MCMedicalCodingSoftware
N07.B

N07.B: Hereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]

Billable / specific codeICD-10-CM

N07.B is a billable, specific ICD-10-CM code for hereditary nephropathy, not elsewhere classified with apol1-mediated kidney disease [amkd]. It is valid for submission on a claim.

Check N07.B with the rest of the claim: free scrubber

Inclusion terms

Alternative wordings a physician may use in the chart for this same code.

  • AMKD (with glomerulonephritis)
  • AMKD (with glomerulosclerosis)

Excludes2 inherited from the categories above N07.B

Not part of this code, but both may be coded when both are present.

Written on N07: Hereditary nephropathy, not elsewhere classified

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

Risk adjustment

No CMS-HCC V28 category: this code does not change a RAF score.

Alphabetic index entries that lead here

  • AMKD(APOL1-mediated kidney disease) (with glomerulonephritis) (with glomerulosclerosis)
  • Nephropathy›hereditary NEC›with›APOL1-mediated kidney disease(AMKD)

Code history

  • addedFY2024-FY2027

    Hereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]

Other codes under N07

ICD-10-CMFY2027· effective October 1, 2026

Loaded directly from the CMS/NCHS ICD-10-CM public-domain release: see data sources and our editorial policy. If this page disagrees with the CMS tabular list, this page is wrong. Reference information for professional coders; not medical or billing advice.