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ICD-10 diagnosis code

N07 Hereditary nephropathy, not elsewhere classified

This page in Swedish

N07 is the ICD-10 code for Hereditary nephropathy, not elsewhere classified. It is a three-character category. WHO defines its fourth-character subdivisions once for the whole group of categories; the national editions below list them in full. It belongs to the block N00–N08 (Glomerular diseases) in Chapter XIV, Diseases of the genitourinary system.

Code type
Category (3 characters)
Chapter
XIV · N00–N99
Classification
WHO ICD-10, 2019 version

What N07 excludes

Conditions that look similar but belong under another code.

  • Alport syndrome Q87.8
  • hereditary amyloid nephropathy E85.0
  • nail patella syndrome Q87.2
  • non-neuropathic heredofamilial amyloidosis E85.0

N07 in national editions

Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.

SwedenICD-10-SE

N07Hereditär nefropati som ej klassificeras på annan plats

  • N07.0Hereditär nefropati som ej klassificeras på annan plats - lätt glomerulär abnormitet
  • N07.1Hereditär nefropati som ej klassificeras på annan plats - fokala och segmentella glomerulära skador
  • N07.2Hereditär nefropati som ej klassificeras på annan plats - diffus membranös glomerulonefrit
  • N07.3Hereditär nefropati som ej klassificeras på annan plats - diffus mesangiell proliferativ glomerulonefrit
  • N07.4Hereditär nefropati som ej klassificeras på annan plats - diffus endokapillär proliferativ glomerulonefrit
  • N07.5Hereditär nefropati som ej klassificeras på annan plats - diffus mesangiokapillär glomerulonefrit
  • N07.6Hereditär nefropati som ej klassificeras på annan plats - dense deposit disease
  • N07.7Hereditär nefropati som ej klassificeras på annan plats - diffus crescentisk glomerulonefrit
  • and 2 more national subcodes
NorwayICD-10-NO

Listed through more specific codes:

  • N07.0Arvelig nefropati ikke klassifisert annet sted, med mindre glomerulær abnormitet
  • N07.1Arvelig nefropati ikke klassifisert annet sted, med fokal eller segmentell glomerulusskade
  • N07.2Arvelig nefropati ikke klassifisert annet sted, med diffus membranøs glomerulonefritt
  • N07.3Arvelig nefropati ikke klassifisert annet sted, med diffus mesangiell proliferativ glomerulonefritt
  • N07.4Arvelig nefropati ikke klassifisert annet sted, med diffus endokapillær proliferativ glomerulonefritt
  • N07.5Arvelig nefropati ikke klassifisert annet sted, med diffus mesangiokapillær glomerulonefritt
  • N07.6Arvelig nefropati ikke klassifisert annet sted, med «dense deposit disease»
  • N07.7Arvelig nefropati ikke klassifisert annet sted, med diffus halvmåne-glomerulonefritt
  • and 2 more national subcodes
DenmarkICD-10-DK

DN07Arvelig nyresygdom IKA

  • DN070Arvelig nefropati med minimale glomerulære forandringer
  • DN071Arvelig nefropati med fokale eller segmentære glomerulære forandringer
  • DN072Arvelig nefropati med diffus membranøs morfologi
  • DN073Arvelig nefropati med diffus mesangial proliferation
  • DN074Arvelig nefropati med diffus endokapillær proliferation
  • DN075Arvelig nefropati med membranoproliferativ morfologi type 1 og 3 eller UNS
  • DN076Arvelig nefropati med membranoproliferativ morfologi type 2
  • DN077Arvelig nefropati med ekstrakapillær morfologi
  • and 2 more national subcodes
GermanyICD-10-GM

N07Hereditäre Nephropathie, anderenorts nicht klassifiziert

FranceICD-10-FR

N07Néphropathie héréditaire, non classée ailleurs

NetherlandsICD-10-NL

N07hereditaire nefropathie, niet elders geclassificeerd

United StatesICD-10-CM

Listed through more specific codes:

  • N07.0Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality
  • N07.1Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions
  • N07.2Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis
  • N07.3Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis
  • N07.4Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
  • N07.5Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis
  • N07.6Hereditary nephropathy, not elsewhere classified with dense deposit disease
  • N07.7Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis
  • and 4 more national subcodes

Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.

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