ICD10

ICD-10 Code N07: Hereditary nephropathy, not elsewhere classified

N07 is an ICD-10 diagnosis entry used to group records related to Hereditary nephropathy, not elsewhere classified. You may see this entry in coding references, medical records, or claims workflows when a broader diagnosis category is being reviewed before a more specific code is chosen. ICD-10 entries help standardize how diagnoses are organized for coding, reporting, analytics, and documentation. This code sits within the broader ICD-10 area for Diseases of the genitourinary system (N00-N99).

Reviewed by HealthAssure Clinical TeamUpdated 21 May 2026

What is this code?

ICD-10 entries help standardize how diagnoses are organized for coding, reporting, analytics, and documentation. This code sits within the broader ICD-10 area for Diseases of the genitourinary system (N00-N99).

When is it used?

  • May be used when a clinician documents hereditary nephropathy, not elsewhere classified in a patient's medical record.
  • May appear in hospital records, claims, referrals, and clinical documentation.
  • This code may act more like a grouping or parent code, so a more specific child code may be used in final documentation when available.

What it does not mean

  • A code alone does not explain severity, treatment plan, or outcome.
  • A medical code should not be treated as a substitute for a doctor's diagnosis or advice.
  • This entry may represent a broader category rather than the most specific billable code.

Code hierarchy

chapter
14Diseases of the genitourinary system (N00-N99)
block
N00-N08Glomerular diseases
currentN00-N08

Official coding notes

Excludes2 (may code together if documented)
  • Alport's syndrome (Q87.81-)
  • hereditary amyloid nephropathy (E85.-)
  • nail patella syndrome (Q87.2)
  • non-neuropathic heredofamilial amyloidosis (E85.-)

Where you may see this code

You may see this entry in coding references, medical records, or claims workflows when a broader diagnosis category is being reviewed before a more specific code is chosen.

Related specialists

UrologistGynecologist

Related codes

N07.0Hereditary nephropathy, not elsewhere classified with minor glomerular abnormalitycodeN07.1Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesionscodeN07.2Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritiscodeN07.3Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritiscodeN07.4Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritiscodeN07.5Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritiscodeN07.6Hereditary nephropathy, not elsewhere classified with dense deposit diseasecodeN07.7Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritiscodeN07.8Hereditary nephropathy, not elsewhere classified with other morphologic lesionscodeN07.9Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesionscodeN07.AHereditary nephropathy, not elsewhere classified with C3 glomerulonephritiscodeN07.BHereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]code

Coding guidelines

Compatibility

Legacy code aligns to an official FY 2026 category. Frontend should resolve to the official category page and surface the billable child codes.
Legacy codes
N07
Replacement codes
N07.0 — Hereditary nephropathy, not elsewhere classified with minor glomerular abnormalityN07.1 — Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesionsN07.2 — Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritisN07.3 — Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritisN07.4 — Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritisN07.5 — Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritisN07.6 — Hereditary nephropathy, not elsewhere classified with dense deposit diseaseN07.7 — Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritisN07.8 — Hereditary nephropathy, not elsewhere classified with other morphologic lesionsN07.9 — Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesionsN07.A — Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritisN07.B — Hereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]

Common synonyms

Hereditary nephropathy, not elsewhere classified

Frequently asked questions

Code details

CodeN07
SystemICD10
Display nameHereditary nephropathy, not elsewhere classified
ChapterDiseases of the genitourinary system (N00-N99)
BlockGlomerular diseases

Flags

BillableNo
Valid clinical useNo

Source

SourceICD-10
Version2026-annual
Releaseannual
Year2026

About this content

This page is prepared by HealthAssure's clinical team using official coding standards from ICD-10. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.