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 syndrome Primary glomerular disease Antisynthetase syndrome RHYNS syndrome Gitelman syndrome ACTH-independent Cushing syndrome Cushing syndrome due to ectopic ACTH secretion Rare disease with adrenal Cushing syndrome as a major feature Cushing syndrome due to bilateral macronodular adrenocortical disease Adrenal Cushing syndrome Dermatomyositis HNF1B-related autosomal dominant tubulointerstitial kidney disease Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Unclassified vasculitis Cushing disease Reynolds syndrome Hypotonia-cystinuria type 1 syndrome Medullary thyroid carcinoma Multiple endocrine neoplasia type 1 Multiple endocrine neoplasia type 2 Juvenile dermatomyositis Nephronophthisis Syndromic multisystem autoimmune disease due to Itch deficiency Predominantly large-vessel vasculitis Bartter syndrome Vasculitis Predominantly small-vessel vasculitis Hereditary renal hypouricemia Predominantly medium-vessel vasculitis Rare thyroid carcinoma Sarcoidosis Behçet disease Tubulointerstitial nephritis and uveitis syndrome Endogenous Cushing syndrome REN-related autosomal dominant tubulointerstitial kidney disease ACTH-dependent Cushing syndrome Atypical hemolytic uremic syndrome Autoimmune interstitial lung disease-arthritis syndrome Microscopic polyangiitis Nephrogenic diabetes insipidus Secondary neonatal autoimmune disease Mixed connective tissue disease Sjögren-Larsson syndrome Glomerular disease Basement membrane disease Granulomatosis with polyangiitis STAT3-related early-onset multisystem autoimmune disease Prolactinoma Rare renal tubular disease Rare cause of hypertension