N07.A Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis

Billable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis.

Applicable to

• Hereditary nephropathy, not elsewhere classified with C3 glomerulopathy

Excludes1 (never code together)

• Hereditary nephropathy, not elsewhere classified (with C3 glomerulopathy) with dense deposit disease (N07.6)

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.

Code annotations containing back-references to N07.A

Back-references to N07.A

• Type 1 Excludes: N07.5 Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis ("Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis (N07.A)")
• Type 1 Excludes: N07.5 Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis ("Hereditary nephropathy, not elsewhere classified with C3 glomerulopathy (N07.A)")

Diagnosis Index entries for N07.A

• Nephropathy › hereditary NEC › with › C3 › glomerulonephritis
• Nephropathy › hereditary NEC › with › C3 › glomerulopathy

Nearby codes

• N07.5 Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis
• 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 (this code)
• N07.B Hereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]