U.S. ICD-10-CM reference · FY2026 · April
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N07Kategori · daha fazla ayrıntı gerekliArşiv

Hereditary nephropathy, not elsewhere classified

HiyerarşiN00-N08 · N07

Kod talimatları

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

Üst düzey talimatlar

Bölümler 14 · Diseases of the genitourinary system (N00-N99)

Excludes 2
  • certain conditions originating in the perinatal period (P04-P96)
  • certain infectious and parasitic diseases (A00-B99)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)
  • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • endocrine, nutritional and metabolic diseases (E00-E88)
  • injury, poisoning and certain other consequences of external causes (S00-T88)
  • neoplasms (C00-D49)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)

N00-N08 · Glomerular diseases (N00-N08)

Excludes 1

hypertensive chronic kidney disease (I12.-)

Code also

any associated kidney failure (N17-N19).

Daha ayrıntılı kodlar

N07.0Hereditary nephropathy, not elsewhere classified with minor glomerular abnormalityFaturalandırılabilir, belirli kodN07.1Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesionsFaturalandırılabilir, belirli kodN07.2Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritisFaturalandırılabilir, belirli kodN07.3Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritisFaturalandırılabilir, belirli kodN07.4Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritisFaturalandırılabilir, belirli kodN07.5Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritisFaturalandırılabilir, belirli kodN07.6Hereditary nephropathy, not elsewhere classified with dense deposit diseaseFaturalandırılabilir, belirli kodN07.7Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritisFaturalandırılabilir, belirli kodN07.8Hereditary nephropathy, not elsewhere classified with other morphologic lesionsFaturalandırılabilir, belirli kodN07.9Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesionsFaturalandırılabilir, belirli kodN07.AHereditary nephropathy, not elsewhere classified with C3 glomerulonephritisFaturalandırılabilir, belirli kodN07.BHereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]Faturalandırılabilir, belirli kod
Kod sürümü