SE-ATLAS

Congenital disorder of glycosylation with nephropathy as a major feature Enamel-renal syndrome Primary Fanconi renotubular syndrome Hereditary leiomyomatosis and renal cell cancer Bartter syndrome type 5 Autosomal dominant proximal renal tubular acidosis Joubert syndrome with oculorenal defect Liddle syndrome Galloway-Mowat syndrome Imerslund-Gräsbeck syndrome Oculocerebrorenal syndrome of Lowe Systemic lupus erythematosus Medullary sponge kidney Tuberous sclerosis complex Nail-patella syndrome Multicystic dysplastic kidney Renal agenesis Congenital renal artery stenosis Alport syndrome Alström syndrome Apparent mineralocorticoid excess Fabry disease Familial vesicoureteral reflux Joubert syndrome with renal defect Bartter syndrome type 4 Senior-Loken syndrome Hypertension due to gain-of-function mutations in the mineralocorticoid receptor Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation Frasier syndrome Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis Immunoglobulin A nephropathy Primary membranoproliferative glomerulonephritis Autosomal dominant tubulointerstitial kidney disease Familial hyperaldosteronism type IV Gitelman syndrome Adult familial nephronophthisis-spastic quadriparesia syndrome Tubulointerstitial nephritis and uveitis syndrome Bardet-Biedl syndrome Pierson syndrome Senior-Boichis syndrome MUC1-related autosomal dominant tubulointerstitial kidney disease UMOD-related autosomal dominant tubulointerstitial kidney disease Vitamin B12-unresponsive methylmalonic acidemia type mut0 Birt-Hogg-Dubé syndrome Fibronectin glomerulopathy Von Hippel-Lindau disease Autosomal recessive distal renal tubular acidosis Hypoxanthine guanine phosphoribosyltransferase partial deficiency Familial hyperaldosteronism type III Congenital thrombotic thrombocytopenic purpura Immune-mediated thrombotic thrombocytopenic purpura Familial hyperaldosteronism type I Familial hyperaldosteronism type II Idiopathic hypercalciuria Severe oculo-renal-cerebellar syndrome Primary hyperoxaluria type 1 Primary hyperoxaluria type 3 Bartter syndrome type 3 Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation Immunoglobulin-mediated membranoproliferative glomerulonephritis Cystinuria type B Renal hypoplasia Bartter syndrome type 1 Atypical hemolytic uremic syndrome with anti-factor H antibodies Hereditary pheochromocytoma-paraganglioma Genetic steroid-resistant nephrotic syndrome Late-onset nephronophthisis Hemolytic uremic syndrome with DGKE deficiency Juvenile nephronophthisis Primary hyperoxaluria type 2 Collecting duct carcinoma Fetal lower urinary tract obstruction Autosomal recessive proximal renal tubular acidosis Autosomal dominant distal renal tubular acidosis Saldino-Mainzer syndrome EAST syndrome Cystinuria type A RHYNS syndrome Methylmalonic acidemia with homocystinuria, type cblC Renal dysplasia Bartter syndrome type 2 HNF1B-related autosomal dominant tubulointerstitial kidney disease Dent disease type 2 Hypotonia-cystinuria type 1 syndrome Dent disease type 1 Autosomal dominant intermediate Charcot-Marie-Tooth disease type E C3 glomerulopathy Hemolytic uremic syndrome Hereditary papillary renal cell carcinoma Atypical hemolytic uremic syndrome with complement gene abnormality Vitamin B12-unresponsive methylmalonic acidemia type mut- Cystinosis Familial steroid-resistant nephrotic syndrome with adrenal insufficiency Autosomal dominant polycystic kidney disease Denys-Drash syndrome Autosomal recessive polycystic kidney disease Nephrogenic diabetes insipidus REN-related autosomal dominant tubulointerstitial kidney disease Juvenile cataract-microcornea-renal glucosuria syndrome Pseudohypoaldosteronism type 2 Brachydactyly-arterial hypertension syndrome Lesch-Nyhan syndrome