SE-ATLAS

Glomerulopathie Undifferenzierte Kollagenosen Glomerulopathie, sekundäre Basalmembrandefekt IgG4-assoziierte Nierenkrankheit Riesenzell-Arteriitis Lupus erythematodes, systemischer, des Kindesalters Okulo-zerebro-renales Syndrom Lowe Mischkollagenose Satoyoshi-Syndrom Sjögren-Larsson-Syndrom Joubert-Syndrom mit okulo-renalem Defekt Adrenokortikales Karzinom Systemische Sklerodermie Polymyositis, juvenile Pseudohypoaldosteronismus Autoimmune interstitielle Lungenerkrankung-Arthritis-Syndrom Schilddrüsenkarzinom, anaplastisches Nephrogener Diabetes insipidus-intrakranielle Kalzifikation-Kleinwuchs-Gesichtsdysmorphie-Syndrom Hyperparathyroidismus, neonataler primärer schwerer Schilddrüsenkarzinom, differenziertes Vaskulitis, sekundäre Mikroangiopathie, thrombotische Autoimmune Krankheit, systemische Atypisches hämolytisch-urämische Syndrom mit MCP- oder CD46-Anomalie Atypisches hämolytisch-urämische Syndrom mit C3-Anomalie Renal-tubuläre Störung, genetisch bedingte Atypisches hämolytisch-urämische Syndrom mit H-Faktor-Anomalie Takayasu-Arteriitis Atypisches hämolytisch-urämische Syndrom mit B-Faktor-Anomalie Hyperkalziurie, idiopathische Atypisches hämolytisch-urämische Syndrom mit anti-Faktor H-Antikörpern Dysplasie, kranioektodermale Lupus erythematodes, systemischer, autosomal-rezessiver Dent-Krankheit Atypisches hämolytisch-urämische Syndrom mit I-Faktor-Anomalie Senior-Loken-Syndrom Susac-Syndrom Hypomagnesiämie, primäre, genetisch bedingte IgG4-assoziierte Krankheit Shiga-ähnliches Toxin-assoziiertes Hämolytisch-urämisches Syndrom Atypisches hämolytisch-urämische Syndrom mit Thrombomodulin-Anomalie Zystische Nierenerkrankung, genetisch bedingte Nagel-Patella-Syndrom Hyperparathyreoidismus, familiärer primärer Dominante Hypophosphatämie mit Nephrolithiasis oder Osteoporose Azidose, renale tubuläre, primäre Hypophosphatämische Rachitis 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