidism Differentiated thyroid carcinoma Secondary vasculitis Thrombotic microangiopathy Systemic autoimmune disease Atypical hemolytic uremic syndrome with MCP/CD46 anomaly Atypical hemolytic uremic syndrome with C3 anomaly Genetic renal tubular disease Atypical hemolytic uremic syndrome with H factor anomaly Takayasu arteritis Atypical hemolytic uremic syndrome with B factor anomaly Idiopathic hypercalciuria Dent disease Autosomal systemic lupus erythematosus Atypical hemolytic uremic syndrome with anti-factor H antibodies Cranioectodermal dysplasia Atypical hemolytic uremic syndrome with I factor anomaly Senior-Loken syndrome Genetic primary hypomagnesemia Susac syndrome IgG4-related disease Shiga toxin-associated hemolytic uremic syndrome Genetic cystic renal disease Atypical hemolytic uremic syndrome with thrombomodulin anomaly Nail-patella syndrome Familial primary hyperparathyroidism Dominant hypophosphatemia with nephrolithiasis or osteoporosis Primary renal tubular acidosis Hypophosphatemic rickets Nephropathy secondary to a storage or other metabolic disease PLCG2-associated antibody deficiency and immune dysregulation Simple cryoglobulinemia VIPoma Nephrogenic syndrome of inappropriate antidiuresis Familial papillary thyroid carcinoma with renal papillary neoplasia Relapsing polychondritis Cystinuria type B Cystinuria type A Polymyositis Genetic hyperparathyroidism Rare genetic cause of hypertension Mitochondrial DNA depletion syndrome, hepatocerebrorenal form Familial nonmedullary thyroid carcinoma Primary Fanconi renotubular syndrome Alström syndrome Multiple endocrine neoplasia type 4 Senior-Boichis syndrome Multiple endocrine neoplasia Multiple endocrine neoplasia type 2A Multiple endocrine neoplasia type 2B Jeune syndrome Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome Pseudohypoparathyroidism EAST syndrome Hemolytic uremic syndrome with DGKE deficiency Congenital renal artery stenosis IgG4-related retroperitoneal fibrosis Cystinuria Overlapping connective tissue disease Saldino-Mainzer-Syndrom Glomerulopathie, primäre Antisynthetase-Syndrom RHYNS-Syndrom Gitelman-Syndrom Cushing-Syndrom, ACTH-unabhängiges Cushing-Syndrom durch ektopische ACTH-Produktion Seltene Krankheit mit Cushing-Syndrom als Hauptmerkmal Cushing-Syndrom durch bilaterale makronoduläre Nebennierenhyperplasie Adrenales Cushing-Syndrom Dermatomyositis HNF1B-assoziierte autosomal-dominante tubulointerstitielle Nierenerkrankung Evans-Syndrom mit assoziiertem primären Immundefekt Vaskulitis, unklassifizierte Cushing-Krankheit Reynolds-Syndrom Hypotonie-Cystinurie-Syndrom Typ 1 Schilddrüsenkarzinom, medulläres Neoplasie, endokrine multiple, Typ 1 Neoplasie, endokrine multiple, Typ 2 Dermatomyositis, juvenile Nephronophthise Autoimmunkrankheit, multisystemische syndromale, durch Itch-Mangel Vaskulitis großer Gefäße Bartter-Syndrom Vaskulitis Vaskulitis kleiner Gefäße Hypourikämie, hereditäre renale Vaskulitis mittelgroßer Gefäße Seltenes Schilddrüsenkarzinom Sarkoidose Behçet-Syndrom Tubulointerstitielle Nephritis und Uveitis-Syndrom Cushing-Syndrom, endogenes Nierenkrankheit, tubulointerstitielle, autosomal-dominante, REN-assoziierte Cushing-Syndrom, ACTH-abhängiges Hämolytisch-urämisches Syndrom, atypische Form Autoimmune interstitielle Lungenerkrankung-Arthritis-Syndrom Polyangiitis, mikroskopische Diabetes insipidus, nephrogener Sekundäre neonatale autoimmune Krankheit Mischkollagenose Sjögren-Larsson-Syndrom Glomerulopathie Basalmembrandefekt Granulomatose mit Polyangiitis STAT3-assoziierte früh beginnende multisystemische Autoimmunkrankheit Prolaktinom Seltene renal-tubuläre Funktionsstörung Seltene Ursache der Hypertension