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

Billable ICD-10-CM code, FY2026.

Applicable to

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

Applies from N07 Hereditary nephropathy, not elsewhere classified

Excludes2 (not included here)

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

MS-DRG index

Defines the logic of DRG(s) 698-700 in MDC 11.

Diagnosis Index entries for N07.B

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

Nearby codes

• N07.6 Hereditary nephropathy, not elsewhere classified with dense deposit disease
• N07.7 Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis
• N07.8 Hereditary nephropathy, not elsewhere classified with other morphologic lesions
• N07.9 Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions
• N07.A Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis
• N07.B Hereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD] (this code)