Genetic Disease Of The Kidney
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More Specific Terms
- 2,8-dihyroxyadenuria
- adult polycystic kidney disease
- Alport syndrome
- autosomal dominant distal renal tubular acidosis
- autosomal recessive distal renal tubular acidosis
- Bartter syndrome
- benign familial hematuria; thin basement membrane nephropathy
- 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
- Gitelman syndrome
- glomerulocystic kidney disease
- Hartnup disease
- hereditary nephrolithiasis
- hereditary renal tubular defects
- hyperoxaluria
- hypomagnesemia renal with ocular involvement
- hypophosphatemic nephrolithiasis/osteoporosis
- hypophosphatemic nephrolithiasis/osteoporosis type 1
- iminoglycinuria
- infantile polycystic kidney disease
- isolated diffuse mesangial sclerosis (IDMS)
- medullary cystic kidney disease
- multicystic renal dysplasia (MRD); pelviureteric junctional obstrucion (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
- xanthinuria
More General Terms
