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nephropathy, not elsewhere classified with focal and segmental hyalinosis
- Hereditary nephropathy, not elsewhere classified with focal and segmental sclerosis
- Hereditary nephropathy, not elsewhere classified with focal glomerulonephritis
- N07.2 Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis
- N07.3 Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis
- N07.4 Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
- N07.5 Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis
- Hereditary nephropathy, not elsewhere classified with membranoproliferative glomerulonephritis, types 1 and 3, or NOS
- N07.6 Hereditary nephropathy, not elsewhere classified with dense deposit disease
- Hereditary nephropathy, not elsewhere classified with membranoproliferative glomerulonephritis, type 2
- N07.7 Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis
- Hereditary nephropathy, not elsewhere classified with extracapillary glomerulonephritis
- N07.8 Hereditary nephropathy, not elsewhere classified with other morphologic lesions
- Hereditary nephropathy, not elsewhere classified with proliferative glomerulonephritis NOS
- N07.9 Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions
N08 Glomerular disorders in diseases classified elsewhere
- Includes: glomerulonephritis
- nephritis
- nephropathy
- Code first underlying disease, such as:
- amyloidosis (E85.-)
- congenital syphilis (A50.5)
- cryoglobulinemia (D89.1)
- disseminated intravascular coagulation (D65)
- gout ( M1a-, M10.-)
- microscopic polyangiitis (M31.7)
- multiple myeloma (C90.0-)
- sepsis (A40.0-A41.9)
- sickle-cell disease (D57.0-D57.8)
- Excludes1: glomerulonephritis, nephritis and nephropathy (in):
- antiglomerular basement membrane disease (M31.0)
- diabetes (
