genetic disease of the kidney
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More general terms
More specific terms
- 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