Specific

2,8-dihydroxyadenuria adult polycystic kidney disease; autosomal dominant polycystic kidney disease Alport syndrome; hereditary nephropathy autosomal dominant distal renal tubular acidosis autosomal recessive distal renal tubular acidosis Bartter syndrome childhood polycystic kidney disease cystinuria Dent disease complex familial focal segmental glomerulosclerosis familial hypomagnesemia type 3; familial hypomagnesemia with hypercalciuria & nephrocalcinosis (FHHNC) familial juvenile hyperuricemic nephropathy (HNFJ) familial nephrotic syndrome Fechtner syndrome Finnish-type congenital nephropathy Gitelman syndrome glomerulocystic kidney disease Hartnup disease hereditary nephrolithiasis hereditary renal tubular defects hypomagnesemia renal with ocular involvement hypophosphatemic nephrolithiasis/osteoporosis hypophosphatemic nephrolithiasis/osteoporosis type 1 iminoglycinuria infantile polycystic kidney disease (autosomal recessive) isolated diffuse mesangial sclerosis (IDMS) lipoprotein glomerulopathy medullary cystic kidney disease multicystic renal dysplasia (MRD); pelviureteric junctional obstruction (PUJO) nephronophthisis nephropathic cystinosis oligomeganephronia renal aplasia/agenesis renal tubular dysgenesis susceptibility to diabetic nephropathy; susceptibility to microvascular complications of diabetes type 7 (MVCD7); susceptibility to diabetic proliferative retinopathy susceptibility to uric acid nephrolithiasis thin glomerular basement membrane disease; benign familial hematuria xanthinuria

General

chronic kidney disease (CKD) genetic disease