Q61.2 Polycystic kidney, autosomal dominant - analogs
| Description «Q61.2 Polycystic kidney, autosomal dominant» | ||||||
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- 50% Compare Q61.3 Polycystic kidney, unspecified
- 36% Compare Q61.1 Polycystic kidney, autosomal recessive
- 20% Compare N20 Calculus of kidney and ureter
- 20% Compare N20.2 Calculus of kidney with calculus of ureter
- 16% Compare N22 Calculus of urinary tract in diseases classified elsewhere
- 16% Compare N22.8 Calculus of urinary tract in other diseases classified elsewhere
- 16% Compare N25.0 Renal osteodystrophy
- 14% Compare N13.2 Hydronephrosis with renal and ureteral calculous obstruction
- 12% Compare N20.0 Calculus of kidney
- 10% Compare N00.7 Acute nephritic syndrome, diffuse crescentic glomerulonephritis
- 10% Compare I13 Hypertensive heart and renal disease
- 10% Compare I13.9 Hypertensive heart and renal disease, unspecified
- 10% Compare N04.2 Nephrotic syndrome, diffuse membranous glomerulonephritis
- 10% Compare I13.1 Hypertensive heart and renal disease with renal failure
- 10% Compare N07.5 Hereditary nephropathy, not elsewhere classified, diffuse mesangiocapillary glomerulonephritis
- 10% Compare N07.7 Hereditary nephropathy, not elsewhere classified, diffuse crescentic glomerulonephritis
- 10% Compare I12 Hypertensive renal disease
- 10% Compare N00.5 Acute nephritic syndrome, diffuse mesangiocapillary glomerulonephritis
- 10% Compare N00.4 Acute nephritic syndrome, diffuse endocapillary proliferative glomerulonephritis
- 10% Compare N07.4 Hereditary nephropathy, not elsewhere classified, diffuse endocapillary proliferative glomerulonephritis
- 10% Compare N00.3 Acute nephritic syndrome, diffuse mesangial proliferative glomerulonephritis
- 10% Compare N07.3 Hereditary nephropathy, not elsewhere classified, diffuse mesangial proliferative glomerulonephritis
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