U.S. ICD-10-CM reference · FY2026 · April
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N07Kategorie · weitere Spezifizierung erforderlichArchiviert

Hereditary nephropathy, not elsewhere classified

HierarchieN00-N08 · N07

Hinweise zum Code

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

Hinweise übergeordneter Ebenen

Kapitel 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).

Spezifischere Codes

N07.0Hereditary nephropathy, not elsewhere classified with minor glomerular abnormalityAbrechenbarer, spezifischer CodeN07.1Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesionsAbrechenbarer, spezifischer CodeN07.2Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritisAbrechenbarer, spezifischer CodeN07.3Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritisAbrechenbarer, spezifischer CodeN07.4Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritisAbrechenbarer, spezifischer CodeN07.5Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritisAbrechenbarer, spezifischer CodeN07.6Hereditary nephropathy, not elsewhere classified with dense deposit diseaseAbrechenbarer, spezifischer CodeN07.7Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritisAbrechenbarer, spezifischer CodeN07.8Hereditary nephropathy, not elsewhere classified with other morphologic lesionsAbrechenbarer, spezifischer CodeN07.9Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesionsAbrechenbarer, spezifischer CodeN07.AHereditary nephropathy, not elsewhere classified with C3 glomerulonephritisAbrechenbarer, spezifischer CodeN07.BHereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]Abrechenbarer, spezifischer Code
Codeausgabe