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N07.6

ICD-10-CM 2027 · Billable

Hereditary nephropathy, not elsewhere classified with dense deposit disease

Sibling codes

  • N07.0 – Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality
  • N07.1 – Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions
  • 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
  • N07.7 – Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis
  • N07.8 – Hereditary nephropathy, not elsewhere classified with other morphologic lesions
  • N07.9 – Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions
  • N07.A – Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis
  • N07.B – Hereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]

Inclusion terms

  • Hereditary nephropathy, not elsewhere classified with C3 glomerulopathy with dense deposit disease
  • Hereditary nephropathy, not elsewhere classified with membranoproliferative glomerulonephritis, type 2

Inherited from N07: Hereditary nephropathy, not elsewhere classified

Excludes2

  • Alport's syndrome (Q87.81-)
  • hereditary amyloid nephropathy (E85.-)
  • nail patella syndrome (Q87.2)
  • non-neuropathic heredofamilial amyloidosis (E85.-)

Part of: N07: Hereditary nephropathy, not elsewhere classified