N07.2 Hereditary nephropathy, not elsewhere classified, diffuse membranous glomerulonephritis - analogs
| Description «N07.2 Hereditary nephropathy, not elsewhere classified, diffuse membranous glomerulonephritis» | ||||||
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- 42% Compare N07.7 Hereditary nephropathy, not elsewhere classified, diffuse crescentic glomerulonephritis
- 42% Compare N07.3 Hereditary nephropathy, not elsewhere classified, diffuse mesangial proliferative glomerulonephritis
- 42% Compare N07.4 Hereditary nephropathy, not elsewhere classified, diffuse endocapillary proliferative glomerulonephritis
- 42% Compare N07.5 Hereditary nephropathy, not elsewhere classified, diffuse mesangiocapillary glomerulonephritis
- 40% Compare N00.2 Acute nephritic syndrome, diffuse membranous glomerulonephritis
- 34% Compare N04.2 Nephrotic syndrome, diffuse membranous glomerulonephritis
- 25% Compare N00.3 Acute nephritic syndrome, diffuse mesangial proliferative glomerulonephritis
- 25% Compare N00.4 Acute nephritic syndrome, diffuse endocapillary proliferative glomerulonephritis
- 25% Compare N00.5 Acute nephritic syndrome, diffuse mesangiocapillary glomerulonephritis
- 25% Compare N00.7 Acute nephritic syndrome, diffuse crescentic glomerulonephritis
- 20% Compare N04.7 Nephrotic syndrome, diffuse crescentic glomerulonephritis
- 20% Compare N04.4 Nephrotic syndrome, diffuse endocapillary proliferative glomerulonephritis
- 20% Compare N04.3 Nephrotic syndrome, diffuse mesangial proliferative glomerulonephritis
- 20% Compare N04.5 Nephrotic syndrome, diffuse mesangiocapillary glomerulonephritis
- 15% Compare N14.0 Analgesic nephropathy
- 13% Compare N15.0 Balkan nephropathy
- 10% Compare K73.2 Chronic active hepatitis, not elsewhere classified
- 10% Compare K73.8 Other chronic hepatitis, not elsewhere classified
- 10% Compare I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not classified elsewhere
- 10% Compare K73.0 Chronic persistent hepatitis, not elsewhere classified
- 10% Compare K73.1 Chronic lobular hepatitis, not elsewhere classified
- 10% Compare Q61.2 Polycystic kidney, autosomal dominant
- 10% Compare K90.4 Malabsorption due to intolerance, not elsewhere classified
- 10% Compare Q61.3 Polycystic kidney, unspecified
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