SE-ATLAS

Glomerular disease Undifferentiated connective tissue syndrome Secondary glomerular disease Basement membrane disease IgG4-related kidney disease Giant cell arteritis Pediatric systemic lupus erythematosus Oculocerebrorenal syndrome of Lowe Mixed connective tissue disease Satoyoshi syndrome Sjögren-Larsson syndrome Joubert syndrome with oculorenal defect Adrenocortical carcinoma Systemic sclerosis Juvenile polymyositis Pseudohypoaldosteronism Autoimmune interstitial lung disease-arthritis syndrome 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 Atypical hemolytic uremic syndrome with anti-factor H antibodies Cranioectodermal dysplasia Autosomal systemic lupus erythematosus Dent disease Atypical hemolytic uremic syndrome with I factor anomaly Senior-Loken syndrome Susac syndrome Genetic primary hypomagnesemia IgG4-related disease Shiga toxin-associated hemolytic uremic syndrome Atypical hemolytic uremic syndrome with thrombomodulin anomaly Genetic cystic renal disease 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 Rare renal tubular disease Nephrogenic syndrome of inappropriate antidiuresis Familial papillary thyroid carcinoma with renal papillary neoplasia Microscopic polyangiitis Relapsing polychondritis Cystinuria type B Cystinuria type A Polymyositis Fabry disease Genetic hyperparathyroidism Rare genetic cause of hypertension Rare cause of hypertension REN-related autosomal dominant tubulointerstitial kidney disease Mitochondrial DNA depletion syndrome, hepatocerebrorenal form Familial nonmedullary thyroid carcinoma Primary Fanconi renotubular syndrome Alström syndrome Multiple endocrine neoplasia type 4 Jeune syndrome Multiple endocrine neoplasia Senior-Boichis syndrome Multiple endocrine neoplasia type 2A Multiple endocrine neoplasia type 2B Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome STAT3-related early-onset multisystem autoimmune disease Pseudohypoparathyroidism EAST syndrome Hemolytic uremic syndrome with DGKE deficiency Congenital renal artery stenosis IgG4-related retroperitoneal fibrosis Overlapping connective tissue disease Cystinuria Saldino-Mainzer syndrome Primary glomerular disease Antisynthetase syndrome Granulomatosis with polyangiitis RHYNS syndrome Gitelman syndrome ACTH-independent Cushing syndrome Nephrogenic diabetes insipidus Atypical hemolytic uremic syndrome Rare disease with adrenal Cushing syndrome as a major feature Cushing syndrome due to ectopic ACTH secretion ACTH-dependent Cushing syndrome Endogenous Cushing syndrome Cushing syndrome due to bilateral macronodular adrenocortical disease Dermatomyositis Adrenal Cushing syndrome HNF1B-related autosomal dominant tubulointerstitial kidney disease Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Unclassified vasculitis Secondary neonatal autoimmune disease Cushing disease Reynolds syndrome Prolactinoma Hypotonia-cystinuria type 1 syndrome Medullary thyroid carcinoma Multiple endocrine neoplasia type 1 Juvenile dermatomyositis Multiple endocrine neoplasia type 2 Nephronophthisis Predominantly large-vessel vasculitis Syndromic multisystem autoimmune disease due to Itch deficiency Bartter syndrome Predominantly small-vessel vasculitis Vasculitis Hereditary renal hypouricemia Predominantly medium-vessel vasculitis Rare thyroid carcinoma Sarcoidosis Behçet disease Tubulointerstitial nephritis and uveitis syndrome